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奥杜因在大鼠脑中抑制一氧化氮合酶。

Nitric oxide synthase inhibited by audouine in the rat brain.

作者信息

Asahara H, Kabuto H, Yokoi I, Habu H, Mori A, Inoue H

机构信息

Department of Orthopaedic Surgery, Okayama University Medical School, Japan.

出版信息

Neuroreport. 1995 May 30;6(8):1146-8. doi: 10.1097/00001756-199505300-00018.

Abstract

Nitric oxide synthase (NOS) synthesizes nitric oxide (NO) from L-arginine (Arg) which has a guanidino group in its molecule. Audouine, a derivative of Arg, is the diguanidino compound. In this study, the effects of audouine on rat brain NOS activity were investigated by measuring nitrite and nitrate formation. Audouine inhibited NOS activity in a competitive (Ki = 2.10 microM) and partially uncompetitive (Ki = 49.7 microM) manner. Audouine is not substituted at the guanidino nitrogen, in contrast to most previously reported NOS inhibitors which were synthesized by substituting the guanidino nitrogen of Arg. Audouine is a novel inhibitor of NOS and should be useful for investigating the chemical nature of NOS and the roles of NO in the central nervous system.

摘要

一氧化氮合酶(NOS)从分子中含有胍基的L-精氨酸(Arg)合成一氧化氮(NO)。精氨酸衍生物奥杜因是双胍基化合物。在本研究中,通过测量亚硝酸盐和硝酸盐的生成来研究奥杜因对大鼠脑NOS活性的影响。奥杜因以竞争性(Ki = 2.10 microM)和部分非竞争性(Ki = 49.7 microM)方式抑制NOS活性。与大多数先前报道的通过取代精氨酸胍基氮合成的NOS抑制剂不同,奥杜因在胍基氮处未被取代。奥杜因是一种新型的NOS抑制剂,应有助于研究NOS的化学性质以及NO在中枢神经系统中的作用。

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