Cell sensitivity, non-linearity and inverse effects

Figure 1. Allosteric and orthosteric drug actions. Allosteric (A) and orthosteric (O) regulation of different macromolecules. A: Enzymes; B: Cell receptors; D: Membrane channels and transport mechanisms; E: Gene expression at the promoter site.

Introduction
According to the ‘similarity’ (or ‘similia’) principle, patients can be cured using low doses or high dilutions/dynamizations of a drug that in healthy people produces similar symptoms to the disease. However, this approach is regarded as unscientific by some circles.1, 2 One current opinion about homeopathic treatment associates this medical approach with the placebo effect, either because of some highly publicized meta-analysis3 or because of the alleged implausibility of its theories.4, 5, 6 While controversies concerning the clinical efficacy have been recently discussed by others,7 here we survey the homeopathic basic principles with the aim of examining their consistency with modern scientific knowledge of biological communication at cellular and molecular levels. The low dose effects and the healing power of pathogenic substances observed in homeopathy, are linked to the high sensitivity of biological systems at various levels of organization and to the multiform ways through which the complex of mind-body homeodynamic regulations (‘vital force’) reacts to external stimuli. Growing evidence from several science fields suggests that hormesis and paradoxical pharmacology are included in the ‘adaptation’ capacity of immune, neuroendocrine and cardiovascular systems, but also in cellular defence/repair mechanisms and even in molecular dynamics and conformational changes.8, 9, 10, 11, 12, 13, 14, 15

Our working hypothesis is that recognition of the function of enzymes, receptors and signal transduction and their dynamic interaction with drugs, makes it possible to look at homeopathy in a new and fully rational light. The cornerstone of homeopathy – that the whole clinical picture of the individual patient to be taken into consideration – is not in dispute, but laboratory models also allow the mechanism(s) of action of drugs to be investigated in animals, cells, tissues, and even at the molecular level. This ‘reductionistic’ perspective is not in contrast with the ‘holistic’ approach of homeopathy as a healing system, but rather represents the fundamental basis of a developing theory which would include recent advancements in complexity science and systems biology.15, 16, 17 Given the holographic and fractal nature of all complex systems, the fundamental characteristics and rules of biological responses and related pathologies can be unravelled at any level of nature.

A glossary of the terms used is given in Table 1.

Table 1
Glossary of the terms utilized
Subject/Term Definition
Abscopal effect A phenomenon sometimes observed in the treatment of tumours: The localized treatment causes not only a shrinking of the treated tumour but also a shrinking of tumours in different compartments.
Allosteric regulation The regulation of a protein by binding a molecule at a site other than the protein’s active site. Allosteric sites allow effectors to bind to the protein, often resulting in a conformational change. The term comes from the Greek allos (ἄλλoς), ‘other,’ and stereos (στɛρɛὀς), ‘solid (object).’
Clathrates The term, from the Latin ‘clathrus’ (= lattice or grating), denotes hollow formations in which the guest molecule is in a cage formed by the host molecule or by a lattice of host molecules. The cage is held together by very weak forces like hydrogen bonding, ion pairing, dipole–dipole interaction and van der Waals attraction.
Desensitization Loss of responsiveness to the continuing or increasing dose of the same factor (agonist, antagonist, drug).
DNA microarray Also commonly known as DNA chip or biochip, is a collection of microscopic DNA spots attached to a solid surface. Scientists use microarrays to measure the expression levels of large numbers of genes simultaneously or to genotype multiple regions of a genome.
Dynamization In homeopathic pharmacopoeia, the dilution process is followed by vigorous shaking (see ‘succussion’) which is believed to provide the remedy with higher pharmacological power.
Energy landscape A mapping of all possible conformations of a molecular entity, or the spatial positions of interacting molecules in a system, and their corresponding free energy levels. While a protein can theoretically exist in a nearly infinite number of conformations along its energy landscape, in reality proteins fold (or ‘relax’) into secondary and tertiary structures that possess the lowest possible free energy.
Epigenetic regulation Functionally relevant changes to the genome that do not involve a change in the nucleotide sequence. Examples of mechanisms that produce such changes are DNA methylation and histone modification, each of which alters how genes are expressed without altering the underlying DNA sequence.
G protein-coupled receptors (GPCRs) Large family of transmembrane receptors that sense molecules outside the cell (odours, pheromones, hormones, and neurotransmitters) and activate inside signals as cyclic-AMP and phosphatidylinositol. When a ligand binds to the GPCR it causes a conformational change, which activates an associated G protein by exchanging its bound GDP for a GTP. The protein chain passes through the cell membrane seven times.
Heat shock proteins A group of proteins induced by heat shock, toxins or other stress (UV radiation, hypoxia). The most prominent members of this group are a class of functionally related proteins involved in the folding and unfolding of other proteins.
Hormesis A phenomenon characterized by low dose stimulation, high dose inhibition of a biological system exposed to toxins and other stressors, resulting in an inverted U-shaped dose response curve.
Metallothioneins A family of cysteine-rich proteins that have the capacity to bind both physiological (such as zinc, copper, selenium) and xenobiotic (such as cadmium, mercury, silver, arsenic) heavy metals
Nanoparticle A small particle composed by one or more compounds, including linked water, measuring 100 nm or less. Nanoparticulate matter has different properties from its bulk form in terms of mechanical, optical, electrical, magnetic, chemical, biological, and quantum behaviours. Nanoparticles cross membranes easily and act as highly reactive and catalytic agents.
Orthosteric site Describing the primary, unmodulated binding site (on a protein) of a ligand. Orthosteric drugs usually block the active site of enzymes and receptors.
Paradoxical pharmacology Term to refer to intriguing observations that chronic use of some drug types can have the opposite biological effect(s) to those seen following acute administration of the same drug.
Priming A memory effect in which exposure to one stimulus influences a response to another stimulus. It may be homologous (same stimulus) or heterologous (two different stimuli).
State-space In the theory of dynamical systems, is the set of values which a process can take. In physics, is an abstract space in which different ‘positions’ represent, not literal locations, but rather states of some physical system. When considering protein folding and free energy, this makes an energy landscape.

Cell sensitivity to ultra-low doses
The cell is the elementary particle of life and its sensitivity to external perturbations is the basis of both pathologic changes and therapeutic interventions. These changes at cellular level can be reduced to three dimensions: stimulation, inhibition, or differentiation. The higher the sensitivity to a regulatory factor – of a chemical, physical, or biological nature – the lower the dose or the energy capable of some ‘effect’. The effects of homeopathic remedies in cellular models are well documented for a wide range of dilutions/dynamizations (Table 2).

Table 2
Effects of increasing dilutions/dynamizations (potencies) in cellular models in vitro, published in peer-reviewed literature
Potencies Test compound Concentration of active principle Cell type Effect
Mother tincture Phytolacca dec.18, 19 Not reported Melanoma, breast carcinoma ↑ Cytotoxicity
Mother tincture Apis mell.20 Not reported Human prostate RWPE-1 ↑↓ expression of different groups of genes (whole genome analysis)
Mother tincture Ruta grav.21 16 mg/ml Dalton’s lymphoma ascites (DLA), Ehrlich ascites carcinoma ↑ Cytotoxicity
Mother tincture Carcinosinum22 Not reported DLA cells ↑ specific gene expression (p53 pro-apoptotic)
1M Thuja23 10−3 of MT DLA cells ↑↓Gene expression (whole genome analysis)
4X Podophyllum24 10−7 Mol/L (podophyllotoxin) Human neutrophils ↑ free radicals production

↓ Adhesion
4X–6X (complex) Arnica, Calendula, Hypericum and Symphytum25 Not reported 3T3 fibroblasts ↑ Cell movement, chemotaxis
6X–12X (complex) Calcium fluor., Magnesium phos., Acidum silicicum26, 27 10−7 Mol/L (fluoride) Rat osteoblasts ↑ Osteogenesis
2C Histamine28, 29 10−4 Mol/L Human basophils ↓↓ CD203c expression
2C Gelsemium s.30, 31 10−9 Mol/L (gelsemine) Human neurocytes SHSY5Y ↓↓ Gene expression (whole genome analysis, RT-array)
2C Gelsemium s.32 Not reported Cervical cancer HeLa ↑ Cytotoxicity
6X Phosphorus, Sulphur33 10−6 Mol/L Human neutrophils ↓ free radicals production
8X Magnesium phos., Manganum phos.33 10−8 Mol/L Human neutrophils ↓ free radicals production
3C, 5C, 7C Apis mell.20 Not reported Human prostate RWPE-1 ↑↓ expression of different groups of genes (whole genome analysis)
5C Gelsemine34 10−10 Mol/L Rat neurons ↑ Neurosteroids
5C Lycopodium clav.35 10−10 of MT Cervical cancer HeLa ↑ Apoptosis
6C Mercurius sol.36 10−16 Mol/L Mice peritoneal macrophages ↑ Interferon-g production

↓ Free radicals production
6C Ruta grav.37 10−12 of MT Cell lines from brain cancer, leukaemia and melanoma ↑ Cytotoxicity in cancer cells (not in normal lymphocytes)
17X Gibberellin38 5×10−18 Mol/L Pea seeds ↑Germination
7X–24X (complex) Acon., Ars., Asa f., Calc. c., Chelid., Cinnamon, Conium, Echinacea, Gelsem., Ipecac., Phos., Rhus t., Thuya, Silicea, and Sulph.39 Not reported HT29 cells, human macrophages ↓NF-κB hyperactivity (reduced expression of reporter gene GFP in transfected HT29 cells), ↓TNF-α release in macrophages
9C Gelsemine34 10−18 Mol/L Rat neurons ↑ Neurosteroids
9C Gelsemium s.30 10−23 Mol/L (gelsemine) Human neurocytes SHSY5Y cell line ↓ Gene expression (whole genome analysis)
10C Triiodothyronine40 10−24 Mol/L Tail cells of Rana ↑ Apoptosis in cells treated with 100 nM T3
10C, 12C Nux vomica or Calendula41 Not reported Human gastric epithelial cell line KATO-III ↓ specific gene expression in H. pylori stimulated HB-EGF gene
15C Lycopodium clav.35 10−30 of MT Cervical cancer HeLa cell line ↑ Apoptosis
30X Rhus tox.42 10−30 of MT Primary cultured mouse chondrocytes ↑ specific gene expression (COX-2), ↑ inflammatory response (PGE2 release), ↓ specific gene expression (collagen II; de-differentiation role)
16C Histamine28, 29, 43 10−32 Mol/L Human basophils ↓ CD203c expression
14C–18C Adrenaline43 10−28–10−36 Mol/L Human basophils ↓ histamine release, ↓ CD 63 and CD203c expression
15C–20C (pooled) Cadmium44 10−30–10−40 Mol/L Human lymphocytes ↑ Resistance to cadmium toxicity
45X Arsenic45, 46 10−45 Mol/L Arsenic-intoxicated wheat seeds ↑ Germination

↓ Gene expression levels
30C Arnica mont.47 Not reported Escherichia coli ↑ Resistance to RX toxicity
30C Arsenicum alb.48 10−60 Mol/L Escherichia coli ↑ Resistance to arsenicum toxicity
30C Carcinosinum22 Not reported DLA cells ↑ specific gene expression (p53 pro-apoptotic)
30C Arsenicum alb.49 10−60 Mol/L Saccharomyces cerevisiae ↑ Resistance to arsenicum toxicity

↓↑ expression of specific genes (apoptotic gene, stress response proteins)
30C Thuja50 Not reported Mouse primary lung cells ↑ Resistance to benzopyrene toxicity, ↓ free radical production

↓ heat shock protein hsp-90 expression
30C Condurango51 Not reported H460-non-small-cell lung cancer (NSCLC) cells ↓↑ expression of specific genes (apoptotic markers), ↑ Apoptosis, oxidative stress, mitochondrial depolarization
100C Sabal serr.52 Not reported PC-3 cancer cells ↓ Proliferation
200C Ruta grav.21 Not reported DLA cells ↑ Apoptosis
200C Mercurius sol.36 10−404 Mol/L Mice peritoneal macrophages ↓ Free radicals production
200C Carcinosinum22 Not reported DLA cells ↑ specific gene expression (p53 pro-apoptotic)
200C Carcinosinum, Hydrastis, Ruta or Thuja23 Not reported DLA cells ↑ Apoptosis, ↓↑ Gene expression (whole genome analysis)
∗All these results were reported as statistically significant. ↑=increase, ↓=decrease, ↑↓=different effects on different genes.
When homeopathic drugs were tested in the same assay system at increasing dilutions, in most cases the greatest effects were observed at the lowest dilutions and also in Mother Tinctures (high molecular concentrations), but the same activity remained even at high dilutions.20, 29, 30, 43 In other cases, the effect was noted only in the low potencies.31 In many instances, when the dilution exceeded the Avogadro constant, the effects appeared as pseudo-sinusoidal curves, with peaks of activity at certain dilutions/dynamizations, followed by inactive or less active dilutions.19, 29, 53, 54, 55, 56 Many of these effects have also been explained mechanistically as modifications of receptors, transduction mechanisms and gene expression changes. As there are many levels of cell regulation, there is no single mechanism explaining homeopathic effects, just as there is no single mechanism explaining the effects of conventional drugs.

High sensitivity to external regulations and nonlinear responses are frequently reported also with non-dynamized dilutions. For example, recent studies measured the responses of mouse fibroblasts to TNF-α in terms of nuclear factor κB (NF-κB) gene expression.57 A fraction of cells in the population can respond to concentrations of TNF-α as low as few pg/ml (10−12 g) and in a nonlinear manner. In fact, early NF-κB gene expression is not dependent on the concentration of the inducing signal. Moreover, the cell response was expressed as dynamical oscillations of NF-κB translocations, whose frequency can produce distinct gene expression profiles.58
It is worth pointing out that not all homeopathic effects can be reduced to the cellular level. A clear example is the recent finding that Calcarea carbonica induced regression of Ehrlich’s ascites carcinoma in mice and 30–35% tumour cell apoptosis in vivo, but failed to induce any significant cell death when administered to cancer cells in vitro.59 This apparent discrepancy was explained considering that Calcarea carbonica employs the immuno-modulatory circuit to assert its antitumour effects. Another example concerns carefully conducted experiments in which rats injected with prostate tumour cell lines developed fewer tumours when also exposed to the homeopathic remedies Conium maculatum 1000C, Sabal serrulata 200C, Thuja occidentalis 1000C, and Carcinosinum 1000C for 5 weeks.60 However, the same drugs did not affect in vitro outcomes like cell viability and apoptosis gene expression, suggesting that in vivo effects are due to other mechanisms – possibly at a more systemic level – which are still to be clarified.

Effects on gene expression
Table 2 documents the ability of highly diluted compounds to modulate gene expression in human/animal cells and unicellular organisms. In experiments conducted in microbiological models (arsenite or UV treated E. coli and Saccharomyces cultures), ultradiluted Arsenicum album 30C or Arnica montana 30C modified the expression of specific genes that are the targets of arsenite and UV irradiation injury, respectively.47, 48, 49 Ultrahigh diluted arsenic (45X treatment, containing a theoretical dose of As2O3 10−47 Mol/L) applied to wheat seedlings, poisoned with a sublethal dose of arsenic, produced a strong gene modulating effect compared to pure water (control).46 Authors have suggested that diluted arsenic treatment induced a reequilibration of those genes that were up-regulated during poisoning. Mother tinctures and highly diluted drugs were tested in human tumour cell lines or cells challenged with carcinogens; they affected the modulation of the expression of specific mRNA markers (NF-κB, Akt, p53, Bax, Blc-2, caspase 3, Cyt-c) and increased tumour cell death.22, 41, 50, 51 These findings support the hypothesis that homeopathic remedies could turn some important genes on or off, initiating a cascade of gene actions to correct the gene expression that has gone wrong and produced the disorder or disease. In this hypothesis the relevant target gene should be sensitive to similar stimuli and exert a pleiotropic transcriptional regulation on a battery of genes with related functions. Needless to say, these in vitro effects are very interesting but cannot support the use of high dilutions in the treatment of cancer. In several studies cited above, not all the cells used, nor all the dilutions tested, gave positive results.

Preethi and coworkers investigated the effects of antitumour homeopathic medicines (Ruta 200C, Carcinosinum 200C, Hydrastis 200C, Thuja 1M and 200C) through the analysis of expression changes in the whole genome using DNA microarray.23 Thuya 1M induced the expression change of a large number of genes (about 600), including genes involved in the process of apoptosis (up-regulated) and genes acting as second messengers in the process of tumorigenesis (down-regulated). The ultradiluted drugs also overexpressed diverse genes (about 100), which had a common role in induction of apoptosis.

Extremely low copper concentrations – from 10−6 Mol/L to 10−17 Mol/L – modified gene expression profiles of a human prostate epithelial cell line.61 Many genes belonging to functional gene families (metallothioneins and heat shock proteins) were modulated by copper in a dose-dependent way, while others were modulated in a dose-independent way, at all concentrations tested.

Our results30, 31 prove the extremely high sensitivity of the human neurocyte gene network to centesimal dilutions (2C, 3C, 4C, 5C, 9 C and 30C) of Gelsemium s. As observed using DNA microarray analysis, Gelsemium s. 2C significantly modulated the expression of 56 genes (49 are down-regulated and 7 up-regulated) involved in neuronal functions (G-protein coupled receptor signalling pathways, calcium homeostasis, inflammatory response and neuropeptide receptors).

The expression of these genes decreased significantly, although with small changes, also after treatment with medium dilution (3C, 4C and 5C) and high dilutions of Gelsemium s. (9C and 30C). In the study conducted using the real-time PCR technique (RT-PCR Array),31 exposure of a human neurocyte cell line to Gelsemium s. 2C dilution, containing a nanomolar concentration of the active principle gelsemine, induced a down-regulation of most genes of this array. In particular, the treated cells showed a statistically significant down-regulation of the prokineticin receptor 2, whose ligand is a neuropeptide involved in nociception, and in depression-like behaviour. In the latter study, the 9C dilution was not active.

The difference between the two gene-expression studies30, 31 was probably due to technical factors: while real-time PCR is the ‘gold standard’ for gene expression analysis of specific genes or small groups of genes, microarray is a powerful screening method for the whole genome and in our conditions exhibited higher sensitivity, detecting extremely low dose effects.

Further experiments conducted on resting epithelial cell lines treated with Apis mellifica MT, 3C, 5C and 7C dilutions20 reported modified expression of hundreds of genes after 24 h incubation (MT: 391 genes up- and 495 down-regulated; 3C: 558 up- and 483 down-regulated; 5C: 132 up- and 168 down-regulated; 7C: 328 up- and 352 down-regulated). The main reduced functions were cytokine expression and inflammatory processes, while anti-oxidative responses and proteasome degradation were up-regulated. Groups of genes were diversely expressed by the MT or by 3C, 5C and 7C dilutions, suggesting a hormetic response. Other groups of genes were modulated only by high dilutions but not by the MT. On the basis of DNA microarray data, it has been suggested that gene regulatory networks may be regarded as dynamically ‘critical’ systems poised near the transition phase between order and chaos,62, 63 where extreme sensitivity to initial conditions and small perturbations are known to occur. Genetic regulatory networks may be the target of subtle messages by virtue of their flexibility in response to environmental stimuli.63
The physical–chemical state of the compounds employed plays a critical role. In fact, bio-active ingredients of medicinal plants (e.g. Chelidonium-chelidonine, Lycopodium-apigenin and coumarins) were nano-encapsulated in biodegradable poly(lactide-co-glycolide) (PLGA) polymers in order to increase their bioavailability and cellular uptake, and to boost their apoptotic effects on cells in vitro, compared with the corresponding free extracts; this hypothesis was supported by the results obtained.64, 65

Also the crude extracts of Phytolacca d., Hydrastis c., Gelsemium s., and Thuya o. were used to synthesize silver nanoparticles from aqueous solution of silver nitrate in ambient conditions; they showed the ability to interact with DNA, bringing about better stability, better drug bioavailability, and conformational changes in the DNA.66, 67 It is plausible that these preparations have greater effects on gene expression than free compounds, and the results presented by the authors support the hypothesis that those effects are due to efficient induction of apoptosis.

There is growing evidence for the presence of nanostructures in homeopathically-made medicines.14, 68, 69, 70, 71, 72 The role of nanoparticles presumably deriving from the containers and their interaction with the starting substance and the solvent during the dynamization process32 may be critical since nanoscale forms are not identical in properties to bulk forms of a given material and nanoscale structure may lower dose requirements for triggering or regulating a given biologic event.73, 74, 75, 76

Cell communication and regulation
In the body system, regulatory molecules bind to cell receptors which recognize chemical signals and respond to them with different actions. Following receptor stimulation, a panoply of transduction pathways are triggered, including G-proteins, phospholipid metabolites, protein kinases, calcium waves, proteolytic events, the formation of new complexes or dissociation of others, etc. The final outcome is the triggering or inhibition of effector mechanisms controlling various cell functions like gene expression, metabolism, secretion, movement, etc. All these steps may be the targets of possible pharmaceutical regulation.

Receptors
Cell receptors are proteins situated in the cell membrane or in the cytosol, like steroid receptors. They have different conformations and affinity with ligands, depending on the function they are conducting. Some of them act rapidly, others have a slower effect: this difference depends on the kind of receptor and how many steps there are in the process to evoke a response. There are several types of receptors, including membrane ligand-gated ion channels, G-protein-coupled receptors (GPCRs), kinase-linked and related receptors, and intracellular receptors controlling gene transcription.

According to the classic ‘key-lock’ model, receptors are specific and their activity is passive. However, a basal state of the receptors shows an activity without a ligand,77 a discovery that changed current thinking about receptor functions and their regulation. In the absence of agonists, the level of basal receptor activity is determined by the equilibrium between the resting state and the active one. This equilibrium can be affected by the presence of specific agonists, inverse agonists, antagonists, and also by stochastic fluctuations or quantal effects based on individual responses.78, 79 An agonist may bind and stimulate the maximum activated state but, on the other hand, the inverse agonist shows affinity for the resting state and it acts by reducing the basal activity even more, thus producing biological effects opposite to those produced by an agonist.

Receptors for signal molecules or for other types of messengers (light, electromagnetic signals, stretching, action potentials) are highly plastic: the cells are capable of increasing (hypersensitivity, priming) or decreasing (desensitization, tolerance, adaptation, down-regulation) the number of receptors according to their needs, and also of regulating their activity by modifying the affinity for the signal molecule.

On occasion, the cells may present more than one receptor for the same molecule, but with different affinities and different intracellular effects. Intense stimulation at receptor levels may cause homologous desensitization but at the same time heterologous priming, i.e. increased response to other agonists (cross-sensitization). To give one example, high salt concentrations applied to the tongue desensitize receptors to salt but increase the sensitivity to low doses of capsaicin.80 Changes of sensitivity are very important because they may involve the blockage of homeodynamics in chronic cases while at the same time prompting individual hypersensitivity to similar exogenous signals (drugs), i.e. acting on the same regulatory system. These new signals, in turn, may unblock the pathologic attractor and re-activate the homeodynamic networks, as previously outlined.15, 17, 81, 82, 83

Regulation and adaptation
Drugs induce an adaptation of the receptor and transduction mechanism that leads either to the loss or to a change in the efficacy of receptor autoregulation. Tolerance decreases the primary pharmacological effect and produces symptoms that are the opposite of the desired physiological situation. An example is GPCRs which stop activating second messenger cascades so that there is a decrease in the number of receptors expressed. This means that receptors are internalized inside the cells and/or that there is a decrease in receptor synthesis. The internalized receptors can be re-cycled and used whenever the cell needs a greater response. For instance, if the ligand is not present in the required quantity, more receptors show up in the cell membrane, in order to capture as much ligand as possible; this reverse phenomenon is known as up-regulation.

Benzodiazepines (BDZs) are generally used in anxiety disorders when the organism suffers a spontaneous down-regulation of GABA(A) receptors, which means that the GABAergic circuit does not work properly. BDZs are GABA(A) receptor allosteric modulators, which enhance the effect of the GABA neurotransmitter that calms down the organism. One of the main problems in clinical use of GABA(A) receptor agonists is the development of tolerance and dependence. The anti-anxiety effect is significant if BDZs are used for a short period of time, otherwise they may cause rebound excitation due to their secondary action.84 Most of these drugs, in long-term use and during withdrawal, have been associated with important modulations of receptor subunit expression in a brain-region-specific manner, participating in the mechanisms of tolerance and dependence.

Another example is morphine, an agonist of the Mu receptor; whenever there is an excessive presence of the ligand, the receptors are down-regulated by a balance mechanism inside the organism, and more pain is perceived.85
Hormones are both natural mediators and drugs which are subject to complex regulations and pleiotropic targets, including inverse effects according to the dose and the dynamics of delivery (e.g. continuous or pulsed-dose). A typical example of this situation is adrenocorticotropic hormone (ACTH), which causes the adrenal secretion of cortisol. This agent is also able to alter splenic lymphocyte activation; a paradoxical dose–response curve resulted when there are low or high level of ACTH. Very low doses (10−12, 10−11 Mol/L) stimulated cell growth whereas higher levels (10−7, 10−6 Mol/L) reversed the effect and are suppressive of lymphocyte growth.86
Pulsed-dose therapy provided by nasal administration of estradiol at the dose of 0.3 mg per day prevents bone loss in postmenopausal women87 and reduces climacteric symptoms and is at least as effective as 2 mg oral estradiol or patch delivery, but with better tolerance.88 In the latter trial, estradiol concentration reached a single peak of approximately 0.000014 mg/ml.

Signal transduction
GPCRs convey the majority of signal transductions across cell membranes. They are activated by diverse ligands, which vary from single photons (in rhodopsin) through ions, odorants, amino acids, fatty acids, neurotransmitters, peptides/polypeptides, to proteolytic enzymes, which cleave off receptor fragments to generate an activating ligand and adhesion molecules. One of the very special features of GPCRs is that they are highly druggable, to the extent that more than one third of all current therapeutic agents are directed at them.89 On the other hand, they are also the target of bacterial toxins, and several oncogenic mutations are associated with these structures.

Intracellular systems couple receptor activation with production of signals or activation of effector mechanisms; they are associated with enzyme activities, variations of intracellular second messengers, modifications of membrane lipids and proteins, and the opening of ion channels. The level of responsiveness is controlled at various levels in the cell and is modified during the course of disease; differential expression and recruitment of these pathways provide a mechanism for subtle physiological regulation of cellular activity.89
Small changes in the concentration and/or oscillation frequency in second messengers like free calcium, protons (H+), cyclic adenosine monophosphate (AMP) and phospholipid derivatives can induce allosteric modifications of enzyme functions, chain-reactions and cascades of intracellular signals, and eventually gene expression. We showed in a leukocyte model that inverse effects of different doses of a bacterial agonist depend on the ‘gating’ exerted by cyclic AMP on the transduction pathways of different agonists.90, 91, 92, 93 Antigen-induced, IgE-mediated release of histamine from human basophils is an in vitro model of allergic reactions; it is blocked by extracellular histamine, presumably as a result of its ability to increase cyclic AMP levels.94 Interestingly, this control is still preserved when histamine is highly diluted.29, 55

Epigenetics
The epigenetic regulation of gene expression could be accounted for as an adaptive response to external stimuli due to the dynamic changes typical of this event. During the critical period of development, epigenetic alterations due to environmental stress permanently alter chromatin structure, thus affecting the function of cells and organs and increasing susceptibility to disease later in life.95 For example in an adverse prenatal environment, like famine, a different pattern of methylation was observed for various genes involved in growth and metabolism,96 associated with increased risk of obesity and cardiovascular disease in maturity.97 However the effects associated with early-life epigenetic modulation could be also beneficial. For example, maternal dietary supplementation during pregnancy with methyl donors, like betaine, choline, folic acid and vitamin B12, is associated with reduction in the risk of developing neural defects, obesity, diabetes and cancer.98 This adaptive epigenetic rearrangement can also serve to buffer the organism against environmental alterations.99
The finely tuned epigenetic modulation prompted by external detrimental events could be seen from a hormetic perspective. For example moderate stress, like modest physical activity and caloric restriction, has been shown to increase body fitness, prevent disease and improve quality of life through activation of antioxidant enzymes and proteins.100 In yeast, transiently elevating mitochondrial oxidative stress, generally considered as pathogenic factors responsible for ageing, mediate a hormetic longevity signal101; this signal epigenetically modulates the chromatin binding capacity of the histone demethylase at subtelomeres, resulting in lifespan extension.

In some cases it has been shown that radiation to a localized area of the body can reduce tumour growth in a site outside that field of radiation.102 This phenomenon (‘abscopal effect’) implies a complex interplay of different regulation pathways prompting a protective response from the whole organism.103 The epi-reprogramming carried out by mildly-stressed bystander cells can prime distant cells for augmented defence against more threatening future insults.104
In this context, we would also mention the studies according to which epigenetic changes may have transgenerational transmission.105 Exposure of a rodent to a non-lethal dose of common-use fungicide modifies the brain chemistry and behavioural response of the subsequent generations to stressors.106 This is an important demonstration in an animal that ancestral exposure to an environmental compound modifies the susceptibility of descendants to a stress challenge experienced during their own life history.

In humans, a correlation of dietary intake of micronutrients in pregnant women and behaviour of offspring has been reported. For example, in a recent study an inverse correlation between maternal intake of iron and the risk of autism spectral disorders was found.107 Early developmental periods are critical and prevention of iron deficiency might be a key for protecting against adverse neurodevelopmental outcomes. In context of epigenetics and the developmental origins of adult disease, it is noteworthy that exposure to dietary isoflavones during foetal development reduces the susceptibility to cardiovascular diseases and obesity in adulthood.108
Together, these findings suggest that an environmental event in one generation could affect the phenotype in subsequent generations, and these somewhat Lamarckian ideas are stimulating new interest in biology, ecology, and medicine.

Since evidence of gene expression changes induced by homeopathic drugs is accumulating, it is conceivable that some action is mediated by epigenetic modifications of related genes. However, direct proof of this possible molecular mechanism of drug action is still lacking. In our recent studies Gelsemium s. 2C treatment of SHSY5Y neurocytes reduced the expression of several genes30, 31 but did not induce marked general epigenetic changes. The only significant finding was an increased methylation (53% compared to 28% for the controls) of the homeobox A1 gene, which has a role in neural development and autism spectrum disorders (Olioso et al., unpublished results).

Sensitization and response to stress
Cells can respond to damage and stress by activating various repair and survival pathways. Low, sublethal doses of the same stresses provoke a prosurvival response, based on a number of molecular modifications.109 These changes include Sirtuin-1, Histone deacetylase, AMP activated protein kinase, the Forkhead family of transcription factors, Nuclear factor-2 transcription factor, heat-shock proteins, DNA repair genes, antioxidant enzyme induction, receptor up-regulation, and proteasome activity. Also Bcl-2, an anti-apoptotic protein recognized by its antioxidant and prosurvival functions, has been shown to play an important role during oxidative-conditioning hormesis.110 Suboptimal function of these mechanisms can lead to disease, while their stimulation by a ‘small’ heterologous stress may be one of the molecular mechanisms explaining post-conditioning hormesis at cell level.12, 111, 112 A more general model for the action of homeopathic remedies based on stimulation of the organism’s biological stress response network has been proposed by Bell and coworkers.113 This model is based on the idea that the resilience and recovery from disease is due to time-dependent sensitization of host responses which reverse pathology direction.

In modern terms, the concept of ‘susceptibility’ due to both genetic and environmental factors can be compared with the original concept of ‘miasm’, as an idea of chronic disorders which make humans vulnerable to diseases. Although the concept of miasm is questionable by scientific pathology,114, 115 Hahnemann seemed to equate miasms to the different ways in which humans can be susceptible to various diseases; as scabies and venereal diseases were widespread in the 19th century, considering them – and their suppression with inappropriate medication of that time – as the source of vulnerabilities for other maladies is obvious.116 Hahnemann also pioneered the concept of disease prevention when he stated that continuous exposure to noxious environmental influences undermines health (Organon, par. 77). In the same paragraph it is explicit that if a person can avoid noxious influences, he/she would lead a healthier life. The previous paragraph also mentions ‘constant state of worry’ as a noxious influence, showing Hahnemann as a forerunner also in the recognition of stress as a predisposing factor to illness.

The inversion of effects
Inverse and paradoxical effects of drugs constitute outcomes which are the opposite of those that would be expected from the drug’s known actions. In medical history, Hahnemann was the first to consider a primary and a secondary action of medicines, the latter being the opposite of the former. In the Organon (par. 63–67), he mentioned three examples, the actions of wine, coffee and opium: “The man who yesterday was warmed by too much wine (primary action) today feels chilly from every little draft (counteraction of the organism, secondary action). […] Excessive liveliness results from taking strong coffee (primary action), but afterward lethargy and drowsiness remain for a long time (counteraction, secondary action) unless removed by the repeated taking of more coffee (brief palliations). The heavy, stuporous sleep of opium (primary action) is followed on the next night by greater insomnia (counteraction, secondary action). […] Thus, to the primary action of every substance that in large doses strongly alters the condition of a healthy body our vital force always produces in the secondary action the exactly opposite condition (when, as stated above, such a condition exists).”117
Modern pharmacology has recognized how such reactions arise in a wide variety of drug classes. Some are common; others have been noted in single case reports.118 There are many possible mechanisms explaining the inverse effects of drugs, one of which is hormesis, with beneficial or stimulatory effects at low doses and adverse or inhibitory effects at high doses. Hormesis was originally applied in toxicology and radiation toxicity, but its importance is also obvious in pharmacology, since most drugs are essentially xenobiotics. Enhanced antioxidant defences, microsomal detoxification, clearance, augmented DNA repair, synthesis of heat shock proteins, or other compensatory responses have been offered as explanations.109 The hormesis framework has been extended to include the influence of pre- or post-exposure conditioning and the similarity principle at the cell level.12, 17, 92, 111, 112, 119, 120

In homeopathy, a number of highly toxic substances are used in low doses or high dilutions as therapeutic agents. Two major examples supported by scientific literature and basic research are phosphorus33, 121, 122, 123, 124, 125, 126 and arsenic.48, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139 Interestingly, the paradoxical anticancer power of the carcinogen arsenic was noted also by non-homeopathic literature.140 Research data strongly suggest that arsenic influences distinct signalling pathways involved in mediating proliferation or apoptosis, according to different doses and target systems.

But hormesis is insufficient to explain the paradoxical effects of non-toxic substances such as antibodies or hormones. Moreover, the hormetic paradigm is still inadequate to include opposite responses in healthy and sick patients, which is the foundation of homeopathic treatment. Inverse effects of non-toxic molecules can be the consequence of secondary adaptations of cell receptors, which normally occur in numerous daily situations, such as after physical exercise, drinking coffee or taking a BDZ.

Caffeine is a stimulant due to its competitive antagonism of adenosine receptors, preventing the adenosine from acting as an inhibitor of the central nervous system. When there is chronic consumption, adenosine receptors are up-regulated141, 142 and the effect presents as headache, fatigue and apathy. The differential effects of caffeine in low and high users was demonstrated using functional magnetic resonance imaging, and showed up-regulation of adenosine receptors in high users, resulting in differential contributions of the neural and vascular effects of adenosine in the two study populations.143
In the marathon run, physical activity is linked to an increase of catecholamine levels, which is also associated with stress. Catecholamines are captured by alpha and beta adrenoceptors in order to activate the sympathetic nervous system. In the chronic exposure to these endogenous ligands (noradrenaline and adrenaline) found in trained runners, the concentration of plasma catecholamines in blood rises but receptor levels in blood cells decrease. Therefore, the surplus of catecholamines produces a down-regulation of the adrenoceptors.144 The consequence of down-regulation of adrenoceptors is linked to a specific behaviour: the decrease in noradrenergic activity, in addition to endorphine production, causes the pleasant sensation deriving from physical effort and reduces pathologic reactions to stress.

Paradoxical pharmacology
Chronic heart failure (CHF) is pathophysiologically characterized by adrenergic overactivity resulting from the failure of cardiac pump function, leading to decreased blood pressure and tissue perfusion. Impaired beta adrenergic receptor signalling and function is a hallmark underlying mechanism of CHF145; use of β-agonists was found to give no benefit and to increase mortality.146 But the paradoxical employment of β blockers (BBs) substantially decreased mortality in comparison with placebo and beta agonists.147 Long-term BBs therapy is associated with an increase in myocardial beta-receptor density, significant improvement in resting haemodynamic output, and improved contractile response to catecholamine stimulation.148
The benefit noted in the treatment of CHF begs the question whether a similar paradoxical approach can be constructed for asthma, where the current therapy is still based on beta-agonists.149 The therapeutic power of inverse effects is also exploited in the treatment of diabetes insipidus, where thiazides have long provided paradoxical antidiuretic benefit.150 The importance of this emerging field is highlighted by a commentary paper in Trends in Pharmacological Sciences entitled “Paradoxical pharmacology: turning our pharmacological models upside down”.151
Some paradoxical and bidirectional adverse effects are common and well known, e.g. agitation during paediatric sedation with midazolam, dysrhythmias from antidysrhythmic drugs, hyperalgesia from opioids, bradycardia with low-dose atropine, early suicidality with antidepressants, pulmonary oedema with diuretics.118
The basis of paradoxical pharmacology was clearly expressed by Bond147: “Can exacerbating a disease make use of the body’s compensatory and redundant mechanisms to achieve a beneficial long-term response? Can we use drugs that, according to traditional views, would be considered to increase stress on the system in the short term, to actually treat and cure disease in the long term? Is it possible to exacerbate disease for a longer-term gain? (…) Where to begin? If acute versus chronic responses are often opposite in nature, and if the contraindications have been made based on the acute effects, there is a suggested list where basic research can begin to look for clues to investigate paradoxical pharmacology. It is the list under ‘Contraindications’ because the opposite of contraindicated is indicated. A short-term discomfort may produce longer-term benefit.” Similar concepts were expressed by Yun et al152: “The modern medical paradigm based on blocking overactive pathways or augmenting deficient pathways offers symptomatic benefit, but tolerance to therapy can develop and treatment cessation can produce rebound symptoms due to compensatory mechanisms. We propose a paradoxical strategy for treating chronic conditions based on harnessing compensatory mechanisms for therapeutic benefit. The therapeutic effect is derived from compensatory response, rather than drug effect. (…) The concept may generalize to many other diseases, especially those involving pathways which exhibit strong homeostatic tendencies such as the neurologic, immune, and endocrine systems.”

On the basis of these scientific facts, the logic of homeopathic reasoning is evident: if the body regulates itself in the opposite direction to the stimulus, we can use this property, giving low, sub-toxic, doses of pathogenic substances that trigger a counter-regulation. That this strategy is extremely close to the Hahnemannian concept of primary and secondary reactions to drugs has also been noted by others.153 While the absorption and distribution of a drug (pharmacokinetics) is quite universal in a species, varying in a narrow range, the response to drugs (pharmakodynamics) is individualized, because it depends on multiple factors which, in turn, depend on the genetic and epigenetic characteristics of individuals, along with the current conditions at the time of treatment. At a particular dose (fixed or weight-based) in a population, a xenobiotic may produce anticipated effects with a range of effect magnitudes, including people who respond as expected, but also non-responders, excessive or toxic effects, and inverse effects. The proportion producing a paradoxical effect and the shape of the distribution differ for each xenobiotic and population.118 Clearly, the homeopathic approach is individualized and no single drug can be used in all the persons affected by the same disease, a principle which is quite coherent with modern concepts of pharmacogenomics.

The Simile at molecular level: allosteric regulation
The specificity of any drug effect is based on the interaction of active principles with their biological targets (cells and molecules), and the same is conceivably true for homeopathic drugs.15 At a molecular level, pharmacology recognizes the classic distinction between allosteric drugs and orthosteric drugs. Orthosteric drugs bind to the active site of a target enzyme or a receptor and block it; allosteric drugs bind elsewhere on the protein and indirectly alter the conformations at the active site (see Figure 1). Orthosteric drugs shut off native protein function; allosteric drugs modulate it.154
Thumbnail image of Figure 1. Opens large image
Figure 1
Allosteric and orthosteric drug actions. Allosteric (A) and orthosteric (O) regulation of different macromolecules. A: Enzymes; B: Cell receptors; D: Membrane channels and transport mechanisms; E: Gene expression at the promoter site.

In the following sections we show how homeopathic drugs may work by exploiting the characteristic features of allosteric regulation. The fundamental issues of homeopathic drug action, sensitivity, specificity, nonlinearity and opposite effects depending on the context, are all rooted in the very behaviour of proteins and nucleic acids, the most important and informative molecular moieties of life.

Basic concepts of allostery
Allostery is a universal phenomenon in the chemistry of life, which in traditional terms may be regarded as the essential, tiniest, dynamic factor of the ‘vital force’. The term comes from the Greek allos (ἄλλoς), ‘other’, and stereos (στɛρɛὀς), ‘solid (object)’, in reference to the fact that the regulatory site of an allosteric protein is physically distinct from its active site. In fact, allosteric regulation is exerted by a factor acting at a protein’s allosteric site, that is a site other than the active site where the function or the reaction mediated by the protein takes place. Effectors that enhance the protein’s activity are referred to as allosteric activators, whereas those that decrease the protein’s activity are called allosteric inhibitors.155
Long-range allostery is especially important in cell signalling and also in disease, where all co-occurring allosteric events (including posttranslational modifications, pathogen binding, and mutations) collectively tag the protein functional sites and regulate events like cell activation, proliferation and/or death.156 Allosteric perturbation is common in cell physiology: it arises from noncovalent events, such as binding of ions, lipids, cyclicAMP, drugs, proteins, RNA, or DNA; from light absorption and from covalent events, such as phosphorylation, point mutations, or reaction with a small molecule. Allostery takes place in all dynamic protein single chains, in multimolecular assemblies and in RNA and DNA polymers.157

Figure 1.  Allosteric and orthosteric drug actions. Allosteric (A) and orthosteric (O) regulation of different macromolecules. A: Enzymes; B: Cell receptors; D: Membrane channels and transport mechanisms; E: Gene expression at the promoter site.
Figure 1.
Allosteric and orthosteric drug actions. Allosteric (A) and orthosteric (O) regulation of different macromolecules. A: Enzymes; B: Cell receptors; D: Membrane channels and transport mechanisms; E: Gene expression at the promoter site.

Figure 1 shows four examples of allosteric and orthosteric drug regulation of important biochemical and signalling cell functions, namely enzymes, receptors, ionic channels, and gene expression. All the current models hold that binding at the allosteric site regulates the activity (increasing or decreasing it) without blocking it, while orthosteric binding at the active site blocks the function of the protein in question. For example, the enzyme cyclooxygenase-2 is orthosterically blocked by aspirin but is allosterically regulated by non substrate fatty acids.

The activity of membrane-bound enzymes is controlled by the lipidic milieu in which they are embedded, as in the case of free-radical generation by nicotine adenine dinucleotide phosphate (NADPH) oxidase.158 Interestingly, transition metal ions such as copper and zinc, which are crucial in many physiological and pathophysiological pathways,159 also act as versatile allosteric modulators at low doses.160 Allosteric signals transmit through multiple, pre-existing pathways; which pathways dominate depends on protein topologies, specific binding events, covalent modifications, and cellular (environmental) conditions. Consequently the observed functional, conformational, and dynamic effects will be different.161
The same principle also operates in pharmacology. Allosteric drugs present several key advantages over orthosteric drugs that target a protein’s functional site.157 They are highly specific because they do not bind in active sites, which tend to be highly conserved in protein families, and allow modulation of the protein activity rather than completely blocking it. Moreover, allosteric signals may propagate either within a protein, or across several proteins, to enhance or inhibit specific interactions along a pathway and specific cellular functions.162 Allosteric drugs can activate a target protein not only by directly binding, but by modulating the interaction with another (activating or inhibiting) factor, and thereby create a mechanism of tissue-specific fine-tuning.163
Remarkably, the control of protein function and DNA gene expression is exerted not only by endogenous or exogenous specific molecules but also by low frequency electromagnetic fields,164 ion resonance phenomena,165 and water clusters.166, 167, 168, 169, 170 Water molecules do not just play a part in solvation, but also function as chaperone catalysts participating in the regulation of chemical changes in living cells. A ‘water-regulated cycle’ consisting of this type of intracellular network of weak noncovalent connections may be presumed to exist in living cells.15, 171

The protein energy landscape
Proteins are dynamic and flexible polymeric molecules with many degrees of conformational freedom; their final shape and function at a given time is determined by internal energetic interactions and by environmental conditions.172 This can be clarified by the basic physical fact that biomacromolecules consist of ensembles of conformations with a certain distribution, which can be described by their free-energy landscape.154
As shown in Figure 2, if we plot the different possible conformations of a protein along the horizontal axis and the free energy along the vertical axis, we obtain what can be described as an energy state–space plot, or energy landscape. This is a representation of all the possible states of a protein, where higher-energy states (far from equilibrium) are unstable and have the tendency to descend towards more stable states, where free energy is lower. This map encompasses the native conformation as well as any nonnative conformations, which may form during folding or interaction with other molecules.157 In living beings, the optimal utilization of energy is the main aim of the ‘vital force’ and is accomplished by biologic information, at genetic, epigenetic and systemic network levels.

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Figure 2
Graphic summary of how allostery works. Allostery is considered from the thermodynamic standpoint, in terms of the energy landscape of population shift. A: A simplified folding funnel of the state-space or energy landscape of a protein that occupies distinct energy minima; B: Allosteric two-state model presenting a balance between the inactive state (left) and the active state (right) binding to an allosteric ligand; C: detachment of the ligand destabilizes the protein energy and the population balance shifts to the left.

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The free energy landscape theory has transformed the field of protein folding.173 According to this perspective, in the low-dimensional representations, because of the induced entropic contribution to the full free energy, the whole plot of the attraction basin appears funnel-like.154 Depending on structural constraints and external conditions (temperature, chemical concentrations, pH and so on), a protein may belong to different sub-spaces, which lead it to naturally settle on different conformations.

Proteins with their different possible conformations ‘explore’ the energy landscape by searching the sub-spaces to find a narrow energetic alley that contains the protein’s most favourable configurations. These sub-spaces have to be considered as ‘attractors’ in the energy landscape and represent the spontaneous emergence of ordered states from a variety of possible states; in this position, single molecules or molecular complexes have greater stability because they are situated in a local minimum within their energy state-space.

In the most simple picture, the protein can be viewed as populating one of two states: active or inactive (see Figure 2B–C). The basins of the two states are separated by a surmountable barrier, which allows the conformations to switch between the states. The model holds that, in the absence of any ligand (substrate or otherwise), equilibrium favours one of the conformational states. The presence of allosteric regulators ‘perturbs’ the free energy of the protein and changes its state-space landscape, stabilizing or de-stabilizing specific sub-spaces. In this way, the populations of active/inactive proteins distribute themselves in diverse attractors and the functional configuration of a given protein shifts to up- or down-regulated states. The population balance can be shifted to the active state (or vice-versa) through the noncovalent binding of one ligand or other minimal alterations at the allosteric site. When the protein is found near or at the top of an energetic barrier, its unstable position can be regarded as a bifurcation point of its trajectory in the space-state, where a minimal energy and informational influences – such as those exerted by highly diluted/dynamized compounds – could operate the ‘switch’ between active and inactive states.

Since allosteric sites are less conserved in evolution than orthosteric sites, they are subject to greater polymorphism in the population; consequently, the response to drugs becomes more flexible and individual. It depends on genetic predisposition (heredity), epigenetics (pathobiologic history, concomitant diseases, nutrition) and the context in which the drug is taken (receptor affinity, synergy, priming, desensitization).

Dynamics in health and disease
In Figure 3 the sequential changes of a model protein are represented in the space-states populated by the different conformations. The ‘healthy’ state of a protein – and of a cell – is normally characterized by a ‘resting state’ that minimizes energy loss and allows the protein to adapt and respond to perturbations (3A). Of course, if the protein is a functional repressor or inhibitor, its functional activity is normally ‘ON’, in the interest of the whole economy of the cell’s energy expenditure.

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Figure 3
Changes of the protein energy landscape in normal (A–C) and pathologic (D–F) conditions. A: Resting state, where the basal activity and energy of the target protein system is low; B: The allosteric regulator enhances the activity in a normal, regulated way; C: Return to basal state after inactivation or detachment of the ligand; D: A pathogenic factor binds to the same protein and triggers a dysregulated activity, in a reversible way since the energy barrier is low and unsound (hallmark of acute diseases); E: The pathogenic factor markedly alters the structure of the protein in a way that is not spontaneously reversible (chronic disease); F: The protein is trapped in a minimum energy trough and can’t return to normal shape even if the pathologic factor is no longer bound (self-maintained chronic disease).

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Panel 3B shows the new state-space of the protein during interaction with an allosteric stimulator: if the protein is an enzyme, the result is a product; if we are considering a receptor, a specific signal transduction cascade is triggered, leading to some function. After completion of the required activity, the stimulus ceases, the stimulant is removed and the system spontaneously returns to the basal attractor (3C). This may occur through a variety of mechanisms such as inactivation of the ligand (e.g. acetylcholine in synaptic transmission), dilution and diffusion of the ligand (e.g. cytokines in inflammatory exudate), feed-back inhibition by the physiologic products of a reaction (e.g. most metabolic enzymes), or auto-phosphorylation of the receptor itself (e.g. epidermal-growth factor receptor). Despite the importance of this essential step, further analysis is outside the scope of this review.

The bottom panels of Figure 3 illustrate a conceptual model of the situation during pathology. Needless to say, diseases may have thousands of different causes and mechanisms and this is a schematic and oversimplified representation of one single, albeit essential, notion of general pathology. A perturbation of free energy is caused by a factor that binds to the protein, activating it in some anomalous, undesired way.

This pathologic factor may be exogenous (like bacterial toxins, pollution, viruses, radiation, etc.) or endogenous (like complement components, tumour-necrosis factor, oxygen free radicals, excess of hormones, etc.). The perturbation may be transitory or permanent, as in the case of genetic mutations. For example, aminoacid sequence mutations or binding of toxins can redistribute the ensemble to favour the ON state, making the protein constitutively active.157 The resulting anomalous activity is translated to irregular functions and, directly or indirectly through a chain of further alterations, to disease symptoms and structural harm.

Many oncogenic mutations of growth factor receptors or of protein kinases exemplify the latter case. Similarly, binding of virus proteins, neurotoxins, as well as the sun and UV irradiation, may all interfere with signalling via (often subtle) changes in the relative stabilities of conformational states in populations of proteins. For example, disruption of glucocorticoid steroid signalling plays a role in diverse disease states, including depression, leukaemia, and asthma.157, 174

Schematically, pathologic modifications are represented by two different situations: acute (Panel D) and chronic (E and F). Acute variations are characterized by high energy consumption, marked symptoms, short duration and often by self-limitation. Spontaneous healing in acute cases is due both to the reaction itself, which is capable of eliminating (or killing) the pathogen, and to the small and easily removed energy barrier dividing the pathologic attractor from the normal one. Thus, when the pathogen is removed, the protein population exploring the space of states can easily recover the normal, physiologic, resting state.

In chronic pathology we have two possibilities, one in which the pathologic factor is strongly bound to the protein and is currently present (Figure 3, panel E); for example, in tuberculosis the mycobacteria are always present during disease, and the same is true for human immunodeficiency virus (HIV) infection, etc. In this category we can also include hereditary or acquired mutations of genetic information, which represent a permanent variation of the primary aminoacid sequence and therefore a strong constraint for the secondary structure and folding conformation.

In other instances, the pathologic factor gives rise to a disorder of protein dynamics that places the system in an attractor characterized by a stable self-organization separated from the healthy state (panel F). Therefore, even if the originating factor is no longer present, the system is unable by itself to find the way to re-enter the normal attractor basin. Examples are autoimmune and rheumatic diseases, originating from an infection and perpetuated by an internal disorder of the immune system which maintains the pathology even after elimination of the invading microorganism.

Allosteric dynamics and the ‘Simile’
Recently, Nussinov et al.154 addressed the question of how very similar ligands can bind at the same allosteric site, with one acting as an agonist and the other as antagonist. The chemical difference between allosteric agonists and antagonists – which bind at the same site – can be surprisingly small: even a change of a single atom or a small group may result in opposite outcomes or in substantial differences in efficacy. The slight structural changes between the conformations involve residues and hydrogen bonds that are responsible for the dynamic oscillations between states. A small change in the allosteric site increases the probability of a corresponding large change at the functional site, pushing the inactive conformation into the active state, or vice-versa. Further, even the same allosteric ligand bound at the same site can lead to opposite effects in different environments175: Tamoxifen has oestrogen antagonist activity in breast tissue but shows oestrogen-like activity in other tissues.

Figure 4 illustrates the hypothesis of allosteric action of the ‘Simile’ in acute diseases: the same substance that is capable of interaction with the allosteric site and of stimulating the protein in a normal situation is also capable of binding to the same protein in the pathologic state. The resulting composite shifts the configuration of the protein far from the natural pathologic attractor towards a new position (panel B), from which the situation of normal activation state is easily reached (panel C), partly because the reaction itself contributes to the elimination of the initial cause. Then, ‘physiologic’ stimulation is regulated as in a normal situation and this kind of stimulation is reversible to the resting, basal, state (Panel D).

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Figure 4
Protein energy landscape in pathologic conditions (acute case) and ‘therapeutic’ action of allosteric regulation. A: The protein system is pathologically activated; B: The allosteric factor destabilizes the protein and starts regulation; C: The pathologic factor is removed and the protein is normally activated; D: Spontaneous return to normal, healthy, state.

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In chronic disease (Figure 5), the dynamics of healing catalysed by the allosteric ‘Simile’ follow a sequence in which the drug first shifts the protein far from pathologic adaptation and lowers the energy barrier (panel B), after which the protein population gradually recovers a new configuration typical of physiologic activation (panel C), from which it spontaneously reaches the resting state when the influence of the allosteric drug ceases (panel D). In this case, too, the homeopathic principle lies in the similarity between the ‘normal’ configurations induced by the remedy in the healthy state (see Figure 3B) and the ‘dysregulated’ configurations typical of the unhealthy state (Figure 5A) which need to be treated. The remedy based on the similarity principle acts in the diseased state as an ‘artificial’ perturbation which is ‘stronger’ than the current pathologic configuration. The therapeutic action is stronger because its capacity to bind and affect its specific protein target has evolved by evolution as a natural way to recover the resting, energetically favourable, state.

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Figure 5
Protein energy landscape in chronic pathologic conditions and ‘therapeutic’ action of allosteric regulation. A: The protein system is chronically activated and dysregulated; B: The allosteric factor destabilizes the protein and reduces the energy barrier to a normal level (possible increase of activity); C: The pathologic conformation is no longer involved and the protein becomes activated in a normal way; D: Spontaneous return to normal, healthy, state.

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There is some preliminary indication that homeopathic remedies may act through allosteric regulation of receptors. An example is Gelsemium s., whose anxiolytic-like activity in rat neurons is inhibited by strychnine, a convulsant alkaloid, which acts as an allosteric inhibitor of the glycine receptor.34, 176 Homeopathic dilutions of Ignatia a., whose major active principle is strychnine, have a small but statistically significant anxiolytic-like activity in laboratory mice.177

Symptom similarity at molecular level
A summary of the similia principle applied at the molecular level is shown in Figure 6. Since an active protein is linked to an active function, and the latter is expressed by ‘symptoms’, it is reasonable to conceive the ‘simile’ as an allosteric regulation of the same protein system in health (‘Proving’) and in disease (in this case represented by a pathologic attractor of the same protein). In connection with this illustration of the traditional ‘Simile’, we note that the protein target of allosteric regulation in pathology is the same as that considered in the healthy system above; therefore, since the activation of a protein produces specific ‘symptoms’ due to the perturbation of the related function, the ‘symptoms’ caused by this pathology (Figure 6, panel D) are ‘similar’ to those caused by activation in a normal state (Figure 6, panel B). The difference lies in the fact that during pathology those symptoms are manifested in a dysregulated way, for example they are too strong and painful, have longer duration and/or are present in anomalous sites in the body. Since in ‘real’ diseases a number of different proteins and functions are affected, and since all protein perturbations and consequent reactions are determined by the individual genetic constitution, each sick person presents a complex pattern of different symptoms.

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Figure 6
Summary of the similarity principle (‘similia similibus curentur’) based on allosteric stimulation of a functional protein system. A: Normal ‘healthy’ state; B: Stimulation and appearance of a pattern of symptoms, specific and typical of the molecular system(s) involved (‘proving’); C: return to basal state; D: Chronic disease situation of the same molecular system(s), whose inappropriate activity produces a pattern of similar symptoms; E: Intervention of the ‘Simile’ signal which interacts with the same molecular system and starts normal regulation; F: Spontaneous self organization in the normal, physiologic attractor of the activated state, similar to ‘B’; G: Spontaneous return to basal state (‘healing’).

This conceptual illustration of the ‘simile’ at molecular level is consistent with the traditional Hahnemannian view according to which drugs have two different effects: the primary and the secondary actions. The primary action is the actual effect of the drug on the healthy organism. The secondary action is the spontaneous and opposite action of the organism in the presence of an external substance, the drug, in order to restore a balance in the organism itself.

This is also connected with the use of very small doses of drugs in homeopathy. The effect of low and ultra-low doses is possible where the target systems, as a consequence of pathologic influences, are situated in far from equilibrium and unstable states in the energy landscape. It is tempting to speculate that the power of homeopathic treatment is the employment of high dilution medicines in order to lessen the primary action, the one similar to the disease, leaving active the secondary healing reaction. The latter effect depends not so much on the dose as on the sensitivity of the target system, which needs specific information about the complex pattern of various alterations of the whole person.

This view of the similarity principle confirms the theoretical advantage of homeopathy, embracing the principle of the secondary action of medicine to cure a disease. The homeopathic drug, acting on a sick organism in critically sensitive conditions, can move the system components – at molecular, cellular and systemic levels – away from energetically unfavourable pathological attractors, readdressing them toward more physiological ones.

Perspectives
Despite the preliminary and oversimplified nature of this model, the allosteric action of homeopathic drugs prompts interesting perspectives and working hypotheses:

a.Allostery works by preferential interaction of a signal with one state over the other (in simple terms, ON versus OFF), accompanied by a shift of the ensemble toward this state (Figure 2B,C). Since the interaction signal-allosteric site is influenced by minimal differences in either the allosteric ligand or the receptor protein, this delicate conformational equilibrium may underpin pathology (e.g. excess basal activity of an enzyme) but also therapeutics based on the ‘simile’. This scheme can be verified for homeopathic drugs by analysing their physicochemical state before and after dynamization. In fact, it is highly conceivable that dynamization, that involves high shearing forces, nanobubbles, oxygen free radicals, water clusters, etc.178 may induce small but significant changes in the physicochemical nature of the active principles.
b.The effect of homeopathic allosteric intervention may also be accomplished by an indirect influence on the target protein system. For example, in the classic hormetic models, resistance and healing is due (also) to the synthesis of heat shock proteins, whose role is to refold the native proteins whose secondary structure has been damaged by toxic xenobiotics. In ‘sick’ cells, the synthesis of those proteins may be insufficient or suboptimal, and the low dose may act epigenetically on the promoter of the same or similar heat shock proteins, thus increasing resistance. This hypothesis is fully in keeping with the results of the long series of studies from the laboratory of Wiegant and Van Wijk.12, 179
c.The scheme of Figure 5, Figure 6 also makes it possible to understand why using the ‘simile’ sometimes (but not always) may cause an apparent worsening of symptoms, when stimulation by the drug may be superimposed on the activity of the pathogenic factors. A change of attractor (in this case from pathologic to physiologic) requires the overcoming of an energy barrier, and this may require an increase of energy expenditure for a certain time, until the new attractor basin is reached.180 However, the barrier dividing the two attractors may be very small and even small, subtle changes can make a difference.
d.In homeopathy, drugs are composed of natural substances which are never ‘pure’, i.e. they contain a number of different compounds. This means that allosteric regulations simultaneously have multiple targets, adding a noteworthy level of complexity and of pleiotropicity to the therapeutic intervention.
e.Signal transduction pathways and gene regulatory circuits underpin integrated cellular responses to perturbations, characterized by a number of mechanisms that amplify small percentage changes in the input signal into larger percentage changes in the output response. Ultrasensitivity is a form of nonlinear signal processing whereby a small fractional change in the input signal is amplified, producing a larger fractional change in the output response.181 Common types of ultrasensitive regulation in intracellular molecular networks are positive cooperative binding, protein multimerization, multistep signalling, positive feedback and stochastic resonance.15 The importance for homeopathy of this kind of signal amplification – typical of biological networks characterized by nonlinear dynamics, adaptation and oscillation at the edge of chaos – has previously been suggested by us180, 182 and by others.16
f.The classic homeopathic method of drug discovery was originally based on careful observation of symptoms because at that time there was no knowledge of the ‘intimate nature’ of disease processes and of pharmacodynamic actions. The conceptual model presented here helps us to understand that the two perspectives – ‘holistic’, based on symptoms of the whole person and ‘reductionistic’, based on cellular and molecular changes – are not in contrast but have the same heuristic connotation. With the introduction of modern ‘omics’ techniques, the knowledge basis of homeopathic drug actions on healthy and sick people can be deepened to the molecular level.
These prospects, by increasing the credibility and plausibility of homeopathic concepts, allow us to include this pharmacological approach in the mainstream of modern science. However, plausibility is by no means certain proof, so research in this area still has a long way to go. It is important that homeopathic drugs, in different doses and formulations, be tested for pathways such as heat shock response, protein folding/unfolding, epigenetic mechanisms, gene expression and so on. Existing laboratory evidence of homeopathic drugs should be better linked with models of receptor function, cell regulation, and human findings (from both provings and clinical trials), in a system biology framework. How these concepts fit into homeopathy is important and requires further development.

Acknowledgements
Experimental work was supported by grants from Boiron Laboratoires to Verona University – Department of Pathology and Diagnostics and from Italian Research Ministry. The authors have no conflicts of interest.

The original article is here: http://www.sciencedirect.com/science/article/pii/S1475491615000053

References
Weatherall, M.W. Making medicine scientific: empiricism, rationality, and quackery in mid-Victorian Britain. Soc Hist Med. 1996; 9: 175–194
View in Article | CrossRef | PubMed
Giles, J. Degrees in homeopathy slated as unscientific. Nature. 2007; 446: 352–353
View in Article | CrossRef | PubMed | Scopus (7)
Shang, A., Huwiler-Müntener, K., Nartey, L., Jüni, P., Dörig, S., Sterne, J.A.C. et al. Are the clinical effects of homoeopathy placebo effects? Comparative study of placebo-controlled trials of homoeopathy and allopathy. Lancet. 2005; 366: 726–732
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (406)
Kleijnen, J., Knipschild, P., and ter Riet, G. Clinical trials of homoeopathy. BMJ. 1991; 302: 316–323
View in Article | CrossRef | PubMed
Dillon, L.R. Homeopathy? Absurd [letter; comment]. Am J Health Syst Pharm. 1996; 53: 1339
View in Article | PubMed
Gold, P.W., Novella, S., Roy, R., Marcus, D., Bell, I., Davidovitch, N. et al. Homeopathy–quackery or a key to the future of medicine?. Homeopathy. 2008; 97: 28–33
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (7)
Rutten, L., Mathie, R.T., Fisher, P., Goossens, M., and Van Wassenhoven, M. Plausibility and evidence: the case of homeopathy. Med Health Care Philos. 2013; 16: 525–532
View in Article | CrossRef | PubMed | Scopus (4)
de Oliveira, C.C., de Oliveira, S.M., Goes, V.M., Probst, C.M., Krieger, M.A., and Buchi, D.F. Gene expression profiling of macrophages following mice treatment with an immunomodulator medication. J Cell Biochem. 2008; 104: 1364–1377
View in Article | CrossRef | PubMed | Scopus (17)
Burbano, R.R., Leal, M.F., da Costa, J.B., Bahia, M.O., de Lima, P.D., Khayat, A.S. et al. Lymphocyte proliferation stimulated by activated human macrophages treated with Canova. Homeopathy. 2009; 98: 45–48
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (8)
Iavicoli, I., Calabrese, E.J., and Nascarella, M.A. Exposure to nanoparticles and hormesis. Dose Response. 2010; 8: 501–517
View in Article | CrossRef | PubMed | Scopus (27)
Rattan, S.I. and Deva, T. Testing the hormetic nature of homeopathic interventions through stress response pathways. Hum Exp Toxicol. 2010; 29: 551–554
View in Article | CrossRef | PubMed | Scopus (5)
Van Wijk, R. and Wiegant, F.A. Postconditioning hormesis and the similia principle. Front Biosci (Elite Ed). 2011; 3: 1128–1138
View in Article | PubMed
Demirovic, D. and Rattan, S.I. Establishing cellular stress response profiles as biomarkers of homeodynamics, health and hormesis. Exp Gerontol. 2013; 48: 94–98
View in Article | CrossRef | PubMed | Scopus (19)
Bell, I.R. and Schwartz, G.E. Adaptive network nanomedicine: an integrated model for homeopathic medicine. Front Biosci (Schol Ed). 2013; 5: 685–708
View in Article | CrossRef | PubMed
Bellavite, P., Marzotto, M., Olioso, D., Moratti, E., and Conforti, A. High-dilution effects revisited. 2. Pharmacodynamic mechanisms. Homeopathy. 2014; 103: 22–43
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (3)
Bell, I.R., Baldwin, C.M., and Schwartz, G.E. Translating a nonlinear systems theory model for homeopathy into empirical tests. Altern Ther Health Med. 2002; 8: 58–66
View in Article | PubMed
Bellavite, P. and Signorini, A. The emerging science of homeopathy: complexity, biodynamics, and nanopharmacology. Berkeley (CA), North Atlantic; 2002
View in Article
Ghosh, S., Bishayee, K., Paul, A., Mukherjee, A., Sikdar, S., Chakraborty, D. et al. Homeopathic mother tincture of Phytolacca decandra induces apoptosis in skin melanoma cells by activating caspase-mediated signaling via reactive oxygen species elevation. J Integr Med. 2013; 11: 116–124
View in Article | CrossRef | PubMed | Scopus (11)
Arora, S., Aggarwal, A., Singla, P., Jyoti, S., and Tandon, S. Anti-proliferative effects of homeopathic medicines on human kidney, colon and breast cancer cells. Homeopathy. 2013; 102: 274–282
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (2)
Bigagli, E., Luceri, C., Bernardini, S., Dei, A., Filippini, A., and Dolara, P. Exploring the effects of homeopathic Apis mellifica preparations on human gene expression profiles. Homeopathy. 2014; 103: 127–132
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (1)
Preethi, K.C., Kuttan, G., and Kuttan, R. Anti-tumour activity of Ruta graveolens extract. Asian Pac J Cancer Prev. 2006; 7: 439–443
View in Article | PubMed
Sunila, E.S., Kuttan, R., Preethi, K.C., and Kuttan, G. Dynamized preparations in cell culture. Evid Based Complement Altern Med. 2009; 6: 257–263
View in Article | CrossRef | PubMed | Scopus (11)
Preethi, K., Ellanghiyil, S., Kuttan, G., and Kuttan, R. Induction of apoptosis of tumor cells by some potentiated homeopathic drugs: implications on mechanism of action. Integr Cancer Ther. 2012; 11: 172–182
View in Article | CrossRef | PubMed | Scopus (3)
Chirumbolo, S., Conforti, A., Lussignoli, S., Metelmann, H., and Bellavite, P. Effects of Podophyllum peltatum compounds in various preparations dilutions on human neutrophil functions in vitro. Br Hom J. 1997; 86: 16–26
View in Article | Abstract | Full Text PDF
Hostanska, K., Rostock, M., Melzer, J., Baumgartner, S., and Saller, R. A homeopathic remedy from arnica, marigold, St. John inverted question marks wort and comfrey accelerates in vitro wound scratch closure of NIH 3T3 fibroblasts. BMC Complement Altern Med. 2012; 12: 100
View in Article | CrossRef | PubMed | Scopus (4)
Manduca, P., Marchisio, S., Astigiano, S., Zanotti, S., Galmozzi, F., Palermo, C. et al. FMS*Calciumfluor specifically increases mRNA levels and induces signaling via MAPK 42,44 and not FAK in differentiating rat osteoblasts. Cell Biol Int. 2005; 29: 629–637
View in Article | CrossRef | PubMed | Scopus (8)
Palermo, C., Filanti, C., Poggi, S., and Manduca, P. Osteogenesis in vitro in rat tibia-derived osteoblasts is promoted by the homeopathic preparation, FMS*Calciumfluor. Cell Biol Int. 1999; 23: 31–40
View in Article | CrossRef | PubMed | Scopus (4)
Sainte-Laudy, J. and Belon, P. Improvement of flow cytometric analysis of basophil activation inhibition by high histamine dilutions. A novel basophil specific marker: CD 203c. Homeopathy. 2006; 95: 3–8
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (13)
Chirumbolo, S., Brizzi, M., Ortolani, R., Vella, A., and Bellavite, P. Inhibition of CD203c membrane up-regulation in human basophils by high dilutions of histamine: a controlled replication study. Inflamm Res. 2009; 58: 755–764
View in Article | CrossRef | PubMed | Scopus (27)
Marzotto, M., Olioso, D., Brizzi, M., Tononi, P., Cristofoletti, M., and Bellavite, P. Extreme sensitivity of gene expression in human SH-SY5Y neurocytes to ultra-low doses of Gelsemium sempervirens. BMC Complement Altern Med. 2014; 14: 104
View in Article | CrossRef | PubMed | Scopus (3)
Olioso, D., Marzotto, M., Moratti, E., Brizzi, M., and Bellavite, P. Effects of Gelsemium sempervirens L. on pathway-focused gene expression profiling in neuronal cells. J Ethnopharmacol. 2014; 153: 535–539
View in Article | CrossRef | PubMed | Scopus (2)
Bhattacharyya, S.S., Mandal, S.K., Biswas, R., Paul, S., Pathak, S., Boujedaini, N. et al. In vitro studies demonstrate anticancer activity of an alkaloid of the plant Gelsemium sempervirens. Exp Biol Med (Maywood ). 2008; 233: 1591–1601
View in Article | CrossRef | PubMed | Scopus (32)
Chirumbolo, S., Signorini, A., Bianchi, I., Lippi, G., and Bellavite, P. Effects of homeopathic preparations of organic acids and of minerals on the oxidative metabolism of human neutrophils. Br Hom J. 1993; 82: 227–244
View in Article | Abstract | Full Text PDF | Scopus (5)
Venard, C., Boujedaini, N., Mensah-Nyagan, A.G., and Patte-Mensah, C. Comparative analysis of gelsemine and Gelsemium sempervirens activity on neurosteroid allopregnanolone formation in the spinal cord and limbic system. Evid Based Complement Altern Med. 2011; 2011: 407617
View in Article | CrossRef | PubMed | Scopus (3)
Samadder, A., Das, S., Das, J., Paul, A., Boujedaini, N., and Khuda-Bukhsh, A.R. The potentized homeopathic drug, Lycopodium clavatum (5C and 15C) has anti-cancer effect on hela cells in vitro. J Acupunct Meridian Stud. 2013; 6: 180–187
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (2)
de Oliveira, S.M., de Oliveira, C.C., Abud, A.P., Guimaraes, F.S., Di Bernardi, R.P., Coletto, E.L. et al. Mercurius solubilis: actions on macrophages. Homeopathy. 2011; 100: 228–236
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (5)
Pathak, S., Multani, A.S., Banerji, P., and Banerji, P. Ruta 6 selectively induces cell death in brain cancer cells but proliferation in normal peripheral blood lymphocytes: a novel treatment for human brain cancer. Int J Oncol. 2003; 23: 975–982
View in Article | PubMed
Baumgartner, S., Thurneysen, A., and Heusser, P. Growth stimulation of dwarf peas (Pisum sativum L.) through homeopathic potencies of plant growth substances. Forsch Komplementarmed Klass Naturheilkd. 2004; 11: 281–292
View in Article | CrossRef | PubMed | Scopus (17)
de Oliveira, C.C., Abud, A.P., de Oliveira, S.M., Guimaraes, F.S., de Andrade, L.F., Di Bernardi, R.P. et al. Developments on drug discovery and on new therapeutics: highly diluted tinctures act as biological response modifiers. BMC Complement Altern Med. 2011; 11: 101
View in Article | CrossRef | PubMed | Scopus (4)
Guedes, J.R., Carrasco, S., Ferreira, C.M., Bonamin, L.V., Souza, W., Goldenstein-Schainberg, C. et al. Ultra high dilution of triiodothyronine modifies cellular apoptosis in Rana catesbeiana tadpole tail in vitro. Homeopathy. 2011; 100: 220–227
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (6)
Hofbauer, R., Pasching, E., Moser, D., and Frass, M. Heparin-binding epidermal growth factor expression in KATO-III cells after Helicobacter pylori stimulation under the influence of strychnos Nux vomica and Calendula officinalis. Homeopathy. 2010; 99: 177–182
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (1)
Huh, Y.H., Kim, M.J., and Yeo, M.G. Homeopathic Rhus toxicodendron treatment increased the expression of cyclooxygenase-2 in primary cultured mouse chondrocytes. Homeopathy. 2013; 102: 248–253
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (1)
Mannaioni, P.F., Mastroianni, R., and Mastrangelo, D. Adrenaline inhibits the immunological activation of human basophils at pharmacological and ultra-low doses. Med Sci Monit. 2010; 16: BR227–BR232
View in Article | PubMed
Walchli, C., Baumgartner, S., and Bastide, M. Effect of low doses and high homeopathic potencies in normal and cancerous human lymphocytes: an in vitro isopathic study. J Altern Complement Med. 2006; 12: 421–427
View in Article | CrossRef | PubMed | Scopus (9)
Brizzi, M., Lazzarato, L., Nani, D., Borghini, F., Peruzzi, M., and Betti, L. A biostatistical insight into the As2O3 high dilution effects on the rate and variability of wheat seedling growth. Forsch Komplementarmed Klass Naturheilkd. 2005; 12: 277–283
View in Article | CrossRef | PubMed | Scopus (19)
Marotti, I., Betti, L., Bregola, V., Bosi, S., Trebbi, G., Borghini, G. et al. Transcriptome profiling of wheat seedling following treatment with ultrahigh diluted arsenic trioxide. Evid Based Complement Altern Med. 2014; 2014: 851263
View in Article | CrossRef | PubMed
Das, S., Saha, S.K., De, A., Das, D., and Khuda-Bukhsh, A.R. Potential of the homeopathic remedy, Arnica Montana 30C, to reduce DNA damage in Escherichia coli exposed to ultraviolet irradiation through up-regulation of nucleotide excision repair genes. Zhong Xi Yi Jie He Xue Bao. 2012; 10: 337–346
View in Article | CrossRef | PubMed
De, A., Das, D., Dutta, S., Chakraborty, D., Boujedaini, N., and Khuda-Bukhsh, A.R. Potentiated homeopathic drug Arsenicum Album 30C inhibits intracellular reactive oxygen species generation and up-regulates expression of arsenic resistance gene in arsenite-exposed bacteria Escherichia coli. Zhong Xi Yi Jie He Xue Bao. 2012; 10: 210–227
View in Article | CrossRef | PubMed | Scopus (7)
Das, D., De, A., Dutta, S., Biswas, R., Boujedaini, N., and Khuda-Bukhsh, A.R. Potentized homeopathic drug Arsenicum Album 30C positively modulates protein biomarkers and gene expressions in Saccharomyces cerevisae exposed to arsenate. Zhong Xi Yi Jie He Xue Bao. 2011; 9: 752–760
View in Article | CrossRef | PubMed | Scopus (9)
Mukherjee, A., Boujedaini, N., and Khuda-Bukhsh, A.R. Homeopathic Thuja 30C ameliorates benzo(a)pyrene-induced DNA damage, stress and viability of perfused lung cells of mice in vitro. J Integr Med. 2013; 11: 397–404
View in Article | CrossRef | PubMed
Sikdar, S., Mukherjee, A., Ghosh, S., and Khuda-Bukhsh, A.R. Condurango glycoside-rich components stimulate DNA damage-induced cell cycle arrest and ROS-mediated caspase-3 dependent apoptosis through inhibition of cell-proliferation in lung cancer, in vitro and in vivo. Environ Toxicol Pharmacol. 2014; 37: 300–314
View in Article | CrossRef | PubMed | Scopus (2)
MacLaughlin, B.W., Gutsmuths, B., Pretner, E., Jonas, W.B., Ives, J., Kulawardane, D.V. et al. Effects of homeopathic preparations on human prostate cancer growth in cellular and animal models. Integr Cancer Ther. 2006; 5: 362–372
View in Article | CrossRef | PubMed | Scopus (17)
Davenas, E., Beauvais, F., Amara, J., Robinson, M., Miadonna, A., Tedeschi, A. et al. Human basophil degranulation triggered by very dilute antiserum against IgE. Nature. 1988; 333: 816–818
View in Article | CrossRef | PubMed
Poitevin, B., Davenas, E., and Benveniste, J. In vitro immunological degranulation of human basophils is modulated by lung histamine and Apis mellifica. Br J Clin Pharmacol. 1988; 25: 439–444
View in Article | CrossRef | PubMed
Belon, P., Cumps, J., Ennis, M., Mannaioni, P., Roberfroid, M., Sainte-Laudy, J. et al. Histamine dilutions modulate basophil activation. Inflamm Res. 2004; 53: 181–188
View in Article | CrossRef | PubMed | Scopus (95)
Endler, P., Thieves, K., Reich, C., Matthiessen, P., Bonamin, L., Scherr, C. et al. Repetitions of fundamental research models for homeopathically prepared dilutions beyond 10(-23): a bibliometric study. Homeopathy. 2010; 99: 25–36
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (32)
Tay, S., Hughey, J.J., Lee, T.K., Lipniacki, T., Quake, S.R., and Covert, M.W. Single-cell NF-kappaB dynamics reveal digital activation and analogue information processing. Nature. 2010; 466: 267–271
View in Article | CrossRef | PubMed | Scopus (220)
Ashall, L., Horton, C.A., Nelson, D.E., Paszek, P., Harper, C.V., Sillitoe, K. et al. Pulsatile stimulation determines timing and specificity of NF-kappaB-dependent transcription. Science. 2009; 324: 242–246
View in Article | CrossRef | PubMed | Scopus (215)
Saha, S., Hossain, D.M., Mukherjee, S., Mohanty, S., Mazumdar, M., Mukherjee, S. et al. Calcarea carbonica induces apoptosis in cancer cells in p53-dependent manner via an immuno-modulatory circuit. BMC Complement Altern Med. 2013; 13: 230
View in Article | CrossRef | PubMed | Scopus (2)
Jonas, W.B., Gaddipati, J.P., Rajeshkumar, N.V., Sharma, A., Thangapazham, R.L., Warren, J. et al. Can homeopathic treatment slow prostate cancer growth?. Integr Cancer Ther. 2006; 5: 343–349
View in Article | CrossRef | PubMed | Scopus (15)
Bigagli, E., Luceri, C., Bernardini, S., Dei, A., and Dolara, P. Extremely low copper concentrations affect gene expression profiles of human prostate epithelial cell lines. Chem Biol Interact. 2010; 188: 214–219
View in Article | CrossRef | PubMed | Scopus (5)
Ramo, P., Kesseli, J., and Yli-Harja, O. Perturbation avalanches and criticality in gene regulatory networks. J Theor Biol. 2006; 242: 164–170
View in Article | CrossRef | PubMed | Scopus (47)
Balleza, E., varez-Buylla, E.R., Chaos, A., Kauffman, S., Shmulevich, I., and Aldana, M. Critical dynamics in genetic regulatory networks: examples from four kingdoms. PLoS ONE. 2008; 3: e2456
View in Article | CrossRef | PubMed | Scopus (50)
Paul, A., Das, S., Das, J., Samadder, A., and Khuda-Bukhsh, A.R. Cytotoxicity and apoptotic signalling cascade induced by chelidonine-loaded PLGA nanoparticles in HepG2 cells in vitro and bioavailability of nano-chelidonine in mice in vivo. Toxicol Lett. 2013; 222: 10–22
View in Article | CrossRef | PubMed | Scopus (6)
Das, S., Das, J., Samadder, A., Paul, A., and Khuda-Bukhsh, A.R. Strategic formulation of apigenin-loaded PLGA nanoparticles for intracellular trafficking, DNA targeting and improved therapeutic effects in skin melanoma in vitro. Toxicol Lett. 2013; 223: 124–138
View in Article | CrossRef | PubMed | Scopus (4)
Bhattacharyya, S.S., Paul, S., Dutta, S., Boujedaini, N., and Khuda-Bukhsh, A.R. Anti-oncogenic potentials of a plant coumarin (7-hydroxy-6-methoxy coumarin) against 7,12-dimethylbenz [a] anthracene-induced skin papilloma in mice: the possible role of several key signal proteins. Zhong Xi Yi Jie He Xue Bao. 2010; 8: 645–654
View in Article | CrossRef | PubMed | Scopus (17)
Das, S., Das, J., Samadder, A., Bhattacharyya, S.S., Das, D., and Khuda-Bukhsh, A.R. Biosynthesized silver nanoparticles by ethanolic extracts of Phytolacca decandra, Gelsemium sempervirens, Hydrastis canadensis and Thuja occidentalis induce differential cytotoxicity through G2/M arrest in A375 cells. Colloids Surf B Biointerfaces. 2013; 101: 325–336
View in Article | CrossRef | PubMed | Scopus (21)
Rao, M.L., Roy, R., Bell, I.R., and Hoover, R. The defining role of structure (including epitaxy) in the plausibility of homeopathy. Homeopathy. 2007; 96: 175–182
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (53)
Chikramane, P.S., Suresh, A.K., Bellare, J.R., and Kane, S.G. Extreme homeopathic dilutions retain starting materials: a nanoparticulate perspective. Homeopathy. 2010; 99: 231–242
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (41)
Czerlinski, G. and Ypma, T. Homeopathic potentization based on nanoscale domains. J Altern Complement Med. 2011; 17: 1165–1173
View in Article | CrossRef | PubMed | Scopus (2)
Upadhyay, R.P. and Nayak, C. Homeopathy emerging as nano medicine. Int J High Dilution Res. 2011; 10: 299–310
View in Article
Chikramane, P.S., Kalita, D., Suresh, A.K., Kane, S.G., and Bellare, J.R. Why extreme dilutions reach non-zero asymptotes: a nanoparticulate hypothesis based on froth flotation. Langmuir. 2012; 28: 15864–15875
View in Article | CrossRef | PubMed | Scopus (12)
Bhattacharyya, S.S., Paul, S., and Khuda-Bukhsh, A.R. Encapsulated plant extract (Gelsemium sempervirens) poly (lactide-co-glycolide) nanoparticles enhance cellular uptake and increase bioactivity in vitro. Exp Biol Med (Maywood). 2010; 235: 678–688
View in Article | CrossRef | PubMed | Scopus (24)
Bhattacharyya, S.S., Das, J., Das, S., Samadder, A., Das, D., De, A. et al. Rapid green synthesis of silver nanoparticles from silver nitrate by a homeopathic mother tincture Phytolacca decandra. Zhong Xi Yi Jie He Xue Bao. 2012; 10: 546–554
View in Article | CrossRef | PubMed | Scopus (8)
Sarkar, S., Zhang, L., Subramaniam, P., Lee, K.B., Garfunkel, E., Strickland, P.A. et al. Variability in bioreactivity linked to changes in size and zeta potential of diesel exhaust particles in human immune cells. PLoS ONE. 2014; 9: e97304
View in Article | CrossRef | PubMed
Dayem, A.A., Kim, B., Gurunathan, S., Choi, H.Y., Yang, G., Saha, S.K. et al. Biologically synthesized silver nanoparticles induce neuronal differentiation of SH-SY5Y cells via modulation of reactive oxygen species, phosphatases, and kinase signaling pathways. Biotechnol J. 2014; 9: 934–943
View in Article | CrossRef | PubMed | Scopus (2)
de Ligt, R.A., Kourounakis, A.P., and IJzerman, A.P. Inverse agonism at G protein-coupled receptors: (patho)physiological relevance and implications for drug discovery. Br J Pharmacol. 2000; 130: 1–12
View in Article | CrossRef | PubMed
Lutz, W.K., Lutz, R.W., and Andersen, M.E. Dose-incidence relationships derived from superposition of distributions of individual susceptibility on mechanism-based dose responses for biological effects. Toxicol Sci. 2006; 90: 33–38
View in Article | CrossRef | PubMed | Scopus (4)
Rothman, J.S. and Silver, R.A. Data-driven modeling of synaptic transmission and integration. Prog Mol Biol Transl Sci. 2014; 123: 305–350
View in Article | CrossRef | PubMed
Dessirier, J.M., O’Mahony, M., Iodi-Carstens, M., Yao, E., and Carstens, E. Oral irritation by sodium chloride: sensitization, self-desensitization, and cross-sensitization to capsaicin. Physiol Behav. 2001; 72: 317–324
View in Article | CrossRef | PubMed | Scopus (13)
Bellavite, P., Lussignoli, S., Semizzi, M., Ortolani, R., and Signorini, A. The similia principle. From cellular models to regulation of homeostasis. Br Hom J. 1997; 86: 73–85
View in Article | Abstract | Full Text PDF
Signorini, A., Andrioli, G., Ortolani, R., Conforti, A., and Bellavite, P. The similia principle revisited. Theoretical bases and experimental evidence for a physio-pathological model based on the reactivation of homeostatic communication. Homeopath Links. 2001; 13: 227–233
View in Article
Bellavite, P., Ortolani, R., Pontarollo, F., Pitari, G., and Conforti, A. Immunology and homeopathy. 5. The rationale of the ‘simile’. Evid Based Complement Altern Med. 2007; 4: 149–163
View in Article | CrossRef | PubMed | Scopus (35)
Uusi-Oukari, M. and Korpi, E.R. Regulation of GABA(A) receptor subunit expression by pharmacological agents. Pharmacol Rev. 2010; 62: 97–135
View in Article | CrossRef | PubMed | Scopus (67)
Martini, L. and Whistler, J.L. The role of mu opioid receptor desensitization and endocytosis in morphine tolerance and dependence. Curr Opin Neurobiol. 2007; 17: 556–564
View in Article | CrossRef | PubMed | Scopus (101)
Wermerskirchen, A.S., LaTocha, D.H., and Clarke, B.L. Adrenocorticotropic hormone controls Concanavalin A activation of rat lymphocytes by modulating IL-2 production. Life Sci. 2000; 67: 2177–2187
View in Article | CrossRef | PubMed | Scopus (21)
Nielsen, T.F., Ravn, P., Bagger, Y.Z., Warming, L., and Christiansen, C. Pulsed estrogen therapy in prevention of postmenopausal osteoporosis. A 2-year randomized, double blind, placebo-controlled study. Osteoporos Int. 2004; 15: 168–174
View in Article | CrossRef | PubMed | Scopus (27)
Devissaguet, J.P., Brion, N., Lhote, O., and Deloffre, P. Pulsed estrogen therapy: pharmacokinetics of intranasal 17-beta-estradiol (S21400) in postmenopausal women and comparison with oral and transdermal formulations. Eur J Drug Metab Pharmacokinet. 1999; 24: 265–271
View in Article | CrossRef | PubMed
Millar, R.P. and Newton, C.L. The year in G protein-coupled receptor research. Mol Endocrinol. 2010; 24: 261–274
View in Article | CrossRef | PubMed | Scopus (69)
Bellavite, P., Chirumbolo, S., Lippi, G., Andrioli, G., Bonazzi, L., and Ferro, I. Dual effects of formylpeptides on the adhesion of endotoxin-primed human neutrophils. Cell Biochem Funct. 1993; 11: 231–239
View in Article | CrossRef | PubMed | Scopus (11)
Carletto, A., Biasi, D., Bambara, L.M., Caramaschi, P., Bonazzi, M.L., Lussignoli, S. et al. Studies of skin-window exudate human neutrophils: increased resistance to pentoxifylline of the respiratory burst in primed cells. Inflammation. 1997; 21: 191–203
View in Article | CrossRef | PubMed | Scopus (8)
Bellavite, P., Chirumbolo, S., Santonastaso, C., Biasi, D., Lussignoli, S., and Andrioli, G. Dose-dependence of the various functional responses of neutrophils to formylpeptides. Activation, regulation, and inverse effects according to the agonist dose and cell condition. in: M. Bastide (Ed.) Signals and Images. Kluwer Acad. Publ., Dordrecht; 1997: 111–119
View in Article | CrossRef
Bellavite, P., Andrioli, G., Lussignoli, S., Signorini, A., Ortolani, R., and Conforti, A. Scientific reappraisal of the “Principle of Similarity”. Med Hypotheses. 1997; 49: 203–212
View in Article | Abstract | Full Text PDF | PubMed | Scopus (16)
Lichtenstein, L.M. and Gillespie, E. The effects of the H1 and H2 antihistamines on “allergic” histamine release and its inhibition by histamine. J Pharmacol Exp Ther. 1975; 192: 441–450
View in Article | PubMed
Bateson, P., Barker, D., Clutton-Brock, T., Deb, D., D’Udine, B., Foley, R.A. et al. Developmental plasticity and human health. Nature. 2004; 430: 419–421
View in Article | CrossRef | PubMed | Scopus (709)
Tobi, E.W., Lumey, L.H., Talens, R.P., Kremer, D., Putter, H., Stein, A.D. et al. DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific. Hum Mol Genet. 2009; 18: 4046–4053
View in Article | CrossRef | PubMed | Scopus (342)
Heijmans, B.T., Tobi, E.W., Lumey, L.H., and Slagboom, P.E. The epigenome: archive of the prenatal environment. Epigenetics. 2009; 4: 526–531
View in Article | CrossRef | PubMed | Scopus (89)
Wolff, G.L., Kodell, R.L., Moore, S.R., and Cooney, C.A. Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice. FASEB J. 1998; 12: 949–957
View in Article | PubMed
Szyf, M. The early life environment and the epigenome. Biochim Biophys Acta. 2009; 1790: 878–885
View in Article | CrossRef | PubMed | Scopus (105)
Ji, L.L., Dickman, J.R., Kang, C., and Koenig, R. Exercise-induced hormesis may help healthy aging. Dose Response. 2010; 8: 73–79
View in Article | CrossRef | PubMed | Scopus (10)
Schroeder, E.A., Raimundo, N., and Shadel, G.S. Epigenetic silencing mediates mitochondria stress-induced longevity. Cell Metab. 2013; 17: 954–964
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (30)
Formenti, S.C. and Demaria, S. Systemic effects of local radiotherapy. Lancet Oncol. 2009; 10: 718–726
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (128)
Vaiserman, A.M. Hormesis and epigenetics: is there a link?. Ageing Res Rev. 2011; 10: 413–421
View in Article | PubMed
Scott, B.R., Belinsky, S.A., Leng, S., Lin, Y., Wilder, J.A., and Damiani, L.A. Radiation-stimulated epigenetic reprogramming of adaptive-response genes in the lung: an evolutionary gift for mounting adaptive protection against lung cancer. Dose Response. 2009; 7: 104–131
View in Article | CrossRef | PubMed | Scopus (3)
Daxinger, L. and Whitelaw, E. Transgenerational epigenetic inheritance: more questions than answers. Genome Res. 2010; 20: 1623–1628
View in Article | CrossRef | PubMed | Scopus (82)
Crews, D., Gillette, R., Scarpino, S.V., Manikkam, M., Savenkova, M.I., and Skinner, M.K. Epigenetic transgenerational inheritance of altered stress responses. Proc Natl Acad Sci U S A. 2012; 109: 9143–9148
View in Article | CrossRef | PubMed | Scopus (84)
Schmidt, R.J., Tancredi, D.J., Krakowiak, P., Hansen, R.L., and Ozonoff, S. Maternal intake of supplemental iron and risk of autism spectrum disorder. Am J Epidemiol. 2014; 180: 890–900
View in Article | CrossRef | PubMed
Siow, R.C. and Mann, G.E. Dietary isoflavones and vascular protection: activation of cellular antioxidant defenses by SERMs or hormesis?. Mol Asp Med. 2010; 31: 468–477
View in Article | CrossRef | PubMed | Scopus (56)
Calabrese, E.J., Bachmann, K.A., Bailer, A.J., Bolger, P.M., Borak, J., Cai, L. et al. Biological stress response terminology: integrating the concepts of adaptive response and preconditioning stress within a hormetic dose-response framework. Toxicol Appl Pharmacol. 2007; 222: 122–128
View in Article | CrossRef | PubMed | Scopus (220)
Luna-Lopez, A., Gonzalez-Puertos, V.Y., Romero-Ontiveros, J., Ventura-Gallegos, J.L., Zentella, A., Gomez-Quiroz, L.E. et al. A noncanonical NF-kappaB pathway through the p50 subunit regulates Bcl-2 overexpression during an oxidative-conditioning hormesis response. Free Radic Biol Med. 2013; 63: 41–50
View in Article | CrossRef | PubMed | Scopus (7)
Wiegant, F.A., Prins, H.A., and Van, W.R. Postconditioning hormesis put in perspective: an overview of experimental and clinical studies. Dose Response. 2011; 9: 209–224
View in Article | CrossRef | PubMed | Scopus (13)
Van Wijk, R. and Wiegant, F.A. Postconditioning hormesis and the homeopathic Similia principle: molecular aspects. Hum Exp Toxicol. 2010; 29: 561–565
View in Article | CrossRef | PubMed | Scopus (15)
Bell, I.R. and Koithan, M. A model for homeopathic remedy effects: low dose nanoparticles, allostatic cross-adaptation, and time-dependent sensitization in a complex adaptive system. BMC Complement Altern Med. 2012; 12: 191
View in Article | CrossRef | PubMed | Scopus (13)
Bellavite, P. and Pettigrew, A. Miasms and modern pathology. Homeopathy. 2004; 93: 65–66
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (4)
Mathur, M. The concept of miasm–evolution and present day perspective. Homeopathy. 2009; 98: 177–180
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (3)
Gulati, R. The concept of miasm. Homeopathy. 2010; 99: 150
View in Article | Abstract | Full Text | Full Text PDF | PubMed
Hahnemann, C.F.S. in: Joseph Reves (Ed.) Organon of Medicine. 5th and 6th edn. Homeopress Ltd (ed. 1994), Haifa; 1842
View in Article
Smith, S.W., Hauben, M., and Aronson, J.K. Paradoxical and bidirectional drug effects. Drug Saf. 2012; 35: 173–189
View in Article | PubMed
Chirumbolo, S., Marzotto, M., Conforti, A., Vella, A., Ortolani, R., and Bellavite, P. Bimodal action of the flavonoid quercetin on basophil function: an investigation of the putative biochemical targets. Clin Mol Allergy. 2010; 8: 13
View in Article | CrossRef | PubMed | Scopus (18)
Wiegant, F. and Van Wijk, R. The similia principle: results obtained in a cellular model system. Homeopathy. 2010; 99: 3–14
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (16)
Bildet, J., Guere, J.M., Saurel, J., Aubin, M., Demerque, D., and Quilichini, R. E’tude de l’action de differentes diluitions de Phosphorus sur l’hepatite toxique du rat. Ann Homéop Fr. 1975; 4: 425–432
View in Article
Palmerini, C.A., Codini, M., Floridi, A., Mattoli, P., Buffetti, S., and Di Leginio, E. The use of Phosphorus 30 CH in the experimental treatment of hepatic fibrosis in rats. in: C. Bornoroni (Ed.) Omeomed92. Editrice Compositori, Bologna; 1993: 219–226
View in Article
Rajkumar, R., Srivastava, S.K., Yadav, M.C., Varshney, V.P., Varshney, J.P., and Kumar, H. Effect of a Homeopathic complex on oestrus induction and hormonal profile in anoestrus cows. Homeopathy. 2006; 95: 131–135
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (11)
de Almeida, L.R., Campos, M.C., Herrera, H.M., Bonamin, L.V., and da Fonseca, A.H. Effects of homeopathy in mice experimentally infected with Trypanosoma cruzi. Homeopathy. 2008; 97: 65–69
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (15)
Mishra, N., Muraleedharan, K.C., Paranjpe, A.S., Munta, D.K., Singh, H., and Nayak, C. An exploratory study on scientific investigations in homeopathy using medical analyzer. J Altern Complement Med. 2011; 17: 705–710
View in Article | CrossRef | PubMed | Scopus (14)
Frass, M., Zagorchev, P., Yurukova, V., Wulkersdorfer, B., Thieves, K., Zedtwitz-Liebenstein, K. et al. Two cases of fulminant hepatic failure from Amanita phalloides poisoning treated additively by homeopathy. Ochsner J. 2014; 14: 252–258
View in Article | PubMed
Betti, L., Brizzi, M., Nani, D., and Peruzzi, M. Effect of high dilutions of Arsenicum album on wheat seedlings from seed poisoned with the same substance. Br Hom J. 1997; 86: 86–89
View in Article | Abstract | Full Text PDF
Cazin, J.C., Cazin, M., Gaborit, J.L., Chaoui, A., Boiron, J., Belon, P. et al. A study of the effect of decimal and centesimal dilutions of arsenic on the retention and mobilisation of Arsenic in the rat. Hum Toxicol. 1987; 6: 315–320
View in Article | CrossRef | PubMed
Brizzi, M., Nani, D., Peruzzi, M., and Betti, L. Statistical analysis of the effect of high dilutions of arsenic in a large dataset from a wheat germination model. Br Hom J. 2000; 89: 63–67
View in Article | Abstract | Full Text PDF | PubMed
Kundu, S.N., Mitra, K., and Bukhsh, A.R. Efficacy of a potentized homoeopathic drug (Arsenicum-album-30) in reducing cytotoxic effects produced by arsenic trioxide in mice: III. Enzymatic changes and recovery of tissue damage in liver. Complement Ther Med. 2000; 8: 76–81
View in Article | Abstract | Full Text PDF | PubMed | Scopus (21)
Kundu, S.N., Mitra, K., and Khuda Bukhsh, A.R. Efficacy of a potentized homeopathic drug (Arsenicum-Aalbum-30) in reducing cytotoxic effects produced by arsenic trioxide in mice: IV. Pathological changes, protein profiles, and content of DNA and RNA. Complement Ther Med. 2000; 8: 157–165
View in Article | Abstract | Full Text PDF | PubMed | Scopus (21)
Datta, S., Mallick, P., and Bukhsh, A.R. Efficacy of a potentized homoeopathic drug (Arsenicum Album-30) in reducing genotoxic effects produced by arsenic trioxide in mice: comparative studies of pre-, post- and combined pre- and post-oral administration and comparative efficacy of two microdoses. Complement Ther Med. 1999; 7: 62–75
View in Article | Abstract | Full Text PDF | PubMed | Scopus (20)
Mitra, K., Kundu, S.N., and Khuda Bukhsh, A.R. Efficacy of a potentized homoeopathic drug (Arsenicum Album-30) in reducing toxic effects produced by arsenic trioxide in mice: II. On alterations in body weight, tissue weight and total protein. Complement Ther Med. 1999; 7: 24–34
View in Article | Abstract | Full Text PDF | PubMed | Scopus (21)
Datta, S., Mallick, P., and Bukhsh, A.R. Efficacy of a potentized homoeopathic drug (Arsenicum Album-30) in reducing genotoxic effects produced by arsenic trioxide in mice: II. Comparative efficacy of an antibiotic, actinomycin D alone and in combination with either of two microdoses. Complement Ther Med. 1999; 7: 156–163
View in Article | Abstract | Full Text PDF | PubMed | Scopus (19)
Belon, P., Banerjee, P., Choudhury, S.C., Banerjee, A., Biswas, S.J., Karmakar, S.R. et al. Can administration of potentized homeopathic remedy, Arsenicum album, alter antinuclear antibody (ANA) titer in people living in high-risk arsenic contaminated areas? I. A correlation with certain hematological parameters. Evid Based Complement Altern Med. 2006; 3: 99–107
View in Article | CrossRef | PubMed | Scopus (17)
Banerjee, P., Biswas, S.J., Belon, P., and Khuda-Bukhsh, A.R. A potentized homeopathic drug, Arsenicum Album 200, can ameliorate genotoxicity induced by repeated injections of arsenic trioxide in mice. J Vet Med A Physiol Pathol Clin Med. 2007; 54: 370–376
View in Article | CrossRef | PubMed | Scopus (17)
Belon, P., Banerjee, A., Karmakar, S.R., Biswas, S.J., Choudhury, S.C., Banerjee, P. et al. Homeopathic remedy for arsenic toxicity? Evidence-based findings from a randomized placebo-controlled double blind human trial. Sci Total Environ. 2007; 384: 141–150
View in Article | CrossRef | PubMed | Scopus (10)
Kokornaczyk, M.O., Trebbi, G., Dinelli, G., Marotti, I., Bregola, V., Nani, D. et al. Droplet evaporation method as a new potential approach for highlighting the effectiveness of ultra high dilutions. Complement Ther Med. 2014; 22: 333–340
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (1)
Khuda-Bukhsh, A.R., Banerjee, A., Biswas, S.J., Karmakar, S.R., Banerjee, P., Pathak, S. et al. An initial report on the efficacy of a millesimal potency Arsenicum Album LM 0/3 in ameliorating arsenic toxicity in humans living in a high-risk arsenic village. Zhong Xi Yi Jie He Xue Bao. 2011; 9: 596–604
View in Article | CrossRef | PubMed
Bode, A.M. and Dong, Z. The paradox of arsenic: molecular mechanisms of cell transformation and chemotherapeutic effects. Crit Rev Oncol Hematol. 2002; 42: 5–24
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (169)
Varani, K., Portaluppi, F., Gessi, S., Merighi, S., Vincenzi, F., Cattabriga, E. et al. Caffeine intake induces an alteration in human neutrophil A2A adenosine receptors. Cell Mol Life Sci. 2005; 62: 2350–2358
View in Article | CrossRef | PubMed | Scopus (13)
Gaytan, S.P. and Pasaro, R. Neonatal caffeine treatment up-regulates adenosine receptors in brainstem and hypothalamic cardio-respiratory related nuclei of rat pups. Exp Neurol. 2012; 237: 247–259
View in Article | CrossRef | PubMed | Scopus (8)
Laurienti, P.J., Field, A.S., Burdette, J.H., Maldjian, J.A., Yen, Y.F., and Moody, D.M. Dietary caffeine consumption modulates fMRI measures. Neuroimage. 2002; 17: 751–757
View in Article | CrossRef | PubMed
Schultz, K.D., Fritschka, E., Kribben, A., Rothschild, M., Thiede, H.M., Distler, A. et al. Alpha 2- and beta 2-adrenoceptor downregulation in marathon runners. J Hypertens Suppl. 1989; 7: S48–S49
View in Article | CrossRef | PubMed
Rengo, G., Leosco, D., Zincarelli, C., Marchese, M., Corbi, G., Liccardo, D. et al. Adrenal GRK2 lowering is an underlying mechanism for the beneficial sympathetic effects of exercise training in heart failure. Am J Physiol Heart Circ Physiol. 2010; 298: H2032–H2038
View in Article | CrossRef | PubMed | Scopus (44)
Bernstein, D., Fajardo, G., and Zhao, M. The role of beta-adrenergic receptors in heart failure: differential regulation of cardiotoxicity and cardioprotection. Prog Pediatr Cardiol. 2011; 31: 35–38
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (8)
Bond, R.A. Is paradoxical pharmacology a strategy worth pursuing?. Trends Pharmacol Sci. 2001; 22: 273–276
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (45)
Heilbrunn, S.M., Shah, P., Bristow, M.R., Valantine, H.A., Ginsburg, R., and Fowler, M.B. Increased beta-receptor density and improved hemodynamic response to catecholamine stimulation during long-term metoprolol therapy in heart failure from dilated cardiomyopathy. Circulation. 1989; 79: 483–490
View in Article | CrossRef | PubMed
Bond, R.A., Spina, D., Parra, S., and Page, C.P. Getting to the heart of asthma: can “beta blockers” be useful to treat asthma?. Pharmacol Ther. 2007; 115: 360–374
View in Article | CrossRef | PubMed | Scopus (29)
Loffing, J. Paradoxical antidiuretic effect of thiazides in diabetes insipidus: another piece in the puzzle. J Am Soc Nephrol. 2004; 15: 2948–2950
View in Article | CrossRef | PubMed | Scopus (18)
Page, C. Paradoxical pharmacology: turning our pharmacological models upside down. Trends Pharmacol Sci. 2011; 32: 197–200
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (6)
Yun, A.J., Lee, P.Y., and Bazar, K.A. Paradoxical strategy for treating chronic diseases where the therapeutic effect is derived from compensatory response rather than drug effect. Med Hypotheses. 2005; 64: 1050–1059
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (17)
Teixeira, M.Z. Homeopathic use of modern medicines: utilisation of the curative rebound effect. Med Hypotheses. 2003; 60: 276–283
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (19)
Nussinov, R. and Tsai, C.J. Unraveling structural mechanisms of allosteric drug action. Trends Pharmacol Sci. 2014; 35: 256–264
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (10)
Bu, Z. and Callaway, D.J. Proteins move! Protein dynamics and long-range allostery in cell signaling. Adv Protein Chem Struct Biol. 2011; 83: 163–221
View in Article | CrossRef | PubMed | Scopus (23)
Nussinov, R., Ma, B., Tsai, C.J., and Csermely, P. Allosteric conformational barcodes direct signaling in the cell. Structure. 2013; 21: 1509–1521
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (14)
Nussinov, R. and Tsai, C.J. Allostery in disease and in drug discovery. Cell. 2013; 153: 293–305
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (60)
Bellavite, P., Corso, F., Dusi, S., Grzeskowiak, M., Della-Bianca, V., and Rossi, F. Activation of NADPH-dependent superoxide production in plasma membrane extracts of pig neutrophils by phosphatidic acid. J Biol Chem. 1988; 263: 8210–8214
View in Article | PubMed
Swardfager, W., Herrmann, N., McIntyre, R.S., Mazereeuw, G., Goldberger, K., Cha, D.S. et al. Potential roles of zinc in the pathophysiology and treatment of major depressive disorder. Neurosci Biobehav Rev. 2013; 37: 911–929
View in Article | CrossRef | PubMed | Scopus (13)
Ciolek, J., Maiga, A., Marcon, E., Servent, D., and Gilles, N. Pharmacological characterization of zinc and copper interaction with the human alpha(1A)-adrenoceptor. Eur J Pharmacol. 2011; 655: 1–8
View in Article | CrossRef | PubMed | Scopus (4)
del, S.A., Tsai, C.J., Ma, B., and Nussinov, R. The origin of allosteric functional modulation: multiple pre-existing pathways. Structure. 2009; 17: 1042–1050
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (154)
Nussinov, R., Tsai, C.J., and Csermely, P. Allo-network drugs: harnessing allostery in cellular networks. Trends Pharmacol Sci. 2011; 32: 686–693
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (53)
Nussinov, R., Tsai, C.J., and Ma, B. The underappreciated role of allostery in the cellular network. Annu Rev Biophys. 2013; 42: 169–189
View in Article | CrossRef | PubMed | Scopus (30)
Kolomytkin, O.V., Dunn, S., Hart, F.X., Frilot, C., Kolomytkin, D., and Marino, A.A. Glycoproteins bound to ion channels mediate detection of electric fields: a proposed mechanism and supporting evidence. Bioelectromagnetics. 2007; 28: 379–385
View in Article | CrossRef | PubMed | Scopus (13)
Vincze, G., Szasz, A., and Liboff, A.R. New theoretical treatment of ion resonance phenomena. Bioelectromagnetics. 2008; 29: 380–386
View in Article | CrossRef | PubMed | Scopus (11)
Fesenko, E.E. and Gluvstein, A.Y. Changes in the state of water, induced by radiofrequency electromagnetic fields. FEBS Lett. 1995; 367: 53–55
View in Article | Abstract | Full Text PDF | PubMed | Scopus (70)
Del Giudice, E. and Tedeschi, A. Water and autocatalysis in living matter. Electromagn Biol Med. 2009; 28: 46–52
View in Article | CrossRef | PubMed | Scopus (22)
Khesbak, H., Savchuk, O., Tsushima, S., and Fahmy, K. The role of water H-bond imbalances in B-DNA substate transitions and peptide recognition revealed by time-resolved FTIR spectroscopy. J Am Chem Soc. 2011; 133: 5834–5842
View in Article | CrossRef | PubMed | Scopus (8)
Fuxreiter, M., Mezei, M., Simon, I., and Osmany, R. Interfacial water as a ‘hydration fingerprint’ in the noncognate complex of BamHI. Biophys J. 2005; 89: 903–911
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (29)
Freier, E., Wolf, S., and Gerwert, K. Proton transfer via a transient linear water-molecule chain in a membrane protein. Proc Natl Acad Sci U S A. 2011; 108: 11435–11439
View in Article | CrossRef | PubMed | Scopus (56)
Szolnoki, Z. A dynamically changing intracellular water network serves as a universal regulator of the cell: the water-governed cycle. Biochem Biophys Res Commun. 2007; 357: 331–334
View in Article | CrossRef | PubMed | Scopus (9)
Rimratchada, S., McLeish, T.C., Radford, S.E., and Paci, E. The role of high-dimensional diffusive search, stabilization, and frustration in protein folding. Biophys J. 2014; 106: 1729–1740
View in Article | Abstract | Full Text | Full Text PDF | PubMed
Tsai, C.J. and Nussinov, R. The free energy landscape in translational science: how can somatic mutations result in constitutive oncogenic activation?. Phys Chem Chem Phys. 2014; 16: 6332–6341
View in Article | CrossRef | PubMed | Scopus (4)
Strohle, A. and Holsboer, F. Stress responsive neurohormones in depression and anxiety. Pharmacopsychiatry. 2003; 36: S207–S214
View in Article | PubMed
Muchmore, D.B. Raloxifene: a selective estrogen receptor modulator (SERM) with multiple target system effects. Oncologist. 2000; 5: 388–392
View in Article | CrossRef | PubMed
Venard, C., Boujedaini, N., Belon, P., Mensah-Nyagan, A.G., and Patte-Mensah, C. Regulation of neurosteroid allopregnanolone biosynthesis in the rat spinal cord by glycine and the alkaloidal analogs strychnine and gelsemine. Neuroscience. 2008; 153: 154–161
View in Article | CrossRef | PubMed | Scopus (26)
Marzotto, M., Conforti, A., Magnani, P., Zanolin, M.E., and Bellavite, P. Effects of Ignatia amara in mouse behavioural models. Homeopathy. 2012; 101: 57–67
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (5)
Bellavite, P., Marzotto, M., Olioso, D., Moratti, E., and Conforti, A. High-dilution effects revisited. 1. Physicochemical aspects. Homeopathy. 2014; 103: 4–21
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (6)
Van Wijk, R. and Wiegant, F.A. The similia principle as a therapeutic strategy: a research program on stimulation of self-defense in disordered mammalian cells. Altern Ther Health Med. 1997; 3: 33–38
View in Article | PubMed
Bellavite, P., Olioso, D., Marzotto, M., Moratti, E., and Conforti, A. A dynamic network model of the similia principle. Complement Ther Med. 2013; 21: 750–761
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (2)
Zhang, Q., Bhattacharya, S., and Andersen, M.E. Ultrasensitive response motifs: basic amplifiers in molecular signalling networks. Open Biol. 2013; 3: 130031
View in Article | CrossRef | PubMed | Scopus (22)
Bellavite, P. Complexity science and homeopathy. A synthetic overview. Homeopathy. 2003; 92: 203–212
View in Article | Abstract | Full Text | Full Text PDF | PubMed | Scopus (42)

  • Julio Solórzano

    Tha´s why it really works for you and most of the people don´t know it.

  • Elaine McFarland

    Wow this is really exciting research!

  • Nabakrishna Deb Nath

    Thnks for sharing