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KMID : 0380219930260050391
Journal of Biochemistry and Molecular Biology
1993 Volume.26 No. 5 p.391 ~ p.395
Transnitrosation as a Predominant Mechanism in the Hypotensive Effect of S-Nitrosothiols
Jeen-Woo Park
Abstract
S-Nitrosothiols, which are possible intermediates in the pharmacological mechanisms of many vasodilators, undergo homolysis at pH 7.4 and 37¡£C to give corresponding disulfides and nitric oxide. At normal dosages, this reaction is
too
slow to be an obligatory step in the pharmacological mechanisms of these usually fast-acting drugs. Transfers of the nitroso moiety of S-nitrosothiols to acceptors such as thiols or certain hemeproteins are much faster. The highly unstable
S-nitrosothiols such S-nitosothiols such as S-nitrosocysteine and S-nitroso-N-acetyl-DL-peniicillamine and the relatively stable S-nitrosothiols such as S-nitrosoglutathione and S-nitrosocaptopril had similar
effects
on guanylate cyclase activation as well as on the transfer of niric oxide to hemoglobin. These findings suggest that S-nitrosothiols could act as a hypotensive agent via the transfer of nitric oxide to the heme moiety of guanylate cyclase.
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