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甘氨酸逆转乙醇诱导的对N-甲基-D-天冬氨酸刺激的神经递质释放的抑制作用中的脑区差异。

Brain regional differences in glycine reversal of ethanol-induced inhibition of N-methyl-D-aspartate-stimulated neurotransmitter release.

作者信息

Gonzales R A, Brown L M

机构信息

Institute for Neuroscience, College of Pharmacy, University of Texas, Austin 78712.

出版信息

Life Sci. 1995;56(8):571-7. doi: 10.1016/0024-3205(94)00489-f.

Abstract

The present study investigated the interaction between glycine and ethanol on N-methyl-D-aspartate (NMDA)-stimulated neurotransmitter release in hippocampal, cerebrocortical, and striatal slices from rat brain. Some, but not all, previous studies have shown that glycine may reverse the inhibitory effect of ethanol on NMDA receptors. Hippocampal or cortical slices were prepared and prelabelled with [3H]norepinephrine, and striatal slices were labelled with [3H]dopamine. Stimulation of the slices with 500 microM NMDA for two minutes caused a significant release of [3H]neurotransmitter in each brain region above basal. Ethanol (60 mM) significantly inhibited the NMDA-stimulated release of neurotransmitter from all brain regions. Addition of glycine (0.3-3 microM) to the buffer bathing the slices had no effect on the inhibitory effect of ethanol in hippocampus or cortex. However, in striatal slices, 0.3 and 1.0 microM glycine added to the buffer reversed the inhibitory effect of ethanol on NMDA-stimulated [3H]dopamine release without having any effect on either basal or NMDA-stimulated release by itself. These results show that the interaction between ethanol and glycine varies in different brain regions. Therefore interpretation of the potential inhibitory effect of ethanol on NMDA receptor function in vivo should consider brain region and local concentrations of glycine.

摘要

本研究调查了甘氨酸与乙醇对大鼠脑海马、大脑皮质及纹状体切片中N-甲基-D-天冬氨酸(NMDA)刺激的神经递质释放的相互作用。一些(但并非全部)先前的研究表明,甘氨酸可能会逆转乙醇对NMDA受体的抑制作用。制备海马或皮质切片并用[3H]去甲肾上腺素进行预标记,纹状体切片用[3H]多巴胺进行标记。用500微摩尔/升NMDA刺激切片两分钟,导致每个脑区中[3H]神经递质的释放量显著高于基础水平。乙醇(60毫摩尔/升)显著抑制了所有脑区中NMDA刺激的神经递质释放。向浸泡切片的缓冲液中添加甘氨酸(0.3 - 3微摩尔/升)对乙醇在海马或皮质中的抑制作用没有影响。然而,在纹状体切片中,向缓冲液中添加0.3和1.0微摩尔/升的甘氨酸可逆转乙醇对NMDA刺激的[3H]多巴胺释放的抑制作用,而其本身对基础或NMDA刺激的释放均无影响。这些结果表明,乙醇与甘氨酸之间的相互作用在不同脑区有所不同。因此,在体内解释乙醇对NMDA受体功能的潜在抑制作用时,应考虑脑区和甘氨酸的局部浓度。

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