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M1毒蕈碱受体刺激可降低大鼠新纹状体中天冬氨酸的释放。

M1 muscarinic receptor stimulation decreases aspartate release in the rat neostriatum.

作者信息

Expósito I, Sanz B, Mora F

机构信息

Department of Physiology, Faculty of Medicine, Complutense University of Madrid, Spain.

出版信息

Neurochem Res. 1997 Dec;22(12):1485-90. doi: 10.1023/a:1021906529055.

Abstract

This study investigates the effects of different muscarinic receptor agonists on extracellular glutamate and aspartate concentrations in the rat neostriatum. In vivo intracerebral perfusions were undertaken in the conscious rat using a concentric push-pull cannulae system. Amino acid concentrations in samples were determined by HPLC with fluorometric detection. The intrastriatal perfusion of arecoline, a M1-M2 muscarinic receptor agonist, produced a significant decrease in extracellular [ASP] (45% of decrease) but not in extracellular [GLU]. These effects were blocked by scopolamine, a M1-M2 muscarinic receptor antagonist. McN-A-343, a M1 muscarinic receptor agonist, but not the M2 muscarinic receptor agonist, oxotremorine, produced a significant decrease in extracellular [ASP] (40% of decrease) but not in extracellular [GLU]. The effects of McN-A-343 on extracellular [ASP] were blocked by pirenzepine, a M1 muscarinic receptor antagonist. These results suggest that the decrease in extracellular [ASP] could be mediated, at least in part, by M1 muscarinic receptor activation in the rat neostriatum.

摘要

本研究调查了不同毒蕈碱受体激动剂对大鼠新纹状体细胞外谷氨酸和天冬氨酸浓度的影响。采用同心推挽套管系统对清醒大鼠进行体内脑内灌注。通过高效液相色谱荧光检测法测定样品中的氨基酸浓度。M1-M2毒蕈碱受体激动剂槟榔碱纹状体内灌注使细胞外[ASP]显著降低(降低45%),但细胞外[GLU]未降低。这些效应被M1-M2毒蕈碱受体拮抗剂东莨菪碱阻断。M1毒蕈碱受体激动剂McN-A-343使细胞外[ASP]显著降低(降低40%),但细胞外[GLU]未降低,而M2毒蕈碱受体激动剂氧化震颤素则无此作用。McN-A-343对细胞外[ASP]的作用被M1毒蕈碱受体拮抗剂哌仑西平阻断。这些结果表明,细胞外[ASP]的降低至少部分可由大鼠新纹状体内M1毒蕈碱受体激活介导。

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