The reaction products of sulfide and S-nitrosoglutathione are potent vasorelaxants

• Published in: Nitric oxide Vol. 46; pp. 123 - 130
• Main Authors: Berenyiova, Andrea, Grman, Marian, Mijuskovic, Ana, Stasko, Andrej, Misak, Anton, Nagy, Peter, Ondriasova, Elena, Cacanyiova, Sona, Brezova, Vlasta, Feelisch, Martin, Ondrias, Karol
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 30.04.2015
• Subjects: Animals; Aorta - drug effects; Aorta relaxation; Electron Spin Resonance Spectroscopy; Female; Hydrogen sulfide; Male; Nitric oxide; Nitrosopersulfide; Polysulfides; Rats; Rats, Wistar; S-Nitrosoglutathione - chemistry; S-Nitrosoglutathione - metabolism; Sulfides - chemistry; Sulfides - metabolism; Uterine Contraction - drug effects; Uterus; Vasodilator Agents - chemistry; Vasodilator Agents - metabolism; Vasodilator Agents - pharmacology; Aorta relaxation; Phen; EPR; SSNO; Polysulfides; MGD; Nitrosopersulfide; GSNO; sGC; AUC; Hydrogen sulfide; NAC; ABS; AS; SNP; Uterus; cPTIO; Nitric oxide; Sn; ODQ
• ISSN: 1089-8603; 1089-8611
• DOI: 10.1016/j.niox.2014.12.008

•Products of the sulfide–GSNO interaction relax precontracted rat aortic rings.•Vasorelaxation of the reaction mixture is more pronounced and faster than with GSNO.•The reaction mixture releases NO as detected by EPR using the MGD2-Fe2+ spin trap.•Sensitivity of relaxation to thiols/metHb suggests additional involvement of HNO. The chemical interaction of sodium sulfide (Na2S) with the NO-donor S-nitrosoglutathione (GSNO) has been described to generate new reaction products, including polysulfides and nitrosopersulfide (SSNO–) via intermediacy of thionitrous acid (HSNO). The aim of the present work was to investigate the vascular effects of the longer-lived products of the Sulfide/GSNO interaction. Here we show that the products of this reaction relax precontracted isolated rings of rat thoracic aorta and mesenteric artery (but to a lesser degree rat uterus) with a >2-fold potency compared with the starting material, GSNO (50 nM), whereas Na2S and polysulfides have little effect at 1–5 µM. The onset of vasorelaxation of the reaction products was 7–10 times faster in aorta and mesenteric arteries compared with GSNO. Relaxation to GSNO (100–500 nM) was blocked by an inhibitor of soluble guanylyl cyclase, ODQ (0.1 and 10 µM), and by the NO scavenger cPTIO (100 µM), but less affected by prior acidification (pH 2–4), and unaffected by N-acetylcysteine (1 mM) or methemoglobin (20 µM heme). By contrast, relaxation to the Sulfide/GSNO reaction products (100–500 nM based on the starting material) was inhibited to a lesser extent by ODQ, only slightly decreased by cPTIO, more markedly inhibited by methemoglobin and N-acetylcysteine, and abolished by acidification before addition to the organ bath. The reaction mixture was found to generate NO as detected by EPR spectroscopy using N-(dithiocarboxy)-N-methyl-D-glucamine (MGD2)-Fe2+ as spin trap. In conclusion, the Sufide/GSNO reaction products are faster and more pronounced vasorelaxants than GSNO itself. We conclude that in addition to NO formation from SSNO–, reaction products other than polysulfides may give rise to nitroxyl (HNO) and be involved in the pronounced relaxation induced by the Sulfide/GSNO cross-talk.