摘要

<jats:p> The emergence of hydrogen sulfide (H <jats:sub>2</jats:sub> S) as a new signalling molecule able to control vasodilation, neurotransmission and immune response, prompted questions about its possible cross-talk with the other gasontransmitter, nitric oxide (NO). It has been shown that H <jats:sub>2</jats:sub> S reacts with NO and its metabolites and several potentially biologically active species have been identified. Thionitrous acid (HSNO) was proposed to be an intermediate product of the reaction of <jats:italic>S</jats:italic> -nitrosothiols with H <jats:sub>2</jats:sub> S capable of crossing the membranes and causing further trans-nitrosation of proteins. Alternatively, formation of nitrosopersulfide (SSNO <jats:sup>−</jats:sup> ) has been proposed in this reaction. SSNO <jats:sup>−</jats:sup> was claimed to be particularly stable and inert to H <jats:sub>2</jats:sub> S, thiols and cyanides. It is suggested that this putative SSNO <jats:sup>−</jats:sup> slowly decomposes to give NO, HNO and polysulfides. However, the chemical studies with pure SSNO <jats:sup>−</jats:sup> salts showed some conflicting observations. In this study, we work with pure PNP <jats:sup>+</jats:sup> SSNO <jats:sup>−</jats:sup> to show that contrary to everything that is claimed for the yellow reaction product of GSNO with H <jats:sub>2</jats:sub> S, pure SSNO <jats:sup>−</jats:sup> decomposes readily in the presence of cyanide, H <jats:sub>2</jats:sub> S and glutathione to form SNO <jats:sup>−</jats:sup> . Based on literature overview and chemical data about the structures of HSNO/SNO <jats:sup>−</jats:sup> and SSNO <jats:sup>−</jats:sup> we discuss the biological role these two species could have. </jats:p>

  • 出版日期2017-4-6