多巴胺
被盖腹侧区
神经科学
长时程增强
神经传递
生物
化学
多巴胺能
生物化学
受体
作者
Christina Bocklisch,Vincent Pascoli,Jovi C. Y. Wong,David Richard Clermont House,Cédric Yvon,Mathias De Roo,Kelly R. Tan,Christian Lüscher
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-09-26
卷期号:341 (6153): 1521-1525
被引量:310
标识
DOI:10.1126/science.1237059
摘要
Drug-evoked synaptic plasticity in the mesolimbic system reshapes circuit function and drives drug-adaptive behavior. Much research has focused on excitatory transmission in the ventral tegmental area (VTA) and the nucleus accumbens (NAc). How drug-evoked synaptic plasticity of inhibitory transmission affects circuit adaptations remains unknown. We found that medium spiny neurons expressing dopamine (DA) receptor type 1 (D1R-MSNs) of the NAc project to the VTA, strongly preferring the GABA neurons of the VTA. Repeated in vivo exposure to cocaine evoked synaptic potentiation at this synapse, occluding homosynaptic inhibitory long-term potentiation. The activity of the VTA GABA neurons was thus reduced and DA neurons were disinhibited. Cocaine-evoked potentiation of GABA release from D1R-MSNs affected drug-adaptive behavior, which identifies these neurons as a promising target for novel addiction treatments.
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