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腹侧被盖区的兴奋性氨基酸受体调节腹侧纹状体中的多巴胺释放。

Excitatory amino acid receptors in the ventral tegmental area regulate dopamine release in the ventral striatum.

作者信息

Karreman M, Westerink B H, Moghaddam B

机构信息

Department of Psychiatry, Yale University School of Medicine, West Haven, Connecticut 06516, USA.

出版信息

J Neurochem. 1996 Aug;67(2):601-7. doi: 10.1046/j.1471-4159.1996.67020601.x.

DOI:10.1046/j.1471-4159.1996.67020601.x
PMID:8764585
Abstract

The role of excitatory amino acid (EAA) receptors located in the ventral tegmental area (VTA) in tonic and phasic regulation of dopamine release in the ventral striatum was investigated. Microdialysis in conscious rats was used to assess dopamine release primarily from the nucleus accumbens shell region of the ventral striatum while applying EAA antagonists or agonists to the VTA. Infusion of the AMPA/kainate receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (25 and 100 microM) into the VTA did not affect dopamine release in the ventral striatum. In contrast, intra-VTA infusion of the NMDA receptor antagonist 2-amino-5-phosphopentanoic acid (100 and 500 microM) dose-dependently decreased the striatal release of dopamine. Intra-VTA application of the ionotropic EAA receptor agonists NMDA and AMPA dose-dependently (10 and 100 microM) increased dopamine efflux in the ventral striatum. However, infusion of 50 or 500 microM trans-(+/-)-1-amino-1,3-cyclopentanedicarboxylic acid (ACPD), a metabotropic EAA receptor agonist, did not significantly affect these levels. These data suggest that NMDA receptors in the VTA exert a tonic excitatory influence on dopamine release in the ventral striatum. Furthermore, dopamine neurotransmission in this region may be enhanced by activation of NMDA and AMPA receptors, but not ACPD-sensitive metabotropic receptors, located in the VTA. These data further suggest that EAA regulation of dopamine release primarily occurs in the VTA as opposed to presynaptically at the terminal level.

摘要

研究了位于腹侧被盖区(VTA)的兴奋性氨基酸(EAA)受体在腹侧纹状体多巴胺释放的紧张性和相位性调节中的作用。在清醒大鼠中进行微透析,在向VTA应用EAA拮抗剂或激动剂的同时,主要评估腹侧纹状体伏隔核壳区的多巴胺释放。向VTA注入AMPA/海人酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(25和100微摩尔)不影响腹侧纹状体中的多巴胺释放。相反,向VTA内注入NMDA受体拮抗剂2-氨基-5-磷酸戊酸(100和500微摩尔)剂量依赖性地降低了纹状体中多巴胺的释放。向VTA内应用离子型EAA受体激动剂NMDA和AMPA剂量依赖性地(10和100微摩尔)增加了腹侧纹状体中的多巴胺流出。然而,注入50或500微摩尔反式-(±)-1-氨基-1,3-环戊烷二羧酸(ACPD),一种代谢型EAA受体激动剂,并未显著影响这些水平。这些数据表明,VTA中的NMDA受体对腹侧纹状体中的多巴胺释放施加紧张性兴奋影响。此外,该区域的多巴胺神经传递可能通过激活位于VTA中的NMDA和AMPA受体而增强,但不是通过ACPD敏感的代谢型受体。这些数据进一步表明,EAA对多巴胺释放的调节主要发生在VTA,而不是在突触前的终末水平。

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