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单胺氧化酶B对一组强效抑制剂的敏感性存在显著的物种差异。

Dramatic species differences in the susceptibility of monoamine oxidase B to a group of powerful inhibitors.

作者信息

Krueger M J, Mazouz F, Ramsay R R, Milcent R, Singer T P

机构信息

Department of Biochemistry and Biophysics, University of California at San Francisco 94143.

出版信息

Biochem Biophys Res Commun. 1995 Jan 17;206(2):556-62. doi: 10.1006/bbrc.1995.1079.

Abstract

Oxadiazolones and oxadiazolethiones are potent, reversible competitive inhibitors of MAO B in rat brain mitochondria. We have compared the Ki values of six of these inhibitors towards MAO B from rat, human and beef liver mitochondria, using benzylamine as substrate. Unexpectedly, their inhibitory potency varies by 3 to 4 orders of magnitude between rat and beef liver MAO B, whereas the inhibition of the rat and human liver enzymes is quite similar. Examples are 5-(4-benzyl-oxyphenyl)-3-(2-cyano-ethyl)-1,3,4-oxadiazole-2(3H)-th ione, with Ki at 30 degrees of 0.5 nM for rat, 0.8 nM for human, and 1,830 nM for beef liver mitochondria and 5-(4-benzyloxyphenyl)-3-(2-hydroxyethyl)-1,3,4-oxadiazol-2(3 H)-one with Ki values of 1.2, 1.1 and 1,320 nM for MAO B from these three sources. Since solubilized and membrane-bound enzymes had similar sensitivities to the inhibitors, the differences seen must arise from differences in the amino acid sequences of the three enzymes.

摘要

恶二唑酮和恶二唑硫酮是大鼠脑线粒体中MAO B的强效、可逆竞争性抑制剂。我们以苄胺为底物,比较了其中六种抑制剂对大鼠、人及牛肝线粒体中MAO B的Ki值。出乎意料的是,它们对大鼠和牛肝MAO B的抑制效力相差3至4个数量级,而对大鼠和人肝酶的抑制作用相当相似。例如,5-(4-苄氧基苯基)-3-(2-氰基乙基)-1,3,4-恶二唑-2(3H)-硫酮,在30℃时对大鼠MAO B的Ki为0.5 nM,对人MAO B的Ki为0.8 nM,对牛肝线粒体MAO B的Ki为1830 nM;以及5-(4-苄氧基苯基)-3-(2-羟乙基)-1,3,4-恶二唑-2(3H)-酮,对这三种来源的MAO B的Ki值分别为1.2、1.1和1320 nM。由于溶解的酶和膜结合酶对抑制剂的敏感性相似,观察到的差异必定源于这三种酶氨基酸序列的不同。

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