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The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens
We examine synaptic connectivity and cocaine-evoked plasticity at specific networks within the nucleus accumbens (NAc). We identify distinct subpopulations of D1+ medium spiny neurons (MSNs) that project to either the ventral pallidum (D1+(VP)) or the ventral tegmental area (D1+(VTA)). We show that...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733522/ https://www.ncbi.nlm.nih.gov/pubmed/31461643 http://dx.doi.org/10.1016/j.celrep.2019.07.074 |
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author | Baimel, Corey McGarry, Laura M. Carter, Adam G. |
author_facet | Baimel, Corey McGarry, Laura M. Carter, Adam G. |
author_sort | Baimel, Corey |
collection | PubMed |
description | We examine synaptic connectivity and cocaine-evoked plasticity at specific networks within the nucleus accumbens (NAc). We identify distinct subpopulations of D1+ medium spiny neurons (MSNs) that project to either the ventral pallidum (D1+(VP)) or the ventral tegmental area (D1+(VTA)). We show that inputs from the ventral hippocampus (vHPC), but not the basolateral amygdala (BLA), are initially biased onto D1+(VTA) MSNs. However, repeated cocaine exposure eliminates the bias of vHPC inputs onto D1+(VTA) MSNs, while strengthening BLA inputs onto D1+(VP) MSNs. Our results reveal that connectivity and plasticity depend on the specific inputs and outputs of D1+ MSNs and highlight the complexity of cocaine-evoked circuit level adaptations in the NAc. |
format | Online Article Text |
id | pubmed-6733522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-67335222019-09-09 The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens Baimel, Corey McGarry, Laura M. Carter, Adam G. Cell Rep Article We examine synaptic connectivity and cocaine-evoked plasticity at specific networks within the nucleus accumbens (NAc). We identify distinct subpopulations of D1+ medium spiny neurons (MSNs) that project to either the ventral pallidum (D1+(VP)) or the ventral tegmental area (D1+(VTA)). We show that inputs from the ventral hippocampus (vHPC), but not the basolateral amygdala (BLA), are initially biased onto D1+(VTA) MSNs. However, repeated cocaine exposure eliminates the bias of vHPC inputs onto D1+(VTA) MSNs, while strengthening BLA inputs onto D1+(VP) MSNs. Our results reveal that connectivity and plasticity depend on the specific inputs and outputs of D1+ MSNs and highlight the complexity of cocaine-evoked circuit level adaptations in the NAc. 2019-08-27 /pmc/articles/PMC6733522/ /pubmed/31461643 http://dx.doi.org/10.1016/j.celrep.2019.07.074 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Baimel, Corey McGarry, Laura M. Carter, Adam G. The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title | The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title_full | The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title_fullStr | The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title_full_unstemmed | The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title_short | The Projection Targets of Medium Spiny Neurons Govern Cocaine-Evoked Synaptic Plasticity in the Nucleus Accumbens |
title_sort | projection targets of medium spiny neurons govern cocaine-evoked synaptic plasticity in the nucleus accumbens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733522/ https://www.ncbi.nlm.nih.gov/pubmed/31461643 http://dx.doi.org/10.1016/j.celrep.2019.07.074 |
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