线粒体H+泄漏与产热。

IF 15.7 1区 医学 Q1 PHYSIOLOGY
Ambre M Bertholet, Yuriy Kirichok
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引用次数: 19

摘要

所有组织的线粒体都将各种代谢底物转化为两种形式的能量:ATP和热量。历史上,线粒体生物能量学研究的主要焦点是ATP产生的机制,而线粒体产热受到的关注明显较少。然而,线粒体产热对于维持体温、调节代谢速度以及防止线粒体和细胞的氧化损伤至关重要。此外,线粒体产热作为治疗代谢紊乱的药理靶点也具有重要意义。线粒体产生热量是由于H+渗漏穿过它们的内膜。本文综述了线粒体H+泄漏和产热的最新研究进展,重点关注了介导线粒体H+泄漏的两种蛋白解偶联蛋白1和ADP/ATP载体的功能和调控的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mitochondrial H<sup>+</sup> Leak and Thermogenesis.

Mitochondrial H<sup>+</sup> Leak and Thermogenesis.

Mitochondrial H<sup>+</sup> Leak and Thermogenesis.

Mitochondrial H+ Leak and Thermogenesis.

Mitochondria of all tissues convert various metabolic substrates into two forms of energy: ATP and heat. Historically, the primary focus of research in mitochondrial bioenergetics was on the mechanisms of ATP production, while mitochondrial thermogenesis received significantly less attention. Nevertheless, mitochondrial heat production is crucial for the maintenance of body temperature, regulation of the pace of metabolism, and prevention of oxidative damage to mitochondria and the cell. In addition, mitochondrial thermogenesis has gained significance as a pharmacological target for treating metabolic disorders. Mitochondria produce heat as the result of H+ leak across their inner membrane. This review provides a critical assessment of the current field of mitochondrial H+ leak and thermogenesis, with a focus on the molecular mechanisms involved in the function and regulation of uncoupling protein 1 and the ADP/ATP carrier, the two proteins that mediate mitochondrial H+ leak.

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来源期刊
Annual review of physiology
Annual review of physiology 医学-生理学
CiteScore
35.60
自引率
0.00%
发文量
41
期刊介绍: Since 1939, the Annual Review of Physiology has been highlighting significant developments in animal physiology. The journal covers diverse areas, including cardiovascular physiology, cell physiology, ecological, evolutionary, and comparative physiology, endocrinology, gastrointestinal physiology, neurophysiology, renal and electrolyte physiology, respiratory physiology, and special topics.
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