Suppr超能文献

内源性兴奋性氨基酸对伏隔核中多巴胺释放的不同作用。

Distinct actions of endogenous excitatory amino acids on the outflow of dopamine in the nucleus accumbens.

作者信息

Youngren K D, Daly D A, Moghaddam B

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut.

出版信息

J Pharmacol Exp Ther. 1993 Jan;264(1):289-93.

PMID:8093728
Abstract

Intracerebral microdialysis was utilized to assess the effect of endogenous excitatory amino acids (EAA), l-glutamate (GLU) and l-aspartate (ASP), on the extracellular levels of dopamine in the rat nucleus accumbens. Both ASP and GLU produced a release response at a concentration range of 1 to 10 mM. GLU was generally less efficacious in increasing dopamine outflow; at 5 and 10 mM, the maximum effect exerted by GLU was significantly less than that observed with ASP. The specific N-methyl-D-aspartate (NMDA) antagonist 2-amino-5-phosphonopentanoic (AP5) acid was more effective in attenuating the actions of 5 and 10 mM ASP than the non-NMDA antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX). On the other hand, the stimulatory actions of 5 and 10 mM GLU were more effectively decreased with CNQX when compared with AP5. Perfusion of tetrodotoxin before application of either GLU or ASP blocked the excitatory effect of these amino acids on dopamine overflow. These results suggest that in the nucleus accumbens, ASP and GLU may increase dopamine release through distinct mechanisms and that their stimulatory action is dependent on axonal impulse flow.

摘要

采用脑内微透析技术评估内源性兴奋性氨基酸(EAA)、L-谷氨酸(GLU)和L-天冬氨酸(ASP)对大鼠伏隔核细胞外多巴胺水平的影响。ASP和GLU在1至10 mM的浓度范围内均产生释放反应。GLU在增加多巴胺外流方面通常效果较差;在5和10 mM时,GLU产生的最大效应明显小于ASP所观察到的效应。特异性N-甲基-D-天冬氨酸(NMDA)拮抗剂2-氨基-5-膦酰基戊酸(AP5)在减弱5和10 mM ASP的作用方面比非NMDA拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)更有效。另一方面,与AP5相比,CNQX能更有效地降低5和10 mM GLU的刺激作用。在应用GLU或ASP之前灌注河豚毒素可阻断这些氨基酸对多巴胺溢出的兴奋作用。这些结果表明,在伏隔核中,ASP和GLU可能通过不同机制增加多巴胺释放,且它们的刺激作用依赖于轴突冲动流。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验