| Literature DB >> 28837763 |
Hideshi Ihara1, Shingo Kasamatsu1,2, Atsushi Kitamura1, Akira Nishimura2, Hiroyasu Tsutsuki3, Tomoaki Ida2, Kento Ishizaki1, Takashi Toyama4, Eiko Yoshida4, Hisyam Abdul Hamid2,5, Minkyung Jung2, Tetsuro Matsunaga2, Shigemoto Fujii2, Tomohiro Sawa3, Motohiro Nishida6, Yoshito Kumagai4, Takaaki Akaike2.
Abstract
Electrophiles such as methylmercury (MeHg) affect cellular functions by covalent modification with endogenous thiols. Reactive persulfide species were recently reported to mediate antioxidant responses and redox signaling because of their strong nucleophilicity. In this study, we used MeHg as an environmental electrophile and found that exposure of cells to the exogenous electrophile elevated intracellular concentrations of the endogenous electrophilic molecule 8-nitroguanosine 3',5'-cyclic monophosphate (8-nitro-cGMP), accompanied by depletion of reactive persulfide species and 8-SH-cGMP which is a metabolite of 8-nitro-cGMP. Exposure to MeHg also induced S-guanylation and activation of H-Ras followed by injury to cerebellar granule neurons. The electrophile-induced activation of redox signaling and the consequent cell damage were attenuated by pretreatment with a reactive persulfide species donor. In conclusion, exogenous electrophiles such as MeHg with strong electrophilicity impair the redox signaling regulatory mechanism, particularly of intracellular reactive persulfide species and therefore lead to cellular pathogenesis. Our results suggest that reactive persulfide species may be potential therapeutic targets for attenuating cell injury by electrophiles.Entities:
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Year: 2017 PMID: 28837763 DOI: 10.1021/acs.chemrestox.7b00120
Source DB: PubMed Journal: Chem Res Toxicol ISSN: 0893-228X Impact factor: 3.739