NITROGLYCERIN METABOLISM IN VASCULAR TISSUE - ROLE OF GLUTATHIONE S-TRANSFERASES AND RELATIONSHIP BETWEEN NO. AND NO2- FORMATION

被引:79
作者
KURZ, MA
BOYER, TD
WHALEN, R
PETERSON, TE
HARRISON, DG
机构
[1] EMORY UNIV,SCH MED,DEPT INTERNAL MED,ATLANTA,GA 30322
[2] VET ADM MED CTR,ATLANTA,GA 30033
关键词
D O I
10.1042/bj2920545
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
Nitroglycerin is a commonly employed pharmacological agent which produces vasodilatation by release of nitric oxide (NO.). the mechanism by which nitroglycerin releases NO. remains undefined. Recently, glutathione S-transferases have been implicated as important contributors to this process. They are known to release NO2- from nitroglycerin, but have not been shown to release NO2. The present studies were designed to examine the role of endogenous glutathione S-transferases in this metabolic process. Homogenates of dog carotid artery were incubated anaerobically with nitroglycerin, and NO. and NO2- production was determined by chemiluminescence. The role of glutathione S-transferases was studied by incubating homogenates with nitroglycerin in the presence of 1 mM GSH or 1 mM S-hexylglutathione, a potent inhibitor of glutathione S-transferases. Homogenates released 163 pmol of NO./h per mg of protein from nitroglycerin, and 2370 pmol of NO2-/h per mg. Adding GSH decreased NO. production by 82 % and increased NO2-production by 98 %. S-Hexylglutathione-inhibited glutathione S-transferase activity by 96 % and decreased NO2- production by 78 % but had no effect on NO. release. A linear relationship between glutathione S-transferase activity and NO2- production was observed, whereas glutathione S-transferase activity and NO' release were unrelated. Western-blot analysis demonstrated that dog carotid vascular smooth muscle contained Pi and Mu forms of glutathione S-transferases, with a predominance of the former. Purified preparations of human Pi and rat Mu isoforms metabolized nitroglycerin only to NO2- and not to NO.. On the basis of these findings, we conclude that (1) glutathione S-transferases do not contribute to the bioconversion of nitroglycerin to NO., but instead act as a degradative pathway for nitroglycerin, and (2) the release of NO. from nitroglycerin is not dependent on the formation of NO2-.
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页码:545 / 550
页数:6
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