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前列腺素E1、E2、F2α和花生四烯酸对雄性大鼠肠道和肝脏微粒体芳烃羟化酶活性的影响。

Effects of prostaglandins E1, E2, F2 alpha and arachidonic acid on aryl hydrocarbon hydroxylase activity of intestinal and hepatic microsomes from male rats.

作者信息

Stohs S J, Wu L J

出版信息

Res Commun Chem Pathol Pharmacol. 1981 Dec;34(3):461-71.

PMID:6798653
Abstract

The in vitro effects of prostaglandins E1, E2, F2 alpha and arachidonic acid on microsomal aryl hydrocarbon hydroxylase (AHH) activity from rat liver and intestinal mucosa were examined. PGE1 and PGE2 stimulated AHH activity of intestinal microsomes, while both prostaglandins had an inhibitory effect on AHH activity of liver microsomes. PGF2 alpha had little effect on AHH activity of intestinal and hepatic microsomes. Arachidonic acid exerted strongly inhibitory effects on AHH activity of both intestine and liver, with the greatest inhibition being exerted against intestinal AHH. Kinetic studies demonstrated that the inhibition of hepatic AHH activity by PGE1 at concentrations of 0.10 mM or less was non-competitive.

摘要

研究了前列腺素E1、E2、F2α和花生四烯酸对大鼠肝脏和肠黏膜微粒体芳烃羟化酶(AHH)活性的体外作用。前列腺素E1和E2刺激肠微粒体的AHH活性,而这两种前列腺素对肝微粒体的AHH活性均有抑制作用。前列腺素F2α对肠和肝微粒体的AHH活性影响很小。花生四烯酸对肠和肝的AHH活性均有强烈抑制作用,对肠AHH的抑制作用最强。动力学研究表明,浓度为0.10 mM或更低时,前列腺素E1对肝AHH活性的抑制作用是非竞争性的。

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