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Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression

Enhanced glutamatergic transmission in the nucleus accumbens (NAc), a region critical for reward and motivation, has been implicated in the pathophysiology of depression; however, the afferent source of this increased glutamate tone is not known. The NAc receives glutamatergic inputs from the medial...

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Autores principales: Bagot, Rosemary C., Parise, Eric M., Peña, Catherine J., Zhang, Hong-Xing, Maze, Ian, Chaudhury, Dipesh, Persaud, Brianna, Cachope, Roger, Bolaños-Guzmán, Carlos A., Cheer, Joseph, Deisseroth, Karl, Han, Ming-Hu, Nestler, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430111/
https://www.ncbi.nlm.nih.gov/pubmed/25952660
http://dx.doi.org/10.1038/ncomms8062
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author Bagot, Rosemary C.
Parise, Eric M.
Peña, Catherine J.
Zhang, Hong-Xing
Maze, Ian
Chaudhury, Dipesh
Persaud, Brianna
Cachope, Roger
Bolaños-Guzmán, Carlos A.
Cheer, Joseph
Deisseroth, Karl
Han, Ming-Hu
Nestler, Eric J.
author_facet Bagot, Rosemary C.
Parise, Eric M.
Peña, Catherine J.
Zhang, Hong-Xing
Maze, Ian
Chaudhury, Dipesh
Persaud, Brianna
Cachope, Roger
Bolaños-Guzmán, Carlos A.
Cheer, Joseph
Deisseroth, Karl
Han, Ming-Hu
Nestler, Eric J.
author_sort Bagot, Rosemary C.
collection PubMed
description Enhanced glutamatergic transmission in the nucleus accumbens (NAc), a region critical for reward and motivation, has been implicated in the pathophysiology of depression; however, the afferent source of this increased glutamate tone is not known. The NAc receives glutamatergic inputs from the medial prefrontal cortex (mPFC), ventral hippocampus (vHIP) and basolateral amygdala (AMY). Here, we demonstrate that glutamatergic vHIP afferents to NAc regulate susceptibility to chronic social defeat stress (CSDS). We observe reduced activity in vHIP in mice resilient to CSDS. Furthermore, attenuation of vHIP-NAc transmission by optogenetic induction of long-term depression is pro-resilient, whereas acute enhancement of this input is pro-susceptible. This effect is specific to vHIP afferents to the NAc, as optogenetic stimulation of either mPFC or AMY afferents to the NAc is pro-resilient. These data indicate that vHIP afferents to NAc uniquely regulate susceptibility to CSDS, highlighting an important, novel circuit-specific mechanism in depression.
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spelling pubmed-44301112015-05-23 Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression Bagot, Rosemary C. Parise, Eric M. Peña, Catherine J. Zhang, Hong-Xing Maze, Ian Chaudhury, Dipesh Persaud, Brianna Cachope, Roger Bolaños-Guzmán, Carlos A. Cheer, Joseph Deisseroth, Karl Han, Ming-Hu Nestler, Eric J. Nat Commun Article Enhanced glutamatergic transmission in the nucleus accumbens (NAc), a region critical for reward and motivation, has been implicated in the pathophysiology of depression; however, the afferent source of this increased glutamate tone is not known. The NAc receives glutamatergic inputs from the medial prefrontal cortex (mPFC), ventral hippocampus (vHIP) and basolateral amygdala (AMY). Here, we demonstrate that glutamatergic vHIP afferents to NAc regulate susceptibility to chronic social defeat stress (CSDS). We observe reduced activity in vHIP in mice resilient to CSDS. Furthermore, attenuation of vHIP-NAc transmission by optogenetic induction of long-term depression is pro-resilient, whereas acute enhancement of this input is pro-susceptible. This effect is specific to vHIP afferents to the NAc, as optogenetic stimulation of either mPFC or AMY afferents to the NAc is pro-resilient. These data indicate that vHIP afferents to NAc uniquely regulate susceptibility to CSDS, highlighting an important, novel circuit-specific mechanism in depression. Nature Pub. Group 2015-05-08 /pmc/articles/PMC4430111/ /pubmed/25952660 http://dx.doi.org/10.1038/ncomms8062 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bagot, Rosemary C.
Parise, Eric M.
Peña, Catherine J.
Zhang, Hong-Xing
Maze, Ian
Chaudhury, Dipesh
Persaud, Brianna
Cachope, Roger
Bolaños-Guzmán, Carlos A.
Cheer, Joseph
Deisseroth, Karl
Han, Ming-Hu
Nestler, Eric J.
Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title_full Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title_fullStr Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title_full_unstemmed Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title_short Ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
title_sort ventral hippocampal afferents to the nucleus accumbens regulate susceptibility to depression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430111/
https://www.ncbi.nlm.nih.gov/pubmed/25952660
http://dx.doi.org/10.1038/ncomms8062
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