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沙鼠进行性脑缺血期间的脑血流量与神经元损伤

Cerebral blood flow and neuronal damage during progressive cerebral ischemia in gerbils.

作者信息

Matsumoto M, Hatakeyama T, Morimoto K, Yanagihara T

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN 55905.

出版信息

Stroke. 1990 Oct;21(10):1470-7. doi: 10.1161/01.str.21.10.1470.

Abstract

A combined autoradiographic and immunohistochemical method was used to correlate the extent of focal cerebral ischemia and morphologic ischemic damage following unilateral carotid occlusion in 16 gerbils for 5-30 minutes. Immunohistochemical lesions detectable by the reaction for microtubule-associated proteins 1 and 2 were visible in the subiculum-CA1 and CA2 regions of the hippocampus and layer III/IV of the cerebral cortex after 5 minutes of ischemia (n = 4). Local blood flow was promptly reduced but still heterogeneous after 10 minutes of ischemia (n = 4); local blood flow in immunohistochemical lesions was less than 5 ml/100 g/min except in highly vulnerable regions, where flow values of 5-15 ml/100 g/min were observed. After 15 minutes of ischemia (n = 4) local blood flow in less vulnerable regions including the thalamus and caudoputamen also declined to less than 5 ml/100 g/min, and immunohistochemical lesions became visible in those regions after 30 minutes of ischemia (n = 4). On the other hand, many brain regions tolerated local blood flow of less than 5 ml/100 g/min without ischemic damage. The present study demonstrates that selective tissue vulnerability during progressive cerebral ischemia depends on the degree of hypoperfusion and on factors inherent to neurons in various brain regions.

摘要

采用放射自显影和免疫组织化学相结合的方法,对16只沙土鼠单侧颈动脉闭塞5 - 30分钟后的局灶性脑缺血范围和形态学缺血损伤进行相关性研究。缺血5分钟后(n = 4),海马体的下托 - CA1和CA2区域以及大脑皮层的III/IV层中,可通过微管相关蛋白1和2反应检测到的免疫组织化学损伤可见。缺血10分钟后(n = 4),局部血流迅速减少但仍不均匀;免疫组织化学损伤区域的局部血流低于5 ml/100 g/min,但高度易损区域除外,在这些区域观察到的血流值为5 - 15 ml/100 g/min。缺血15分钟后(n = 4),包括丘脑和尾壳核在内的较不易损区域的局部血流也降至低于5 ml/100 g/min,缺血30分钟后(n = 4),这些区域出现免疫组织化学损伤。另一方面,许多脑区能够耐受低于5 ml/100 g/min的局部血流而不发生缺血损伤。本研究表明,进行性脑缺血期间的选择性组织易损性取决于灌注不足的程度以及不同脑区神经元固有的因素。

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