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[ADP/ATP 反向转运体在肝脏线粒体脂肪酸解偶联作用中的参与]

[Participation of the ADP/ATP-antiporter in the uncoupling action of fatty acids in liver mitochondria].

作者信息

Bodrova M E, Markova O V, Mokhova E N, Samartsev V N

出版信息

Biokhimiia. 1995 Aug;60(8):1349-57.

PMID:7578587
Abstract

The controversial data on the involvement of the ATP/ADP-antiporter in the uncoupling effect of fatty acids in liver mitochondria as well as on the sensitivity of the uncoupling process to the ATP/ADP-antiporter inhibitor, carboxyatractylate, have been analyzed. It has been shown that in liver mitochondria uncoupled by palmitic acid, pyridoxal-5-phosphate, diethyl pyrocarbonate and glutamate produce an additional recoupling action against the background of carboxyatractylate. No such effect is observed during mitochondrial uncoupling by FCCP. Micromolar concentrations of ADP added prior to palmitic acid produce a far more potent coupling action; the subsequent recoupling effect of carboxyatractylate diminishes thereby. This finding suggests that the reduction of endogenous ADP is responsible for the increased sensitivity of the uncoupling action of fatty acids to carboxyatractylate. It is concluded that the ATP/ADP-antiporter and other membrane carriers play a role in the uncoupling action of fatty acids on liver mitochondria.

摘要

关于ATP/ADP反向转运体参与脂肪酸对肝线粒体解偶联作用以及解偶联过程对ATP/ADP反向转运体抑制剂羧基苍术苷敏感性的争议性数据已得到分析。结果表明,在由棕榈酸解偶联的肝线粒体中,磷酸吡哆醛、焦碳酸二乙酯和谷氨酸在羧基苍术苷存在的背景下产生额外的再偶联作用。在用FCCP使线粒体解偶联的过程中未观察到这种效应。在棕榈酸之前加入微摩尔浓度的ADP会产生更强的偶联作用;羧基苍术苷随后的再偶联效应因此减弱。这一发现表明,内源性ADP的减少是脂肪酸解偶联作用对羧基苍术苷敏感性增加的原因。结论是,ATP/ADP反向转运体和其他膜载体在脂肪酸对肝线粒体的解偶联作用中起作用。

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