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海马多巴胺受体调节腹侧海马化学刺激诱发的大鼠伏隔核中cFos的表达。

Hippocampal dopamine receptors modulate cFos expression in the rat nucleus accumbens evoked by chemical stimulation of the ventral hippocampus.

作者信息

Zornoza Teodoro, Cano-Cebrián María J, Martínez-García Fernando, Polache Ana, Granero Luis

机构信息

Department de Farmàcia i Tecnología Farmacèutica, Facultat de Farmàcia, Universitat de València, Avda Vicente Andres Estelles s/n, 46100 Burjassot, Valencia, Spain.

出版信息

Neuropharmacology. 2005 Dec;49(7):1067-76. doi: 10.1016/j.neuropharm.2005.06.005. Epub 2005 Jul 22.

DOI:10.1016/j.neuropharm.2005.06.005
PMID:16040065
Abstract

Recently, we have shown that D1 and D2 receptors in the ventral hippocampus (VH) modulate both the locomotor activation and the increase in dopamine (DA) levels in the rat nucleus accumbens (NAc) induced by NMDA stimulation of the VH. In the present study we analyze the possible role of VH D1 and D2 receptors in the modulation of the cFos expression in NAc (core and shell subregions) and in dorsal striatum. This was assessed by immunohistochemical analysis of cFos expression in the rat brains after retro-dialysis application of NMDA (50mM, 10 min) into VH, in absence and in presence of either the D1/D5 receptor antagonist SCH 23390 (100 and 250 microM, 60 min) or the D2 receptor antagonist raclopride (100 and 250 microM, 60 min). NMDA induced a robust increase in the cFos expression in the NAc shell, both in the ipsilateral and contralateral side. No statistically significant increases were observed in the NAc core and in the dorsal striatum. Simultaneous application of SCH 23390 and NMDA into the VH attenuated the NMDA-evoked cFos expression in NAc shell. In contrast, raclopride had no significant effect. Our present results show that the NMDA receptor mediated effects in the VH require D1 receptors and suggest that DA in VH strongly modulates the excitatory outputs from this brain area.

摘要

最近,我们发现腹侧海马(VH)中的D1和D2受体可调节由VH的NMDA刺激诱导的大鼠伏隔核(NAc)中的运动激活以及多巴胺(DA)水平的升高。在本研究中,我们分析了VH D1和D2受体在调节NAc(核心和壳亚区)和背侧纹状体中cFos表达方面的可能作用。这是通过在不存在和存在D1/D5受体拮抗剂SCH 23390(100和250微摩尔,60分钟)或D2受体拮抗剂雷氯必利(100和250微摩尔,60分钟)的情况下,将NMDA(50毫摩尔,10分钟)逆行透析应用于VH后,对大鼠大脑中cFos表达进行免疫组织化学分析来评估的。NMDA诱导了NAc壳同侧和对侧cFos表达的强烈增加。在NAc核心和背侧纹状体中未观察到统计学上的显著增加。将SCH 23390和NMDA同时应用于VH可减弱NMDA诱发的NAc壳中的cFos表达。相比之下,雷氯必利没有显著影响。我们目前的结果表明,VH中NMDA受体介导的效应需要D1受体,并表明VH中的DA强烈调节该脑区的兴奋性输出。

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