Fates and vascular action of S-nitrosoglutathione and related compounds in the circulation

被引:21
作者
Kashiba, M
Kasahara, E
Chien, KC
Inoue, M
机构
[1] Natl Inst Hlth & Nutr, Div Geriatr Hlth & Nutr, Shinjuku Ku, Tokyo 1628636, Japan
[2] Osaka City Univ, Sch Med, Dept Biochem, Osaka 5458585, Japan
关键词
D O I
10.1006/abbi.1998.1055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To know the metabolism of low-molecular-weight S-nitrosothiols (RS-NO) in the circulation, we analyzed the stability and depressor effects of S-nitrosoglutathione (GS-NO) and the L- and D-forms of S-nitrosocysteine (Cys-NO). Although half-lives of these RS-NO in fresh plasma were longer than 50 min, their depressor effects disappeared within 5 min after intravenous administration of these compounds. Acivicin (AT-125), an inhibitor of gamma-glutamyltransferase (gamma-GTP), prolonged the depressor effect of OS-NO but not of Cys-NO, The depressor effect of OS-NO disappeared in AT-125-treated rats within 10 min after administration, which is still shorter than its half-life in vitro. Although S-conjugates of L-cysteine, but not of D-cysteine, rapidly enter into cells via an active transport system and disappear from the circulation, both forms of Cys-NO exhibited similar activity to decrease blood pressure to that of NO. Thus, NO might be rapidly released from Cys-NO in the circulation and shortly exhibited its depressor action. These observations suggested that the circulating OS-NO is rapidly decomposed by gamma-GTP to form Cys-NO and that the release of NO from both OS-NO and Cys-NO is enhanced significantly in the circulation. (C) 1999 Academic Press.
引用
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页码:213 / 218
页数:6
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