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

机译:内皮素-1大鼠局灶性脑缺血模型的神经化学变化和激光多普勒血流仪。

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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.
机译:脑缺血后,广泛的神经递质溢出到细胞外空间,已被认为可导致随后的神经元死亡。这项研究的目的是在局部局灶性脑缺血的大鼠模型中通过微透析研究神经递质多巴胺(DA),谷氨酸(Glu)和γ-氨基丁酸(GABA)的纹状体释放。在活动自由的大鼠中,通过在靠近大脑中动脉(MCA)处应用120 pmol内皮素-1(Et-1)诱导缺血。缺血导致细胞外纹状体DA浓度(2400%),Glu(5500%)和GABA(800%)浓度大幅增加。麻醉大鼠的激光多普勒血流仪显示,纹状体内的血流减少了75 +/- 11%。血流持续下降的时间与剂量Et-1剂量相关。取自麻醉和清醒动物的脑切片的组织学分析表明,要在麻醉大鼠中产生与自由活动大鼠中120 pmol剂量的Et-1类似的梗塞,需要500 pmol剂量的Et-1。微量施用Et-1后,纹状体血流量立即下降,细胞外DA迅速增加,这是非常惊人的。这表明DA释放而不是Glu溢出可能是引发级联反应的主要事件,最终导致细胞死亡和神经功能缺损。

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