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反复缺血在大鼠纹状体中产生的细胞外谷氨酸浓度变化。

Changes in extracellular glutamate concentration produced in the rat striatum by repeated ischemia.

作者信息

Ueda Y, Obrenovitch T P, Lok S Y, Sarna G S, Symon L

机构信息

Gough-Cooper Department of Neurological Surgery, Institute of Neurology, London, England.

出版信息

Stroke. 1992 Aug;23(8):1125-30; discussion 1131. doi: 10.1161/01.str.23.8.1125.

Abstract

BACKGROUND AND PURPOSE

Evidence suggesting that ischemia-induced neuronal damage may be linked to an extracellular overflow of glutamate has accumulated, and previous studies have shown that repetitive ischemic insults may have a cumulative effect. The purpose of this study was to investigate changes in the extracellular glutamate concentration produced by repeated brief ischemic episodes of varied severity.

METHODS

Four consecutive 3- or 5-minute periods of bilateral hemispheric ischemia were produced in rats, each ischemic period followed by 27 minutes of reperfusion. Extracellular glutamate in the striatum was monitored using microdialysis, and the electroencephalogram and extracellular direct current potential were recorded in the same tissue site to assess the severity of ischemia.

RESULTS

The results suggest that the kinetics of the increase in the extracellular glutamate concentration produced by a brief ischemic episode are similar, irrespective of whether it is a single insult or part of a repeated sequence. In all cases, the extracellular glutamate concentration increased throughout ischemia and returned to its preischemic level early during reperfusion. The pattern of changes in the ischemia-induced glutamate overflow during repetitive insults varied with the severity of ischemia, in common with the pattern of changes in the direct current potential, supporting the concept that ionic changes associated with anoxic depolarization are a major determinant of ischemia-induced glutamate overflow.

CONCLUSIONS

There may be no cumulative effect of brief repeated episodes of ischemia on the extracellular glutamate concentration, even though repeated 5-minute ischemic episodes apparently caused progressive deterioration of ionic homeostasis in some cases.

摘要

背景与目的

有证据表明,缺血诱导的神经元损伤可能与细胞外谷氨酸盐外溢有关,而且先前的研究已表明重复性缺血损伤可能具有累积效应。本研究的目的是调查由不同严重程度的反复短暂缺血发作所产生的细胞外谷氨酸盐浓度的变化。

方法

在大鼠中制造连续4次3分钟或5分钟的双侧半球缺血,每次缺血期后紧接着27分钟的再灌注。使用微透析监测纹状体内的细胞外谷氨酸盐,并在同一组织部位记录脑电图和细胞外直流电位,以评估缺血的严重程度。

结果

结果表明,短暂缺血发作所产生的细胞外谷氨酸盐浓度增加的动力学是相似的,无论其是单次损伤还是重复序列的一部分。在所有情况下,细胞外谷氨酸盐浓度在整个缺血过程中均增加,并在再灌注早期恢复到缺血前水平。重复性损伤期间缺血诱导的谷氨酸盐外溢的变化模式随缺血严重程度而变化,这与直流电位的变化模式相同,支持了与缺氧去极化相关的离子变化是缺血诱导的谷氨酸盐外溢的主要决定因素这一概念。

结论

短暂反复缺血发作对细胞外谷氨酸盐浓度可能没有累积效应,尽管在某些情况下反复5分钟缺血发作显然导致了离子稳态的逐渐恶化。

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