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[ADP/ATP反向转运体在环孢素A抑制线粒体内膜非特异性通透性中的作用]

[The role of the ADP/ATP-antiporter in the inhibition of nonspecific permeability of the inner mitochondrial membrane by cyclosporin A].

作者信息

Novgorodov S A, Gudz' T I, Kushnareva Iu E, Zorov D B, Kudriashov Iu B

出版信息

Biokhimiia. 1991 Mar;56(3):536-41.

PMID:1883908
Abstract

The effect of the conformational state of the ADP/ATP-antiporter on the efficiency of inhibition by cyclosporine A of the Ca(2+)-induced increase of nonspecific permeability of the inner mitochondrial membrane was under study. It was found that the ADP/ATP-antiporter inhibitor carboxyatractyloside is able to reverse the cyclosporine A-induced inhibition of this nonspecific permeability. The effect of carbocyatractyloside is manifested only in mitochondria depleted of adenine nucleotides. The bifunctional SH-reagent phenylarsine oxide is also able to reverse the cyclosporine A effect. The data obtained testify to the fact that inhibition by cyclosporine A of nonspecific permeability is due to its effect on the conformational state of the ADP/ATP-antiporter.

摘要

正在研究ADP/ATP载体的构象状态对环孢素A抑制Ca(2+)诱导的线粒体内膜非特异性通透性增加效率的影响。发现ADP/ATP载体抑制剂羧基苍术苷能够逆转环孢素A诱导的对这种非特异性通透性的抑制作用。羧基苍术苷的作用仅在缺乏腺嘌呤核苷酸的线粒体中表现出来。双功能巯基试剂苯胂氧化物也能够逆转环孢素A的作用。所获得的数据证明,环孢素A对非特异性通透性的抑制是由于其对ADP/ATP载体构象状态的影响。

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