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Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens
The ventral tegmental area (VTA) projection to the nucleus accumbens shell (NAcSh) regulates NAcSh-mediated motivated behaviors in part by modulating the glutamatergic inputs. This modulation is likely to be mediated by multiple substances released from VTA axons, whose phenotypic diversity is illus...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895172/ https://www.ncbi.nlm.nih.gov/pubmed/31804595 http://dx.doi.org/10.1038/s41598-019-55007-y |
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author | Yu, Jun Ishikawa, Masago Wang, Junshi Schlüter, Oliver M. Sesack, Susan R. Dong, Yan |
author_facet | Yu, Jun Ishikawa, Masago Wang, Junshi Schlüter, Oliver M. Sesack, Susan R. Dong, Yan |
author_sort | Yu, Jun |
collection | PubMed |
description | The ventral tegmental area (VTA) projection to the nucleus accumbens shell (NAcSh) regulates NAcSh-mediated motivated behaviors in part by modulating the glutamatergic inputs. This modulation is likely to be mediated by multiple substances released from VTA axons, whose phenotypic diversity is illustrated here by ultrastructural examination. Furthermore, we show in mouse brain slices that a brief optogenetic stimulation of VTA-to-NAc projection induced a transient inhibition of excitatory postsynaptic currents (EPSCs) in NAcSh principal medium spiny neurons (MSNs). This inhibition was not accompanied by detectable alterations in presynaptic release properties of electrically-evoked EPSCs, suggesting a postsynaptic mechanism. The VTA projection to the NAcSh releases dopamine, GABA and glutamate, and induces the release of other neuronal substrates that are capable of regulating synaptic transmission. However, pharmacological inhibition of dopamine D1 or D2 receptors, GABAA or GABAB receptors, NMDA receptors, P2Y1 ATP receptors, metabotropic glutamate receptor 5, and TRP channels did not prevent this short-term inhibition. These results suggest that an unknown mechanism mediates this form of short-term plasticity induced by the VTA-to-NAc projection. |
format | Online Article Text |
id | pubmed-6895172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68951722019-12-12 Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens Yu, Jun Ishikawa, Masago Wang, Junshi Schlüter, Oliver M. Sesack, Susan R. Dong, Yan Sci Rep Article The ventral tegmental area (VTA) projection to the nucleus accumbens shell (NAcSh) regulates NAcSh-mediated motivated behaviors in part by modulating the glutamatergic inputs. This modulation is likely to be mediated by multiple substances released from VTA axons, whose phenotypic diversity is illustrated here by ultrastructural examination. Furthermore, we show in mouse brain slices that a brief optogenetic stimulation of VTA-to-NAc projection induced a transient inhibition of excitatory postsynaptic currents (EPSCs) in NAcSh principal medium spiny neurons (MSNs). This inhibition was not accompanied by detectable alterations in presynaptic release properties of electrically-evoked EPSCs, suggesting a postsynaptic mechanism. The VTA projection to the NAcSh releases dopamine, GABA and glutamate, and induces the release of other neuronal substrates that are capable of regulating synaptic transmission. However, pharmacological inhibition of dopamine D1 or D2 receptors, GABAA or GABAB receptors, NMDA receptors, P2Y1 ATP receptors, metabotropic glutamate receptor 5, and TRP channels did not prevent this short-term inhibition. These results suggest that an unknown mechanism mediates this form of short-term plasticity induced by the VTA-to-NAc projection. Nature Publishing Group UK 2019-12-05 /pmc/articles/PMC6895172/ /pubmed/31804595 http://dx.doi.org/10.1038/s41598-019-55007-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Jun Ishikawa, Masago Wang, Junshi Schlüter, Oliver M. Sesack, Susan R. Dong, Yan Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title | Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title_full | Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title_fullStr | Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title_full_unstemmed | Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title_short | Ventral Tegmental Area Projection Regulates Glutamatergic Transmission in Nucleus Accumbens |
title_sort | ventral tegmental area projection regulates glutamatergic transmission in nucleus accumbens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895172/ https://www.ncbi.nlm.nih.gov/pubmed/31804595 http://dx.doi.org/10.1038/s41598-019-55007-y |
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