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2,2'-联吡啶类似物的铜配合物对鸡毒支原体NADH氧化酶和乳酸脱氢酶的抑制作用

Inhibition of NADH oxidase and lactate dehydrogenase of Mycoplasma gallisepticum by copper complexes of 2,2'-bipyridyl analogues.

作者信息

Gaisser H D, de Vries J, van der Goot H, Timmerman H

机构信息

Department of Pharmacochemistry, Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

Biochem Pharmacol. 1987 Oct 1;36(19):3237-41. doi: 10.1016/0006-2952(87)90639-3.

Abstract

In the presence of copper, 2,2'-bipyridyl analogues possess growth-inhibitory activity against Mycoplasma gallisepticum. Inhibition of the energy yielding metabolism plays a role in the mechanism of action. We showed that probably inhibition of lactate dehydrogenase and NADH oxidase is involved. Both enzymes were inhibited in vitro and in vivo by several copper 2,2'-bipyridyl complexes. A two-step mechanism of action is proposed, i.e. first a copper complex enters the cell, then after dissociation of the complex the enzymes are inhibited by free copper.

摘要

在有铜存在的情况下,2,2'-联吡啶类似物对鸡毒支原体具有生长抑制活性。能量产生代谢的抑制在其作用机制中发挥作用。我们表明,可能涉及乳酸脱氢酶和NADH氧化酶的抑制。这两种酶在体外和体内都被几种铜-2,2'-联吡啶配合物抑制。提出了一种两步作用机制,即首先铜配合物进入细胞,然后配合物解离后,酶被游离铜抑制。

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