Neurochemical changes and laser Doppler flowmetry in the endothelin-1 rat model for focal cerebral ischemia

被引:67
作者
Bogaert, L
Scheller, D
Moonen, J
Sarre, S
Smolders, I
Ebinger, G
Michotte, Y
机构
[1] Free Univ Brussels, Dept Pharmaceut Chem & Drug Anal, B-1090 Brussels, Belgium
[2] Free Univ Brussels, Dept Neurol, B-1090 Brussels, Belgium
[3] Janssen Cilag GmbH, Drug Discovery, D-41470 Neuss, Germany
关键词
monitoring focal cerebral ischemia; endothelin-1; microdialysis; laser Doppler flowmetry; neurotransmitters;
D O I
10.1016/S0006-8993(00)02959-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Generalized neurotransmitter overflow into the extracellular space, after cerebral ischemia, has been suggested to contribute to subsequent neuronal death. This study aims to investigate the striatal release of the neurotransmitters dopamine (DA), glutamate (Glu) and gamma-aminobutyric acid (GABA) by means of microdialysis, in a rat model for focal transient cerebral ischemia. Ischemia was induced by the application of 120 pmol endothelin-l (Et-l). adjacent to the middle cerebral artery (MCA) in freely moving rats. Ischemia produced a large increase in extracellular striatal DA concentrations (2400%), Glu (5500%) and GABA (800%) concentrations. Laser Doppler flowmetry in anaesthetized rats, indicated that the blood flow within the striatum decreased by 75+/-11%. The period of sustained drop of blood flow, was dose-dependently related to the concentration Et-l injected. Histological analysis of brain slices, taken from anaesthetized and conscious animals, indicated a 500 pmol dose of Et-l was required to produce a similar infarct in anaesthetized rats to a 120 pmol: dose of Et-l in freely moving rats. The immediate drop in striatal blood flow, and the prompt increase of extracellular DA, after the micro-application of Et-l, were quite striking. This suggests that the DA release, rather than the Glu overflow may be the primary event initiating the cascade of processes ultimately leading to cell death and neurological deficits. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:266 / 275
页数:10
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