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dc.contributor.author Lee, Joo Han -
dc.contributor.author Ribeiro, Efrain A. -
dc.contributor.author Kim, Jeong Seop -
dc.contributor.author Ko, Bumjin -
dc.contributor.author Kronman, Hope -
dc.contributor.author Ha Jeong, Yun -
dc.contributor.author Kim, Jong Kyoung -
dc.contributor.author Janak, Patricia H. -
dc.contributor.author Nestler, Eric J. -
dc.contributor.author Koo, Ja Wook -
dc.contributor.author Kim, Joung-Hun -
dc.date.accessioned 2021-01-22T07:10:27Z -
dc.date.available 2021-01-22T07:10:27Z -
dc.date.created 2020-07-30 -
dc.date.issued 2020-11 -
dc.identifier.citation Biological Psychiatry, v.88, no.10, pp.746 - 757 -
dc.identifier.issn 0006-3223 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/12688 -
dc.description.abstract Background: Cholinergic interneurons (ChINs) in the nucleus accumbens (NAc) play critical roles in processing information related to reward. However, the contribution of ChINs to the emergence of addiction-like behaviors and its underlying molecular mechanisms remain elusive. Methods: We employed cocaine self-administration to identify two mouse subpopulations: susceptible and resilient to cocaine seeking. We compared the subpopulations for physiological responses with single-unit recording of NAc ChINs, and for gene expression levels with RNA sequencing of ChINs sorted using fluorescence-activated cell sorting. To provide evidence for a causal relationship, we manipulated the expression level of dopamine D2 receptor (DRD2) in ChINs in a cell type–specific manner. Using optogenetic activation combined with a double whole-cell recording, the effect of ChIN-specific DRD2 manipulation on each synaptic input was assessed in NAc medium spiny neurons in a pathway-specific manner. Results: Susceptible mice showed higher levels of nosepoke responses under a progressive ratio schedule, and impairment in extinction and punishment procedures. DRD2 was highly abundant in the NAc ChINs of susceptible mice. Elevated abundance of DRD2 in NAc ChINs was sufficient and necessary to express high cocaine motivation, putatively through reduction of ChIN activity during cocaine exposure. DRD2 overexpression in ChINs mimicked cocaine-induced effects on the dendritic spine density and the ratios of excitatory inputs between two distinct medium spiny neuron cell types, while DRD2 depletion precluded cocaine-induced synaptic plasticity. Conclusions: These findings provide a molecular mechanism for dopaminergic control of NAc ChINs that can control the susceptibility to cocaine-seeking behavior. © 2020 Society of Biological Psychiatry -
dc.language English -
dc.publisher Elsevier BV -
dc.title Dopaminergic Regulation of Nucleus Accumbens Cholinergic Interneurons Demarcates Susceptibility to Cocaine Addiction -
dc.type Article -
dc.identifier.doi 10.1016/j.biopsych.2020.05.003 -
dc.identifier.wosid 000579903000006 -
dc.identifier.scopusid 2-s2.0-85087211065 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.citation.publicationname Biological Psychiatry -
dc.contributor.nonIdAuthor Lee, Joo Han -
dc.contributor.nonIdAuthor Ribeiro, Efrain A. -
dc.contributor.nonIdAuthor Kim, Jeong Seop -
dc.contributor.nonIdAuthor Ko, Bumjin -
dc.contributor.nonIdAuthor Kronman, Hope -
dc.contributor.nonIdAuthor Ha Jeong, Yun -
dc.contributor.nonIdAuthor Janak, Patricia H. -
dc.contributor.nonIdAuthor Nestler, Eric J. -
dc.contributor.nonIdAuthor Koo, Ja Wook -
dc.contributor.nonIdAuthor Kim, Joung-Hun -
dc.identifier.citationVolume 88 -
dc.identifier.citationNumber 10 -
dc.identifier.citationStartPage 746 -
dc.identifier.citationEndPage 757 -
dc.identifier.citationTitle Biological Psychiatry -
dc.type.journalArticle Article -
dc.description.isOpenAccess N -
dc.subject.keywordAuthor Cholinergic interneurons -
dc.subject.keywordAuthor Cocaine addiction -
dc.subject.keywordAuthor Dopamine D2 receptor -
dc.subject.keywordAuthor Medium spiny neurons -
dc.subject.keywordAuthor Nucleus accumbens -
dc.subject.keywordAuthor Synaptic plasticity -
dc.subject.keywordPlus RECEPTOR -
dc.subject.keywordPlus NEURONS -
dc.subject.keywordPlus MODULATION -
dc.subject.keywordPlus PLASTICITY -
dc.subject.keywordPlus STRIATUM -
dc.subject.keywordPlus D2 -
dc.subject.keywordPlus ACTIVATION -
dc.subject.keywordPlus MECHANISMS -
dc.subject.keywordPlus DORSAL -
dc.contributor.affiliatedAuthor Lee, Joo Han -
dc.contributor.affiliatedAuthor Ribeiro, Efrain A. -
dc.contributor.affiliatedAuthor Kim, Jeong Seop -
dc.contributor.affiliatedAuthor Ko, Bumjin -
dc.contributor.affiliatedAuthor Kronman, Hope -
dc.contributor.affiliatedAuthor Ha Jeong, Yun -
dc.contributor.affiliatedAuthor Kim, Jong Kyoung -
dc.contributor.affiliatedAuthor Janak, Patricia H. -
dc.contributor.affiliatedAuthor Nestler, Eric J. -
dc.contributor.affiliatedAuthor Koo, Ja Wook -
dc.contributor.affiliatedAuthor Kim, Joung-Hun -
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Department of New Biology Laboratory of Single-Cell Genomics 1. Journal Articles

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