Mercury in the body produces a selenium deficiency state that increases toxicity.
Spiller HA. Rethinking mercury: the role of selenium in the pathophysiology of mercury toxicity. Clinical Toxicology. 2018;56(5):313-326.
This study makes the case that mercury’s multifaceted interactions with selenium are a central feature of mercury toxicity. The authors argue that “the previously suggested ‘protective effect’ of selenium against mercury toxicity may in fact be backwards”—because of mercury’s affinity for selenium, mercury can actually produce a selenium deficiency state that promotes oxidative stress and inhibits the body’s regenerative mechanisms. Depending on the form of mercury and other factors, selenium supplementation may have some benefits for restoring adequate selenium status and mitigating the toxicity of mercury, but it does not appear to promote increased elimination of mercury.
Alternatively spliced methionine synthase in SH-SY5Y neuroblastoma cells: Cobalamin and GSH dependence and inhibitory effects of neurotoxic metals and thimerosal
Thimerosal reduces people’s ability to make all-important vitamin B12 compounds that help the body detoxify and control inflammation—and B12 deficiencies and severely impaired detoxification are hallmarks of autism.
Waly M, Power-Charnitsky V-A, Hodgson N, … Deth R. Oxidative Medicine and Cellular Longevity. 2016, Article ID 6143753.
Thimerosal inhibited cellular production of cobalamin necessary for detoxification and amelioration of oxidative stress. This caused lower methionine synthase activity and an impaired methylation capacity. Autistic subjects in general show cobalamin deficiencies and severely impaired methylation.
Thimerosal Neurotoxicity is Associated with Glutathione Depletion: Protection with Glutathione Precursors
Vaccine mercury depletes a vital antioxidant, glutathione.
S.J. James, William Slikker, Stepan Melnyk, Elizabeth New,
Marta Pogribna, Stefanie Jernigan. NeuroToxicology, 26 (2005) 1–8.
“Thimerosal is an antiseptic containing 49.5% ethyl mercury that has been used for years as a preservative in many infant vaccines and in flu vaccines. Environmental methyl mercury has been shown to be highly neurotoxic, especially to the developing brain. Because mercury has a high affinity for thiol (sulfhydryl (-SH)) groups, the thiol-containing antioxidant, glutathione (GSH), provides the major intracellular defense against mercury-induced neurotoxicity. Cultured neuroblastoma cells were found to have lower levels of GSH and increased sensitivity to thimerosal toxicity compared to glioblastoma cells that have higher basal levels of intracellular GSH. Thimerosal-induced cytotoxicity was associated with depletion of intracellular GSH in both cell lines. Although Thimerosal has been recently removed from most children’s vaccines, it is still present in flu vaccines given to pregnant women, the elderly, and to children in developing countries.”