The Biochemistry and Physiology of S-Nitrosothiols
- 1 April 2002
- journal article
- review article
- Published by Annual Reviews in Annual Review of Pharmacology and Toxicology
- Vol. 42 (1) , 585-600
- https://doi.org/10.1146/annurev.pharmtox.42.092501.104328
Abstract
S-nitrosothiols are biological metabolites of nitric oxide. It has often been suggested that they represent a more stable metabolite of nitric oxide that can either be stored, or transported, although the evidence for this is sparse. There are many unanswered questions concerning how S-nitrosothiols are formed, how they are metabolized and how they elicit biological responses. These questions are highlighted by the fact that the known chemistry of nitric oxide, thiols, and S-nitrosothiols cannot serve to explain their proposed biological activities. This review attempts to highlight the gulf between our chemical understanding of S-nitrosothiols and the proposed biological activities of these compounds with respect to guanylyl cyclase-independent nitric oxide bioactivity and also the control of vascular tone.Keywords
This publication has 80 references indexed in Scilit:
- Role of Mitogen-Activated Protein Kinases inS-Nitrosoglutathione-Induced Macrophage ApoptosisBiochemistry, 1999
- Inhibition of Clotting Factor XIII Activity by Nitric OxideBiochemical and Biophysical Research Communications, 1998
- Nitric Oxide Reversibly Inhibits Seven Members of the Caspase Family via S-NitrosylationBiochemical and Biophysical Research Communications, 1997
- Inhibition of creatine kinase by S‐nitrosoglutathioneFEBS Letters, 1996
- Albumin Is an Important Vascular Tonus Regulator as a Reservoir of Nitric OxideBiochemical and Biophysical Research Communications, 1996
- Role of ascorbic acid in the metabolism of S‐nitroso‐glutathioneFEBS Letters, 1996
- Photosensitized decomposition of S‐nitrosothiols and 2‐methyl‐2‐nitrosopropane Possible use for site‐directed nitric oxide productionFEBS Letters, 1995
- Reaction of nitric oxide with hydrogen peroxide to produce potentially cytotoxic singlet oxygen as a model for nitric oxide‐mediated killingFEBS Letters, 1993
- Guanylate cyclase activation by nitroprusside and nitrosoguanidine is related to formation of S-nitrosothiol intermediatesBiochemical and Biophysical Research Communications, 1980
- Possible involvement of S‐nitrosothiols in the activation of guanylate cyclase by nitroso compoundsFEBS Letters, 1980