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内皮素-1诱导的局灶性脑缺血大鼠模型中的神经化学变化及激光多普勒血流测定

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

作者信息

Bogaert L, Scheller D, Moonen J, Sarre S, Smolders I, Ebinger G, Michotte Y

机构信息

Department of Pharmaceutical Chemistry and Drug Analysis, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.

出版信息

Brain Res. 2000 Dec 29;887(2):266-75. doi: 10.1016/s0006-8993(00)02959-0.

Abstract

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-1 (Et-1), 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-1 injected. Histological analysis of brain slices, taken from anaesthetized and conscious animals, indicated a 500 pmol dose of Et-1 was required to produce a similar infarct in anaesthetized rats to a 120 pmol dose of Et-1 in freely moving rats. The immediate drop in striatal blood flow, and the prompt increase of extracellular DA, after the micro-application of Et-1, 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.

摘要

脑缺血后,广义的神经递质向细胞外空间溢出被认为会导致随后的神经元死亡。本研究旨在通过微透析法,在局灶性短暂性脑缺血大鼠模型中,研究纹状体中神经递质多巴胺(DA)、谷氨酸(Glu)和γ-氨基丁酸(GABA)的释放情况。在自由活动的大鼠大脑中动脉(MCA)附近应用120皮摩尔内皮素-1(Et-1)诱导缺血。缺血使细胞外纹状体DA浓度大幅增加(2400%)、Glu(5500%)和GABA(800%)浓度增加。对麻醉大鼠进行激光多普勒血流仪检测表明,纹状体内血流量减少了75±11%。血流持续下降的时间与注入的Et-1浓度呈剂量依赖性关系。对麻醉和清醒动物的脑切片进行组织学分析表明,在麻醉大鼠中产生与自由活动大鼠中120皮摩尔Et-1剂量相似梗死所需的Et-1剂量为500皮摩尔。微注射Et-1后,纹状体血流量立即下降,细胞外DA迅速增加,这一点非常显著。这表明DA的释放而非Glu的溢出可能是引发最终导致细胞死亡和神经功能缺损的一系列过程的主要事件。

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