
Thiosulfate Mediates Cytoprotective Effects of Hydrogen Sulfide Against Neuronal Ischemia
Author(s) -
Marutani Eizo,
Yamada Marina,
Ida Tomoaki,
Tokuda Kentaro,
Ikeda Kohei,
Kai Shinichi,
Shirozu Kazuhiro,
Hayashida Kei,
Kosugi Shizuko,
Hanaoka Kenjiro,
Kaneki Masao,
Akaike Takaaki,
Ichinose Fumito
Publication year - 2015
Publication title -
journal of the american heart association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.494
H-Index - 85
ISSN - 2047-9980
DOI - 10.1161/jaha.115.002125
Subject(s) - sodium thiosulfate , thiosulfate , neuroprotection , medicine , pharmacology , sodium hydrosulfide , ischemia , hydrogen sulfide , programmed cell death , apoptosis , biochemistry , sulfur , biology , chemistry , inorganic chemistry , organic chemistry
Background Hydrogen sulfide (H 2 S) exhibits protective effects in various disease models including cerebral ischemia–reperfusion (I/R) injury. Nonetheless, mechanisms and identity of molecules responsible for neuroprotective effects of H 2 S remain incompletely defined. In the current study, we observed that thiosulfate, an oxidation product of H 2 S, mediates protective effects of an H 2 S donor compound sodium sulfide (Na 2 S) against neuronal I/R injury. Methods and Results We observed that thiosulfate in cell culture medium is not only required but also sufficient to mediate cytoprotective effects of Na 2 S against oxygen glucose deprivation and reoxygenation of human neuroblastoma cell line ( SH ‐ SY 5Y) and murine primary cortical neurons. Systemic administration of sodium thiosulfate ( STS ) improved survival and neurological function of mice subjected to global cerebral I/R injury. Beneficial effects of STS , as well as Na 2 S, were associated with marked increase of thiosulfate, but not H 2 S, in plasma and brain tissues. These results suggest that thiosulfate is a circulating “carrier” molecule of beneficial effects of H 2 S. Protective effects of thiosulfate were associated with inhibition of caspase‐3 activity by persulfidation at Cys163 in caspase‐3. We discovered that an SLC 13 family protein, sodium sulfate cotransporter 2 ( SLC 13A4, NaS‐2), facilitates transport of thiosulfate, but not sulfide, across the cell membrane, regulating intracellular concentrations and thus mediating cytoprotective effects of Na 2 S and STS . Conclusions The protective effects of H 2 S are mediated by thiosulfate that is transported across cell membrane by NaS‐2 and exerts antiapoptotic effects via persulfidation of caspase‐3. Given the established safety track record, thiosulfate may be therapeutic against ischemic brain injury.