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缺氧和缺血期间神经元中的钙和pH稳态。

Calcium and pH homeostasis in neurons during hypoxia and ischemia.

作者信息

Yao Hang, Haddad Gabriel G

机构信息

Department of Pediatrics, Kennedy Center, Albert Einstein College of Medicine, Children's Hospital at Montefiore, 1410 Pelham Parkway South, Bronx, NY 10461, USA.

出版信息

Cell Calcium. 2004 Sep-Oct;36(3-4):247-55. doi: 10.1016/j.ceca.2004.02.013.

Abstract

One of the important events during hypoxia or ischemia in the brain (or other organs for that matter, including the myocardium) is the accumulation of Ca2+ ions intracellularly. Although various studies have shown various sources of and routes for Ca2+ entry and accumulation, it is clear now that it is likely that there is a multitude rather than a single mechanism for this accumulation. In this review, we highlight this Ca2+ accumulation during low O2 states and discuss some of the mechanisms leading to accumulation for two main reasons: (a) an accumulation of Ca2+ in the cytosol has been proven to be deleterious for cell function although this accumulation of Ca2+ and consequences represent only a limited view of events that can lead to cell injury during such stress and (b) developing therapeutic strategies involving the reduction or elimination of this accumulation depends, by and large, on the mechanism of entry. In addition to reviewing some of these Ca2+ events, we will also review the relation between pH (H+) and Ca2+ since these two ions and their regulation are tied to each other in a major way. For example, extracellular acidosis, which can occur during ischemia, has a remarkable effect on the function of some of the Ca2+ entry routes.

摘要

大脑(或其他器官,包括心肌)在缺氧或缺血期间的一个重要事件是细胞内Ca2+离子的积累。尽管各种研究已经揭示了Ca2+进入和积累的多种来源及途径,但现在很清楚的是,这种积累可能存在多种机制,而非单一机制。在这篇综述中,我们着重阐述低氧状态下的这种Ca2+积累,并讨论导致积累的一些机制,主要有两个原因:(a)已证明细胞质中Ca2+的积累对细胞功能有害,尽管这种Ca2+积累及其后果只是导致此类应激期间细胞损伤的众多事件中的有限部分;(b)开发减少或消除这种积累的治疗策略在很大程度上取决于Ca2+进入的机制。除了回顾其中一些Ca2+相关事件外,我们还将回顾pH(H+)与Ca2+之间的关系,因为这两种离子及其调节在很大程度上相互关联。例如,缺血期间可能发生的细胞外酸中毒对某些Ca2+进入途径的功能有显著影响。

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