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Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety

The hippocampus (1–7), as well as dopamine circuits (8–11), coordinate decision-making in anxiety-eliciting situations. Yet, little is known about how dopamine modulates hippocampal representations of emotionally-salient stimuli to inform appropriate resolution of approach versus avoidance conflicts...

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Autores principales: Godino, Arthur, Salery, Marine, Minier-Toribio, Angelica M., Patel, Vishwendra, Fullard, John F., Parise, Eric M., Martinez-Rivera, Freddyson J., Morel, Carole, Roussos, Panos, Blitzer, Robert D., Nestler, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402022/
https://www.ncbi.nlm.nih.gov/pubmed/37546856
http://dx.doi.org/10.1101/2023.07.25.550554
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author Godino, Arthur
Salery, Marine
Minier-Toribio, Angelica M.
Patel, Vishwendra
Fullard, John F.
Parise, Eric M.
Martinez-Rivera, Freddyson J.
Morel, Carole
Roussos, Panos
Blitzer, Robert D.
Nestler, Eric J.
author_facet Godino, Arthur
Salery, Marine
Minier-Toribio, Angelica M.
Patel, Vishwendra
Fullard, John F.
Parise, Eric M.
Martinez-Rivera, Freddyson J.
Morel, Carole
Roussos, Panos
Blitzer, Robert D.
Nestler, Eric J.
author_sort Godino, Arthur
collection PubMed
description The hippocampus (1–7), as well as dopamine circuits (8–11), coordinate decision-making in anxiety-eliciting situations. Yet, little is known about how dopamine modulates hippocampal representations of emotionally-salient stimuli to inform appropriate resolution of approach versus avoidance conflicts. We here study dopaminoceptive neurons in mouse ventral hippocampus (vHipp), molecularly distinguished by their expression of dopamine D1 or D2 receptors. We show that these neurons are transcriptionally distinct and topographically organized across vHipp subfields and cell types. In the ventral subiculum where they are enriched, both D1 and D2 neurons are recruited during anxiogenic exploration, yet with distinct profiles related to investigation and behavioral selection. In turn, they mediate opposite approach/avoidance responses, and are differentially modulated by dopaminergic transmission in that region. Together, these results suggest that vHipp dopamine dynamics gate exploratory behaviors under contextual uncertainty, implicating dopaminoception in the complex computation engaged in vHipp to govern emotional states.
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spelling pubmed-104020222023-08-05 Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety Godino, Arthur Salery, Marine Minier-Toribio, Angelica M. Patel, Vishwendra Fullard, John F. Parise, Eric M. Martinez-Rivera, Freddyson J. Morel, Carole Roussos, Panos Blitzer, Robert D. Nestler, Eric J. bioRxiv Article The hippocampus (1–7), as well as dopamine circuits (8–11), coordinate decision-making in anxiety-eliciting situations. Yet, little is known about how dopamine modulates hippocampal representations of emotionally-salient stimuli to inform appropriate resolution of approach versus avoidance conflicts. We here study dopaminoceptive neurons in mouse ventral hippocampus (vHipp), molecularly distinguished by their expression of dopamine D1 or D2 receptors. We show that these neurons are transcriptionally distinct and topographically organized across vHipp subfields and cell types. In the ventral subiculum where they are enriched, both D1 and D2 neurons are recruited during anxiogenic exploration, yet with distinct profiles related to investigation and behavioral selection. In turn, they mediate opposite approach/avoidance responses, and are differentially modulated by dopaminergic transmission in that region. Together, these results suggest that vHipp dopamine dynamics gate exploratory behaviors under contextual uncertainty, implicating dopaminoception in the complex computation engaged in vHipp to govern emotional states. Cold Spring Harbor Laboratory 2023-07-28 /pmc/articles/PMC10402022/ /pubmed/37546856 http://dx.doi.org/10.1101/2023.07.25.550554 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Godino, Arthur
Salery, Marine
Minier-Toribio, Angelica M.
Patel, Vishwendra
Fullard, John F.
Parise, Eric M.
Martinez-Rivera, Freddyson J.
Morel, Carole
Roussos, Panos
Blitzer, Robert D.
Nestler, Eric J.
Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title_full Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title_fullStr Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title_full_unstemmed Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title_short Dopaminoceptive D1 and D2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
title_sort dopaminoceptive d1 and d2 neurons in ventral hippocampus arbitrate approach and avoidance in anxiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402022/
https://www.ncbi.nlm.nih.gov/pubmed/37546856
http://dx.doi.org/10.1101/2023.07.25.550554
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