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脑啡肽降解抑制剂对离体豚鼠回肠的作用。

Effect of inhibitors of enkephalin degradation in the isolated guinea-pig ileum.

作者信息

van Amsterdam J G, van Buuren K J, Krielaart M J, Zuiderveld O P, Tijms R P

机构信息

Department of Pharmacy, University of Amsterdam, The Netherlands.

出版信息

Life Sci. 1988;43(19):1529-36. doi: 10.1016/0024-3205(88)90401-8.

Abstract

Bestatin and high concentration of puromycin increase the depressing effect of [Met] enkephalin on the twitch response of the electrically stimulated guinea-pig ileum. Thiorphan (enkephalinase A inhibitor) is hardly effective, but phelorphan (mercapto-acetyl-Phe-Phe) a newly synthesized enzyme-inhibitor which effectively inhibits the enkephalinase A, enkephalinase B and soluble aminopeptidase activity, potentiates the effect of enkephalin dose-dependently and in low concentrations (0.01-1 microM). Enkephalinase A, though present in these tissues, is not functional under the conditions of the test, because it is inhibited by the physiological buffer itself. These results demonstrate that enkephalinase B and the membrane bound aminopeptidase, but not the soluble aminopeptidase or enkephalinase A hydrolyse enkephalins in the isolated guinea-pig ileum.

摘要

贝抑素和高浓度的嘌呤霉素增强了[甲硫]脑啡肽对电刺激豚鼠回肠抽搐反应的抑制作用。硫醇苯丙氨酸(脑啡肽酶A抑制剂)几乎无效,但苯丙氨酸(巯基乙酰 - 苯丙氨酸 - 苯丙氨酸)是一种新合成的酶抑制剂,可有效抑制脑啡肽酶A、脑啡肽酶B和可溶性氨肽酶的活性,在低浓度(0.01 - 1微摩尔)时剂量依赖性地增强脑啡肽的作用。脑啡肽酶A虽然存在于这些组织中,但在测试条件下不起作用,因为它被生理缓冲液本身抑制。这些结果表明,在离体豚鼠回肠中,脑啡肽酶B和膜结合氨肽酶可水解脑啡肽,而可溶性氨肽酶或脑啡肽酶A则不能。

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