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放线菌素抑制脑啡肽降解酶时的复合效应。

Composite effects of actinonin when inhibiting enkephalin-degrading enzymes.

作者信息

Hachisu M, Hiranuma T, Shibazaki Y, Uotani K, Murata S, Aoyagi T, Umezawa H

出版信息

Eur J Pharmacol. 1987 May 7;137(1):59-65. doi: 10.1016/0014-2999(87)90182-8.

Abstract

Actinonin which has been found to be an inhibitor of aminopeptidase M (EC 3.4.11.2) also inhibited enkephalinase A (EC 3.4.24.11) and enkephalin aminopeptidase which were partially purified from the corpus striatum membrane of guinea-pig brain. The IC50 values were 5.6 microM for enkephalinase A and 0.39 microM for enkephalin aminopeptidase. Actinonin also inhibited with an IC50 value of 1.1 microM dipeptidyl aminopeptidase tested on whole brain homogenate of rats in the presence of thiorphan and bestatin. Analgesia was assessed by measuring the tail-flick latency of mice. The analgesic effect of [Met5]enkephalin injected intracisternally (i.cist., 50 micrograms) was potentiated by an intraperitoneal (i.p., 100 and 300 mg/kg) as well as an i.cist. (25 micrograms) injection of actinonin. Actinonin was found to inhibit all three enzymes of enkephalin metabolism and, when given peripherally, to potentiate enkephalin analgesia.

摘要

放线菌素已被发现是氨肽酶M(EC 3.4.11.2)的抑制剂,它也抑制了从豚鼠脑纹状体膜中部分纯化得到的脑啡肽酶A(EC 3.4.24.11)和脑啡肽氨肽酶。脑啡肽酶A的IC50值为5.6微摩尔,脑啡肽氨肽酶的IC50值为0.39微摩尔。在存在硫磷酰胺和贝司他汀的情况下,放线菌素对在大鼠全脑匀浆上测试的二肽基氨肽酶也有抑制作用,IC50值为1.1微摩尔。通过测量小鼠的甩尾潜伏期来评估镇痛效果。脑室内注射(i.cist.,50微克)[Met5]脑啡肽的镇痛作用,通过腹腔注射(i.p.,100和300毫克/千克)以及脑室内注射(25微克)放线菌素得到增强。发现放线菌素能抑制脑啡肽代谢的所有三种酶,并且当外周给药时,能增强脑啡肽的镇痛作用。

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