Modulation of Signal Proteins: A Plausible Mechanism to Explain How a Potentized Drug Secale Cor 30C Diluted beyond Avogadro's Limit Combats Skin Papilloma in Mice

Hindawi Publishing Corporation | Evidence-Based Complementary and Alternative Medicine | Volume 2011, Article ID 286320, 12 pagesModulation of Signal Proteins: A PlausibleMechanism to Explain How a Potentized Drug Secale Cor 30C Diluted beyond Avogadro's Limit Combats Skin Papilloma in MiceAnisur Rahman Khuda-Bukhsh,1 Soumya Sundar Bhattacharyya,1 Saili Paul,1 Suman Dutta,1 Naoual Boujedaini,2 and Philippe Belon2

1.Cytogenetics and Molecular Biology Laboratory, Department of Zoology, University of Kalyani, Kalyani 741235, West Bengal, India 2.Boiron Laboratory, Lyon, France

Copyright © 2011 Anisur Rahman Khuda-Bukhsh et al. This is an open access article.

In homeopathy, ability of ultra-high diluted drugs at or above potency 12C (diluted beyond Avogadro's limit) in ameliorating/curing various diseases is often questioned, particularly because the mechanism of action is not precisely known. We tested the hypothesis if suitable modulations of signal proteins could be one of the possible pathways of action of a highly diluted homeopathic drug, Secale cornutum 30C (diluted 1060 times; Sec cor 30). It could successfully combat DMBA + croton oilinduced skin papilloma in mice as evidenced by histological, cytogenetical, immunofluorescence, ELISA and immunoblot findings. Critical analysis of several signal proteins like AhR, PCNA, Akt, Bcl-2, Bcl-xL, NF-κB and IL-6 and of pro-apoptotic proteins like cytochrome c, Bax, Bad, Apaf, caspase-3 and -9 revealed that Sec cor 30 suitably modulated their expression levels along with amelioration of skin papilloma. FACS data also suggested an increase of cell population at S and G2 phases and decrease in sub- G1 and G1 phages in carcinogen-treated drug-unfed mice, but these were found to be near normal in the Sec cor 30-fed mice. There was reduction in genotoxic and DNA damages in bone marrow cells of Sec Cor 30-fed mice, as revealed from cytogenetic and Comet assays. Changes in histological features of skin papilloma were noted. Immunofluorescence studies of AhR and PCNA also suggested reduced expression of these proteins in Sec cor 30-fed mice, thereby showing its anti-cancer potentials against skin papilloma. Furthermore, this study also supports the hypothesis that potentized homeopathic drugs act at gene regulatory level.

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n late 2011, the Swiss government's report on homeopathic medicine represents the most comprehensive evaluation of homeopathic medicine ever written by a government

The Swiss government has a long and widely-respected history of neutrality, and therefore, reports from this government on controversial subjects need to be taken more seriously than other reports from countries that are more strongly influenced by present economic and political constituencies. When one considers that two of the top five largest drug companies in the world have their headquarters in Switzerland, one might assume that this country would have a heavy interest in and bias toward conventional medicine, but such assumptions would be wrong.  In late 2011, the Swiss government's report on homeopathic medicine represents the most comprehensive evaluation of homeopathic medicine ever written by a government and was just published in book form in English (Bornhoft and Matthiessen, 2011). This breakthrough report affirmed that homeopathic treatment is both effective and cost-effective and that homeopathic treatment should be reimbursed by Switzerland's national health insurance program. 

The Swiss government's inquiry into homeopathy and complementary and alternative (CAM) treatments resulted from the high demand and widespread use of alternatives to conventional medicine in Switzerland, not only from consumers but from physicians as well. Approximately half of the Swiss population have used CAM treatments and value them. Further, about half of Swiss physicians consider CAM treatments to be effective. Perhaps most significantly, 85 percent of the Swiss population wants CAM therapies to be a part of their country's health insurance program. 

It is therefore not surprising that more than 50 percent of the Swiss population surveyed prefer a hospital that provides CAM treatments rather to one that is limited to conventional medical care. 

Beginning in 1998, the government of Switzerland decided to broaden its national health insurance to include certain complementary and alternative medicines, including homeopathic medicine, traditional Chinese medicine, herbal medicine, anthroposophic medicine, and neural therapy. This reimbursement was provisional while the Swiss government commissioned an extensive study on these treatments to determine if they were effective and cost-effective. The provisional reimbursement for these alternative treatments ended in 2005, but as a result of this new study, the Swiss government's health insurance program once again began to reimburse for homeopathy and select alternative treatments. In fact, as a result of a national referendum in which more than two-thirds of voters supported the inclusion of homeopathic and select alternative medicines in Switzerland's national health care insurance program, the field of complementary and alternative medicine has become a part of this government's constitution (Dacey, 2009; Rist, Schwabl, 2009). 

The Swiss Government's "Health Technology Assessment" 

The Swiss government's "Health Technology Assessment" on homeopathic medicine is much more comprehensive than any previous governmental report written on this subject to date. Not only did this report carefully and comprehensively review the body of evidence from randomized double-blind and placebo controlled clinical trials testing homeopathic medicines, they also evaluated the "real world effectiveness" as well as safety and cost-effectiveness. The report also conducted a highly-comprehensive review of the wide body of preclinical research (fundamental physio-chemical research, botanical studies, animal studies, and in vitro studies with human cells). 

And still further, this report evaluated systematic reviews and meta-analyses, outcome studies, and epidemiological research. This wide review carefully evaluated the studies conducted, both in terms of quality of design and execution (called "internal validity") and how appropriate each was for the way that homeopathy is commonly practiced (called "external validity"). The subject of external validity is of special importance because some scientists and physicians conduct research on homeopathy with little or no understanding of this type of medicine (some studies tested a homeopathic medicine that is rarely used for the condition tested, while others utilized medicines not commonly indicated for specific patients). When such studies inevitably showed that the homeopathic medicine did not "work," the real and accurate assessment must be that the studies were set up to disprove homeopathy... or simply, the study was an exploratory trial that sought to evaluate the results of a new treatment (exploratory trials of this nature are not meant to prove or disprove the system of homeopathy but only to evaluate that specific treatment for a person with a specific condition). 

After assessing pre-clinical basic research and the high quality clinical studies, the Swiss report affirmed that homeopathic high-potencies seem to induce regulatory effects (e.g., balancing or normalizing effects) and specific changes in cells or living organisms. The report also reported that 20 of the 22 systematic reviews of clinical research testing homeopathic medicines detected at least a trend in favor of homeopathy.* (Bornhöft, Wolf, von Ammon, et al, 2006) 

The Swiss report found a particularly strong body of evidence to support the homeopathic treatment of Upper Respiratory Tract Infections and Respiratory Allergies. The report cited 29 studies in "Upper Respiratory Tract Infections/AllergicReactions," of which 24 studies found a positive result in favor of homeopathy. Further, six out of seven controlled studies that compared homeopathic treatment with conventional medical treatment showed that homeopathy to be more effective than conventional medical interventions (the one other trial found homeopathic treatment to be equivalent to conventional medical treatment). All of these results from homeopathic treatment came without the side effects common to conventional drug treatment. In evaluating only the randomized placebo controlled trials, 12 out of 16 studies showed a positive result in favor of homeopathy. 

The authors of the Swiss government's report acknowledge that a part of the overall review of research included one review of clinical research in homeopathy (Shang, et al, 2005). However, the authors noted that this review of research has been widely and harshly criticized by both advocates and non-advocates of homeopathy. The Swiss report noted that the Shang team did not even adhere to the QUORUM guidelines which are widely recognized standards for scientific reporting (Linde, Jonas, 2005). The Shang team initially evaluated 110 homeopathic clinical trials and then sought to compare them with a matching 110 conventional medical trials. Shang and his team determined that there were 22 "high quality" homeopathic studies but only nine "high quality" conventional medical studies. Rather than compare these high quality trials (which would have shown a positive result for homeopathy), the Shang team created criteria to ignore a majority of high quality homeopathic studies, thereby trumping up support for their original hypothesis and bias that homeopathic medicines may not be effective (Lüdtke, Rutten, 2008). 

The Swiss report also notes that David Sackett, M.D., the Canadian physician who is widely considered to be one of the leading pioneers in "evidence based medicine," has expressed serious concern about those researchers and physicians who consider randomized and double-blind trials as the only means to determine whether a treatment is effective or not. To make this assertion, one would have to acknowledge that virtually all surgical procedures were "unscientific" or "unproven" because so few have undergone randomized double-blind trials. 

In my view, for a treatment to be determined to be "effective" or "scientifically proven," a much more comprehensive assessment of what works and doesn't is required. Ultimately, the Swiss government's report on homeopathy represents an evaluation of homeopathy that included an assessment of randomized double blind trials as well as other bodies of evidence, all of which together lead the report to determine that homeopathic medicines are indeed effective. 

The next article will discuss further evidence provided in this report from the Swiss government on the effectiveness and cost-effectiveness of homeopathic care. 

--- REFERENCES: 

Bornhoft, Gudrun, and Matthiessen, Peter F. Homeopathy in Healthcare: Effectiveness, Appropriateness, Safety, Costs. Goslar, Germany: Springer, 2011. http://rd.springer.com/book/10.1007/978-3-642-20638-2/page/1(This book is presently available from the German office of the publisher, and it will become available via the American office as well as select booksellers in mid- to late-February, 2012.)(NOTE: When specific facts in the above article are provided but not referenced, this means that these facts were derived from this book.) 

Bornhöft G, Wolf U, von Ammon K, Righetti M, Maxion-Bergemann S, Baumgartner S, Thurneysen AE, Matthiessen PF. Effectiveness, safety and cost-effectiveness of homeopathy in general practice - summarized health technology assessment. Forschende Komplementärmedizin (2006);13 Suppl 2:19-29. http://www.ncbi.nlm.nih.gov/pubmed/16883077 

Dacey, Jessica. Therapy supporters roll up sleeves after vote. SwissInfo.ch, May 19, 2009. http://www.swissinfo.ch/eng/politics/Therapy_supporters_roll_up_sleeves_after_vote.html?cid=670064 

Linde K, Jonas W. Are the clinical effects of homeopathy placebo effects? Lancet 36:2081-2082. DOI:10.1016/S0140-6736(05)67878-6. http://download.thelancet.com/pdfs/journals/lancet/PIIS0140673605678786.pdf 

Lüdtke R, Rutten ALB. The conclusions on the effectiveness of homeopathy highly depend on the set of analysed trials. Journal of Clinical Epidemiology. October 2008. doi: 10.1016/j.jclinepi.2008.06/015. http://www.jclinepi.com/article/S0895-4356(08)00190-X/abstract 

Rist L, Schwabl H: Komplementärmedizin im politischen Prozess. Schweizer Bevölkerungstimmt über Verfassungsartikel «Zukunft mit Komplementärmedizin» ab. Forsch Komplementmed 2009, doi 10.1159/000203073. (Translation: Complementary medicine in the political process: The Swiss population votes on the Constitutional Article "The future with complementary medicine" http://www.ayurveda-association.eu/files/swiss_referendum_on_cam_-_forschkomplementmed_2009.pdf 

*Although this Swiss government report was just published in book form in 2011, the report was finalized in 2006. In light of this date, the authors evaluated systematic reviews and meta-analyses on homeopathic research up until June 2003. 

By, Dana Ullman, MPH, is America's leading spokesperson for homeopathy and is the founder of www.homeopathic.com. He is the author of 10 books, including his bestseller, Everybody's Guide to Homeopathic Medicines. His most recent book is, The Homeopathic Revolution: Why Famous People and Cultural Heroes Choose Homeopathy (the Foreword to this book was written by Dr. Peter Fisher, the Physician to Her Majesty Queen Elizabeth II). Dana lives, practices, and writes from Berkeley, California. 

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[Fwd: [HOMEOPATHY] Who is more neutral than the Swiss...]

Who is more neutral than the Swiss...
Dana Ullman 6:40am Feb 15
Who is more neutral than the Swiss government...and this is the most positive report on homeopathy ever published by a government! This is great news...spread the good news! http://www.huffingtonpost.com/dana-ullman/homeopathic-medicine-_b_1258607.html?ref=health-and-fitness&ir=Health+and+Fitness
The Swiss Government's Remarkable Report on Homeopathic Medicine

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The Swiss government's report on homeopathic medicine represents the most comprehensive evaluation o...

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Meningococcal Meningitis in Brazil

The Brazilian ExperienceIn 1998 there was an outbreak of meningococcal meningitis in a region of Brazil. Many doctors in that country are also homeopaths. There was no vaccine available at the time, so a group of doctors who worked in the region used the meningococcal Nosode to immunize 65,826 children. Another 23,539 children in the region were not immunized. The doctors followed the two groups for 12 months. After 6 months the efficacy of homeoprophylaxis was 95%, and after 12 months was 91%. A complete and statistically rigorous report was published in a leading peer reviewed Homeopathic journal, and is available for study (see reference following). Mroninski C, Adriano E, Mattos G (2001) Meningococcinum: Its protective effect against meningococcal disease. Homoeopathic Links Winter Vol 14(4); pp. 230-4. 

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Homeopathy as an alternative to antibiotics in diarrhoea in piglets

Homeopathy as an alternative to antibiotics in diarrhoea in pigletsA research study conducted at the Wageningen University in the Netherlands suggests that homeopathy may be an alternative to antibiotics in neonatal diarrhea of piglets.The overuse of antibiotics in poultry, beef cattle and swine production poses a serious threat to human health, animal health and the environment. Sustainable alternatives to antibiotics are desperately needed.

In the organic livestock sector antibiotics are preferably replaced by complementary or alternative medicines (CAM), of which homeopathy is the most frequently applied. Homeopathic treatment has significant benefits since there are no residues of homeopathic medicines in animal products, nor does homeopathy generate resistant microorganisms.

The Biological Farming Systems Group at the Wageningen University in the Netherlands recently conducted a research study to investigate if homeopathy might be an alternative to antibiotics in one of the most common illnesses in swine which is neonatal diarrhoea of piglets. This disease leads to weight loss and increased piglet mortality, which has substantial economic consequences. Conventional treatments of Escherichia coli (E. coli) diarrhoea is administration of antibiotics to affected piglets, or preventive vaccination of the sows.

To investigate if E. coli diarrhoea in neonatal piglets could be prevented by homeopathy, the researchers set up a randomised, observer blind and placebo-controlled trial. On a commercial pig farm 52 sows of different parities, in their last month of gestation, were treated twice a week with either the homeopathic agent Coli 30K or placebo. The 525 piglets born from these sows were scored for occurrence and duration of diarrhoea.

Piglets of the homeopathic treated group had significantly less E. coli diarrhoea than piglets in the placebo group (P < .0001). Especially piglets from first parity sows gave a good response to treatment with Coli 30K. The diarrhoea seemed to be less severe in the homeopathically treated litters, there was less transmission and duration appeared shorter.

Advantages at farm level are application of the treatment by the farmer and cost reduction. These advantages and the positive results from this study make the homeopathic agent Coli 30K an attractive potential alternative in the prevention of E. coli diarrhoea. This study also suggests that homeopathic treatment in livestock may help the European citizen be protected from pharmacological residues in animal products and thus reduce the problem of antibiotic resistance.

Reference Camerlink I, Ellinger L, Bakker EJ, Lantinga EA (2010). Homeopathy as replacement to antibiotics in the case of Escherichia coli diarrhoea in neonatal piglets. Homeopathy, 99; 57–62.

PubMed abstract can be found here, full article here: http://www.homeopathyeurope.org/media/news/homeopathy-as-an-alternative-to-antibiotics-in-diarrhoea-in-piglets

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Homeopathy Halts Cuban Epidemic Better Than Vaccines

Homeopathy Halts Cuban Epidemic Better Than Vaccines  Swamp fever, also known as leptospirosis, is a major problem in Cuba.  Each year, an epidemic of swamp fever plagues the island nation during the flood season when the illness is transferred from rats to people. 

The very serious symptoms of swamp fever include fever, diarrhea, vomiting, jaundice, meningitis, liver failure, renal damage, respiratory illness and in many cases, death. 

Fortunately for Cuba, Big Pharma is not much interested in monopoly control of its healthcare system which leaves the door open for alternative and nontoxic approaches to health to bloom. 

In this environment very open to homeopathy, the Finlay Institute, a Cuban research foundation, worked with Cuban doctors to develop a homeopathic nosode for swamp fever. 

The remedy was based on the homeopathic principle that “like cures like” and was developed and administered on a wide scale as a preventative treatment.  In 2008, 2.5 million people who were most susceptible to the disease were treated with 2 doses of the remedy seven to nine days apart.   The Cuban Ministry of Public Health implemented and managed the operation. 

The results of this effort were nothing short of spectacular. The typical rate of infection when vaccination and antibiotics are used is a few thousand cases per year including some deaths. 

When the homeopathic remedy was used, however, only ten cases of swamp fever were reported among the 2.5 million treated with the homeopathic nosode with no mortality of any hospitalized patients! 

The financial cost to the Cuban government for this astonishingly successful health campaign was only $200,000 compared with the $2,000,000 that would have been incurred for conventional vaccination and antibiotics. 

Not only was homeopathy clearly more effective than vaccines for preventing swamp fever, it was also a much more cost effective solution with no toxic side effects such as is the case with vaccination. 

Homeopathy for epidemics works.  There is no need for toxic and expensive vaccine injections which produce masses of auto-immune compromised children and adults alike in need and dependent upon – more drugs! 

The catalyst for widespread use of homeopathic nosodes as a safe and effective alternative to the ever growing list of toxic vaccines must come from parents, in particular mothers.  Mothers must refuse toxic vaccines for their children and demand this type of safe and effective remedy at a grassroots level as it will never come from the conventional medical establishment which has a strongly invested profit motive for keeping things the way they are. 

Sarah, The Healthy Home Economist 

http://www.thehealthyhomeeconomist.com/homeopathy-halts-cuban-epidemic-better-than-vaccines/

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The use of Arsenicum album 30c to complement conventional treatment of neonatal diarrhoea (‘scours’) in calves

S. Kayne PhD, MBA, BSC, MRPHARMS, MCPP, DAGVETPHARM, MPSNZ*Corresponding Author Contact Information, A. Rafferty BVMS, CERT CHP, CERT SHP, MRCVS**

Available online 5 September 2006.

Abstract

In a pilot double blind study carried out in Scotland, the effect of supplementing a conventional treatment plan with homoeopathic Arsenicum albumwas studied. In the management of neonatal calf scour it appeared that more animals recovered after one day in the group that had received active medicine, than in the placebo group. These results are encouraging.

Keywords: Scours; Arsenicum album; Calves; Diarrhoea; neonatal; Veterinary medicine

Corresponding Author Contact InformationAddress for correspondence Dr S. B. Kayne 79 Milverton Road Giffnock Glasgow G46 7LQ

*Lecturer in homoeopathic pharmacy, Academic Department of Homoeopathic Medicine, Glasgow Homoeopathic Hospital.

**Veterinary Surgeon.

Inhibition of basophil activation by histamine: a sensitive and reproducible model for the study of the biological activity of high dilutions

Inhibition of basophil activation by histamine: a sensitive and reproducible model for the study of the biological activity of high dilutions

J. Sainte-Laudy1Corresponding Author Contact InformationE-mail The Corresponding Author, Ph Belon2

 

Received 8 July 2009; revised 21 September 2009; Accepted 23 September 2009. Available online 27 November 2009.

Background

At the beginning of this series of experiments we were looking for a model based on the use of purified commercially available compounds based on a fully described and accepted pharmacological model to study of the biological effect of high dilutions. Negative feedback induced by histamine, a major pro-inflammatory mediator, on basophils and mast cells activation via an H2 receptor me these criteria. The simplest way of measuring basophil activation in the early 1980's was the human basophil activation test (HBDT).

Objectives

Our major goal was first to study the biological effect of centesimal histamine dilutions beyond the Avogadro limit, on the staining properties of human basophils activated by an allergen extract initially house dust mite, then an anti-IgE and N-formyl-Met-Leu-Phe (fMLP). Technical development over the 25 years of our work led us to replace the manual basophil counting by flow cytometry. The main advantages were automation and observer independence. Using this latter protocol our aim was to confirm the existence of this phenomenon and to check its specificity by testing, under the same conditions, inactive analogues of histamine and histamine antagonists. More recently, we developed an animal model (mouse basophils) to study the effect of histamine on histamine release.

Methods and results

For the HBDT model basophils were obtained by sedimentation of human blood taken on EDTA and stained with Alcian blue. Results were expressed in percentage activation. Histamine dilutions tested were freshly prepared in the lab by successive centesimal dilutions and vortexing. Water controls were prepared in the same way. For the flow cytometric protocol basophils were first labeled by an anti-IgE FITC (basophil marker) and an anti-CD63 (basophil activation marker). Results were expressed in percentage of CD63 positive basophils. Another flow cytometric protocol has been developed more recently, based on basophil labeling by anti-IgE FITC (fluorescein isothiocyanate) and anti-CD203 PE (another human basophil activation marker). Results were expressed in mean fluorescence intensity of the CD203c positive population (MFI-CD203c) and an activation index calculated by an algorithm. For the mouse basophil model, histamine was measured spectrofluorimetrically.

The main results obtained over 28 years of work was the demonstration of a reproducible inhibition of human basophil activation by high dilutions of histamine, the effect peaks in the range of 15–17CH. The effect was not significant when histamine was replaced by histidine (a histamine precursor) or cimetidine (histamine H2 receptor antagonist) was added to the incubation medium. These results were confirmed by flow cytometry. Using the latter technique, we also showed that 4-Methyl histamine (H2 agonist) induced a similar effect, in contrast to 1-Methyl histamine, an inactive histamine metabolite.

Using the mouse model, we showed that histamine high dilutions, in the same range of dilutions, inhibited histamine release.

Conclusions

Successively, using different models to study of human and murine basophil activation, we demonstrated that high dilutions of histamine, in the range of 15–17CH induce a reproducible biological effect. This phenomenon has been confirmed by a multi-center study using the HBDT model and by at least three independent laboratories by flow cytometry. The specificity of the observed effect was confirmed, versus the water controls at the same dilution level by the absence of biological activity of inactive compounds such as histidine and 1-Methyl histamine and by the reversibility of this effect in the presence of a histamine receptor H2 antagonist.

Keywords: Human basophil; Mouse basophil; High dilutions; Homoeopathy; Histamine; Flow cytometry; Histamine release; IL4 release

http://www.sciencedirect.com/science/article/pii/S1475491609000952

Homeopathic Arnica montana for post-tonsillectomy analgesia: a randomised placebo control trial

Homeopathic Arnica montana for post-tonsillectomy analgesia: a randomised placebo control trial A. Robertson1, R. Suryanarayanan2, Corresponding Author Contact Information, E-mail The Corresponding Author, A Banerjee3 Purchase 1 ENT Department, University Hospital of Wales, Cardiff, UK 2 ENT Department, Arrowe Park Hospital, Wirral, UK 3 ENT Department, Leicester Royal Infirmary, Leicester, UK Received 19 June 2006; revised 3 August 2006; Accepted 30 October 2006. Available online 14 January 2007.

Abstract Objective: To evaluate the efficacy of Homeopathic Arnica in reducing the morbidity following tonsillectomy

Methods: Randomised double blind, placebo controlled trial at a tertiary referral centre. 190 patients over the age of 18 undergoing tonsillectomy were randomised into intervention and control groups receiving either Arnica 30c or identical placebo, 2 tablets 6 times in the first post-operative day and then 2 tablets twice a day for the next 7 days. The primary outcome measure was the change in pain scores (visual analogue scale) recorded by the patient on a questionnaire over 14 days post-operatively; Secondary outcome measures were: analgesia consumption, visits to the GP or hospital, antibiotic usage, the day on which their swallowing returned to normal and the day on which they returned to work. Results: 111 (58.4%) completed questionnaires were available for analysis. The Arnica group had a significantly larger drop in pain score from day 1 to day 14 (28.3) compared to the placebo group (23.8) with p<0.05. The two groups did not differ significantly on analgesic consumption or any of the other secondary outcome measures (number of post-operative visits to GP, use of antibiotics and secondary haemorrhage readmissions).

Conclusion: The results of this trial suggest that Arnica montana given after tonsillectomy provides a small, but statistically significant, decrease in pain scores compared to placebo. Keywords: homeopathy; surgery; pain management; tonsillectomy

Homeopathic and integrative treatment for feline hyperthyroidism – four cases (2006–2010)

Sara Fox Chapman Corresponding Author Contact InformationE-mail The Corresponding Author

Purchase

The Animal Medical Center of Watkins Park, PO Box 426, Cheltenham, MD 20623, USA

Received 7 February 2011; revised 13 May 2011; Accepted 24 May 2011. Available online 28 September 2011.

Hyperthyroidism is a frequent veterinary problem, particularly in elderly cats. Homeopathic treatment and other integrative modalities were provided for four hyperthyroid cats whose owners did not want conventional treatment. Symptomatic homeopathic treatment with Thyroidinum was helpful in one cat. All cats were prescribed an appropriate individualized homeopathic remedy. All four cats showed resolution of clinical signs; three attained normal thyroid hormone levels. Three cats later received acupuncture and/or herbal medicines; two cats later received symptomatic homeopathic remedies. Two cats are thriving after over 3.5 and 4.25 years of treatment; two were euthanized for unrelated problems after 3 and 4 years of treatment. Homeopathic and complementary therapies avoid the potential side effects of methimazole and surgical thyroidectomy, they are less costly than radioactive iodine treatment, and they provide an option for clients who decline conventional therapies.

Keywords: Hyperthyroidism; Feline; Thyroidinum; Constitutional; Individualized; Veterinary; Homeopathy

Ultra High Dilution of triiodothyronine modifies cellular apoptosis in Rana catesbeiana tadpole tail in vitro

J.R.P. Guedes1Corresponding Author Contact InformationE-mail The Corresponding Author, S. Carrasco2, C.M. Ferreira3, L.V. Bonamin45, W. Souza1, C. Goldenstein-Schainberg2, E.R. Parra1, V.L. Capelozzi1

 

Received 14 June 2010; revised 27 April 2011; Accepted 6 May 2011. Available online 28 September 2011.

Background

Ultra High Dilutions (UHD) are diluted beyond the Avogadro limit with dynamization (dilution with succussion). The process of anuran amphibian metamorphosis is controlled by thyroid hormones, including the resorption of the tadpole tail.

Methods

A randomized and blinded study was performed to investigate the influence of triiodothyronine (T3) 5 · 10−24 M (10cH) on apoptosis induced by T3 100 nM in Rana catesbeiana tadpoles’ tail tips, in vitro. Explants were randomized to three groups: control: no T3 in pharmacological or UHD dose; test: T3 100 nM and challenged with T3 10cH (UHD); positive control: T3 100 nM, treated with unsuccussed ethanol. The apoptotic index and the area of explants of test and control groups at the first and final day of the experiment were compared by t-test.

Results

There was no difference in tail tip area between test and control groups, but a significantly higher (p < 0.01) index of apoptosis in explants of the test group.

Conclusion

This data suggest that T3 10cH modifies the effect of T3 at pharmacological dose, opening new perspectives for further studies and investigation of the dose–effect curve.

Keywords: Ultra High Dilution; Triiodothyronine; Apoptosis; Rana catesbeiana; Organ culture; Metamorphosis; Endo-isopathy; Homeopathy

Influence of Potassium Dichromate on Tracheal Secretions in Critically Ill Patients*

Influence of Potassium Dichromate on Tracheal Secretions in Critically Ill Patients*Michael Frass, MD; Christoph Dielacher, RN; Manfred Linkesch, MD; Christian Endler, PhD; Ilse Muchitsch, PhD; Ernst Schuster, PhD; and Alan Kaye, MD Background: Stringy, tenacious tracheal secretions may prevent extubation in patients weaned from the respirator. This prospective, randomized, double-blind, placebo-controlled study with parallel assignment was performed to assess the influence of sublingually administered potassium dichromate C30 on the amount of tenacious, stringy tracheal secretions in critically ill patients with a history of tobacco use and COPD. Methods: In this study, 50 patients breathing spontaneously with continuous positive airway pressure were receiving either potassium dichromate C30 globules (group 1) [Deutsche Ho- mo ̈opathie-Union, Pharmaceutical Company; Karlsruhe, Germany] or placebo (group 2). Five globules were administered twice daily at intervals of 12 h. The amount of tracheal secretions on day 2 after the start of the study as well as the time for successful extubation and length of stay in the ICU were recorded. Results: The amount of tracheal secretions was reduced significantly in group 1 (p < 0.0001). Extubation could be performed significantly earlier in group 1 (p < 0.0001). Similarly, length of stay was significantly shorter in group 1 (4.20 􏰀 1.61 days vs 7.68 􏰀 3.60 days, p < 0.0001 [mean 􏰀 SD]). Conclusion: These data suggest that potentized (diluted and vigorously shaken) potassium dichromate may help to decrease the amount of stringy tracheal secretions in COPD patients. (CHEST 2005; 127:936–941) Key words: COPD; double-blind, randomized, placebo-controlled study; extubation; homeopathy; tracheal secretions Abbreviations: APACHE 􏰁 acute physiology and chronic health evaluation; BMI 􏰁 body mass index; CPAP 􏰁 con- tinuous positive airway pressure; Fio2 􏰁 fraction of inspired oxygen