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药理学诱导的、麻醉大鼠尾状核-壳核中持续时间不足一秒的多巴胺瞬变。

Pharmacologically induced, subsecond dopamine transients in the caudate-putamen of the anesthetized rat.

作者信息

Venton B Jill, Wightman R Mark

机构信息

Department of Chemistry and Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, USA.

出版信息

Synapse. 2007 Jan;61(1):37-9. doi: 10.1002/syn.20343.

Abstract

Subsecond dopamine (DA) concentration transients have previously been observed in behaving rats. Here, we demonstrate for the first time that DA transients can be pharmacologically induced in anesthetized rats. Coadministration of the D2 receptor antagonist, haloperidol, and the DA uptake inhibitor, nomifensine, results in significantly more DA transients than either drug alone. The results show that both D2 autoreceptors and the dopamine transporter regulate subsecond DA neurotransmission.

摘要

此前在行为学实验的大鼠中已观察到亚秒级的多巴胺(DA)浓度瞬变。在此,我们首次证明在麻醉的大鼠中可通过药理学方法诱导DA瞬变。同时给予D2受体拮抗剂氟哌啶醇和DA摄取抑制剂诺米芬辛,所导致的DA瞬变显著多于单独使用任一药物时。结果表明,D2自身受体和多巴胺转运体均参与调节亚秒级的DA神经传递。

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