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前脑和脑干胆碱能回路对多巴胺能活动和探索性运动行为的相反调节作用。

Opposing regulation of dopaminergic activity and exploratory motor behavior by forebrain and brainstem cholinergic circuits.

机构信息

Department of Neurosurgery, Physiology and Neuroscience, New York, New York 10016, USA.

出版信息

Nat Commun. 2012;3:1172. doi: 10.1038/ncomms2144.

Abstract

Dopamine transmission is critical for exploratory motor behaviour. A key regulator is acetylcholine; forebrain acetylcholine regulates striatal dopamine release, whereas brainstem cholinergic inputs regulate the transition of dopamine neurons from tonic to burst firing modes. How these sources of cholinergic activity combine to control dopamine efflux and exploratory motor behaviour is unclear. Here we show that mice lacking total forebrain acetylcholine exhibit enhanced frequency-dependent striatal dopamine release and are hyperactive in a novel environment, whereas mice lacking rostral brainstem acetylcholine are hypoactive. Exploratory motor behaviour is normalized by the removal of both cholinergic sources. Involvement of dopamine in the exploratory motor phenotypes observed in these mutants is indicated by their altered sensitivity to the dopamine D2 receptor antagonist raclopride. These results support a model in which forebrain and brainstem cholinergic systems act in tandem to regulate striatal dopamine signalling for proper control of motor activity.

摘要

多巴胺传递对于探索性运动行为至关重要。乙酰胆碱是关键的调节因子;前脑乙酰胆碱调节纹状体多巴胺的释放,而脑干胆碱能输入调节多巴胺神经元从持续放电模式向爆发放电模式的转变。这些胆碱能活动源如何结合起来控制多巴胺外排和探索性运动行为尚不清楚。在这里,我们表明,缺乏总前脑乙酰胆碱的小鼠表现出增强的频率依赖性纹状体多巴胺释放,并在新环境中过度活跃,而缺乏脑干前部乙酰胆碱的小鼠则活动减少。通过去除两种胆碱能来源,探索性运动行为恢复正常。这些突变体中观察到的多巴胺在探索性运动表型中的作用表明,它们对多巴胺 D2 受体拮抗剂氯丙嗪的敏感性发生了改变。这些结果支持一个模型,即前脑和脑干胆碱能系统协同作用,调节纹状体多巴胺信号,以正确控制运动活动。

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