A cholesterol and actinide dependent shadow biosphere of archaea and viroids in autoimmune diseases
Immunobiology, ISSN: 0171-2985, Vol: 217, Issue: 3, Page: 316-320
2012
- 2Citations
- 17Captures
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Article Description
Endogenous digoxin has been related to the pathogenesis of multiple sclerosis and other autoimmune diseases like systemic lupus erythematosis and rheumatoid arthritis. The possibility of endogenous digoxin synthesis by archaea with a mevalonate pathway and cholesterol catabolism was considered. 10 cases each of multiple sclerosis and other autoimmune diseases like systemic lupus erythematosis and rheumatoid arthritis before starting treatment and 10 age and sex matched healthy controls from general population were chosen for the study. Cholesterol substrate was added to the plasma of the patients and the generation of cytochrome F420, free RNA, free DNA, polycyclic aromatic hydrocarbon, hydrogen peroxide, serotonin, pyruvate, ammonia, glutamate, cytochrome C, hexokinase, ATP synthase, HMG CoA reductase, digoxin and bile acids were studied. The changes with the addition of antibiotics and cerium to the patient's plasma were also studied. The statistical analysis was done by ANOVA. The parameters mentioned above were increased the patient's plasma with addition of cholesterol substrate. The addition of antibiotics to the patient's plasma caused a decrease in all the parameters while addition of cerium increased their levels. An actinide dependent shadow biosphere of archaea and viroids is described in multiple sclerosis and other autoimmune diseases like systemic lupus erythematosis and rheumatoid arthritis contributing to their pathogenesis.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0171298511002154; http://dx.doi.org/10.1016/j.imbio.2011.10.005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84856443912&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/22137029; https://linkinghub.elsevier.com/retrieve/pii/S0171298511002154; https://dx.doi.org/10.1016/j.imbio.2011.10.005
Elsevier BV
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