CEREBRAL ENDOTHELIAL NITRIC-OXIDE SYNTHASE EXPRESSION AFTER FOCAL CEREBRAL-ISCHEMIA IN RATS

被引:168
作者
ZHANG, ZG
CHOPP, M
ZALOGA, C
POLLOCK, JS
FORSTERMANN, U
机构
[1] ABBOTT LABS, ABBOTT PK, IL USA
[2] OAKLAND UNIV, DEPT PHYS, ROCHESTER, MI 48063 USA
关键词
ENDOTHELIUM; MIDDLE CEREBRAL ARTERY OCCLUSION; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; RATS;
D O I
10.1161/01.STR.24.12.2016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose. The purpose of this study was to measure the temporal profile of expression of the endothelial nitric oxide synthase (NOS) in cerebral microvessels after middle cerebral artery occlusion in the rat. Methods: Middle cerebral artery occlusion was performed on 24 male Wistar rats by extracranial insertion of a 4-0 nylon monofilament into the internal artery. Three additional rats were used as controls. Animals were killed at 1, 2, 4, 6, 24, 48, 72, and 168 hours after middle cerebral artery occlusion (n =3 per time point). Rat brains were perfused with buffer, frozen, sectioned, and stained with a monoclonal antibody against endothelial NOS. Adjacent sections were stained with hematoxylin and eosin for evaluation of neuronal damage. Results: The endothelial NOS in the cerebral vessels was upregulated at 1 hour after induction of ischemia throughout the ischemic region. The induction of the endothelial NOS progressively increased up to 24 hours of ischemia. In the periphery of the area of necrosis in the cortex, a delayed (24-hour) upregulation of the endothelial NOS remained constant throughout the duration of ischemia. Conclusions: The rapid and intense differential expression of the endothelial NOS in the core and peripheral areas of the lesion indicates a role for endothelial NOS in ischemic cell damage and suggests that the increased expression of NOS may mediate changes in the cerebral blood flow. (Stroke.
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页码:2016 / 2021
页数:6
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