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钙通道的氧化还原调控:从机制到治疗机遇

Redox control of calcium channels: from mechanisms to therapeutic opportunities.

作者信息

Hool Livia C, Corry Ben

机构信息

Discipline of Physiology, School of Biomedical, Biomolecular, and Chemical Sciences, The University of Western Australia, Crawley, Western Australia.

出版信息

Antioxid Redox Signal. 2007 Apr;9(4):409-35. doi: 10.1089/ars.2006.1446.

Abstract

Calcium plays an integral role in cellular function. It is a well-recognized second messenger necessary for signaling cellular responses, but in excessive amounts can be deleterious to function, causing cell death. The main route by which calcium enters the cytoplasm is either from the extracellular compartment or internal addistores via calcium channels. There is good evidence that calcium channels can respond to pharmacological compounds that reduce or oxidize thiol groups on the channel protein. In addition, reactive oxygen species such as hydrogen peroxide and superoxide that can mediate oxidative pathology also mediate changes in channel function via alterations of thiol groups. This review looks at the structure and function of calcium channels, the evidence that changes in cellular redox state mediate changes in channel function, and the role of redox modification of channels in disease processes. Understanding how redox modification of the channel protein alters channel structure and function is providing leads for the design of therapeutic interventions that target oxidative stress responses.

摘要

钙在细胞功能中起着不可或缺的作用。它是一种公认的第二信使,是细胞信号转导所必需的,但过量时会对功能产生有害影响,导致细胞死亡。钙进入细胞质的主要途径是通过钙通道从细胞外区室或内部储存库进入。有充分的证据表明,钙通道可对能还原或氧化通道蛋白上巯基的药理化合物作出反应。此外,诸如过氧化氢和超氧化物等能介导氧化病理过程的活性氧也通过巯基的改变介导通道功能的变化。本综述探讨了钙通道的结构和功能、细胞氧化还原状态的变化介导通道功能变化的证据,以及通道的氧化还原修饰在疾病过程中的作用。了解通道蛋白的氧化还原修饰如何改变通道结构和功能,为设计针对氧化应激反应的治疗干预措施提供了线索。

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