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Distinct extended amygdala circuits for divergent motivational states

The comorbidity of anxiety and dysfunctional reward processing in illnesses such as addiction(1) and depression(2) suggests that common neural circuitry contributes to these disparate neuropsychiatric symptoms. The extended amygdala, including the bed nucleus of the stria terminalis (BNST), modulate...

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Autores principales: Jennings, Joshua H., Sparta, Dennis R., Stamatakis, Alice M., Ung, Randall L., Pleil, Kristen E., Kash, Thomas L., Stuber, Garret D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778934/
https://www.ncbi.nlm.nih.gov/pubmed/23515155
http://dx.doi.org/10.1038/nature12041
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author Jennings, Joshua H.
Sparta, Dennis R.
Stamatakis, Alice M.
Ung, Randall L.
Pleil, Kristen E.
Kash, Thomas L.
Stuber, Garret D.
author_facet Jennings, Joshua H.
Sparta, Dennis R.
Stamatakis, Alice M.
Ung, Randall L.
Pleil, Kristen E.
Kash, Thomas L.
Stuber, Garret D.
author_sort Jennings, Joshua H.
collection PubMed
description The comorbidity of anxiety and dysfunctional reward processing in illnesses such as addiction(1) and depression(2) suggests that common neural circuitry contributes to these disparate neuropsychiatric symptoms. The extended amygdala, including the bed nucleus of the stria terminalis (BNST), modulates fear and anxiety(3,4), but also projects to the ventral tegmental area (VTA) (5,6), a region implicated in reward and aversion(7–13), thus providing a candidate neural substrate for integrating diverse emotional states. However, the precise functional connectivity between distinct BNST projection neurons and their postsynaptic targets in the VTA, as well as the role of this circuit in controlling motivational states have not been described. Here, we recorded and manipulated the activity of genetically and neurochemically identified VTA-projecting BNST neurons in freely behaving mice. Collectively, aversive stimuli exposure produced heterogeneous firing patterns in VTA-projecting BNST neurons. In contrast, in vivo optically-identified glutamatergic projection neurons displayed a net enhancement of activity to aversive stimuli, whereas the firing rate of identified GABAergic projection neurons was suppressed. Channelrhodopsin-2 (ChR2) assisted circuit mapping revealed that both BNST glutamatergic and GABAergic projections preferentially innervate postsynaptic non-dopaminergic VTA neurons, thus providing a mechanistic framework for in vivo circuit perturbations. In vivo photostimulation of BNST glutamatergic projections resulted in aversive and anxiogenic behavioral phenotypes. In contrast, activation of BNST GABAergic projections produced rewarding and anxiolytic phenotypes, which were also recapitulated by direct inhibition of VTA GABAergic neurons. These data demonstrate that functionally opposing BNST to VTA circuits regulate rewarding and aversive motivational states and may serve as a critical circuit node for bidirectionally normalizing maladaptive behaviors.
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spelling pubmed-37789342013-10-11 Distinct extended amygdala circuits for divergent motivational states Jennings, Joshua H. Sparta, Dennis R. Stamatakis, Alice M. Ung, Randall L. Pleil, Kristen E. Kash, Thomas L. Stuber, Garret D. Nature Article The comorbidity of anxiety and dysfunctional reward processing in illnesses such as addiction(1) and depression(2) suggests that common neural circuitry contributes to these disparate neuropsychiatric symptoms. The extended amygdala, including the bed nucleus of the stria terminalis (BNST), modulates fear and anxiety(3,4), but also projects to the ventral tegmental area (VTA) (5,6), a region implicated in reward and aversion(7–13), thus providing a candidate neural substrate for integrating diverse emotional states. However, the precise functional connectivity between distinct BNST projection neurons and their postsynaptic targets in the VTA, as well as the role of this circuit in controlling motivational states have not been described. Here, we recorded and manipulated the activity of genetically and neurochemically identified VTA-projecting BNST neurons in freely behaving mice. Collectively, aversive stimuli exposure produced heterogeneous firing patterns in VTA-projecting BNST neurons. In contrast, in vivo optically-identified glutamatergic projection neurons displayed a net enhancement of activity to aversive stimuli, whereas the firing rate of identified GABAergic projection neurons was suppressed. Channelrhodopsin-2 (ChR2) assisted circuit mapping revealed that both BNST glutamatergic and GABAergic projections preferentially innervate postsynaptic non-dopaminergic VTA neurons, thus providing a mechanistic framework for in vivo circuit perturbations. In vivo photostimulation of BNST glutamatergic projections resulted in aversive and anxiogenic behavioral phenotypes. In contrast, activation of BNST GABAergic projections produced rewarding and anxiolytic phenotypes, which were also recapitulated by direct inhibition of VTA GABAergic neurons. These data demonstrate that functionally opposing BNST to VTA circuits regulate rewarding and aversive motivational states and may serve as a critical circuit node for bidirectionally normalizing maladaptive behaviors. 2013-03-20 2013-04-11 /pmc/articles/PMC3778934/ /pubmed/23515155 http://dx.doi.org/10.1038/nature12041 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Jennings, Joshua H.
Sparta, Dennis R.
Stamatakis, Alice M.
Ung, Randall L.
Pleil, Kristen E.
Kash, Thomas L.
Stuber, Garret D.
Distinct extended amygdala circuits for divergent motivational states
title Distinct extended amygdala circuits for divergent motivational states
title_full Distinct extended amygdala circuits for divergent motivational states
title_fullStr Distinct extended amygdala circuits for divergent motivational states
title_full_unstemmed Distinct extended amygdala circuits for divergent motivational states
title_short Distinct extended amygdala circuits for divergent motivational states
title_sort distinct extended amygdala circuits for divergent motivational states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778934/
https://www.ncbi.nlm.nih.gov/pubmed/23515155
http://dx.doi.org/10.1038/nature12041
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