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Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation

Across species, motivated states such as food-seeking and consumption are essential for survival. The lateral hypothalamus (LH) is known to play a fundamental role in regulating feeding and reward-related behaviors. However, the contributions of neuronal subpopulations in the LH have not been thorou...

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Autores principales: Schiffino, Felipe L., Siemian, Justin N., Petrella, Michele, Laing, Brenton T., Sarsfield, Sarah, Borja, Cara B., Gajendiran, Anjali, Zuccoli, Maria Laura, Aponte, Yeka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619795/
https://www.ncbi.nlm.nih.gov/pubmed/31291348
http://dx.doi.org/10.1371/journal.pone.0219522
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author Schiffino, Felipe L.
Siemian, Justin N.
Petrella, Michele
Laing, Brenton T.
Sarsfield, Sarah
Borja, Cara B.
Gajendiran, Anjali
Zuccoli, Maria Laura
Aponte, Yeka
author_facet Schiffino, Felipe L.
Siemian, Justin N.
Petrella, Michele
Laing, Brenton T.
Sarsfield, Sarah
Borja, Cara B.
Gajendiran, Anjali
Zuccoli, Maria Laura
Aponte, Yeka
author_sort Schiffino, Felipe L.
collection PubMed
description Across species, motivated states such as food-seeking and consumption are essential for survival. The lateral hypothalamus (LH) is known to play a fundamental role in regulating feeding and reward-related behaviors. However, the contributions of neuronal subpopulations in the LH have not been thoroughly identified. Here we examine how lateral hypothalamic leptin receptor-expressing (LH(LEPR)) neurons, a subset of GABAergic cells, regulate motivation in mice. We find that LH(LEPR) neuronal activation significantly increases progressive ratio (PR) performance, while inhibition decreases responding. Moreover, we mapped LH(LEPR) axonal projections and demonstrated that they target the ventral tegmental area (VTA), form functional inhibitory synapses with non-dopaminergic VTA neurons, and their activation promotes motivation for food. Finally, we find that LH(LEPR) neurons also regulate motivation to obtain water, suggesting that they may play a generalized role in motivation. Together, these results identify LH(LEPR) neurons as modulators within a hypothalamic-ventral tegmental circuit that gates motivation.
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spelling pubmed-66197952019-07-25 Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation Schiffino, Felipe L. Siemian, Justin N. Petrella, Michele Laing, Brenton T. Sarsfield, Sarah Borja, Cara B. Gajendiran, Anjali Zuccoli, Maria Laura Aponte, Yeka PLoS One Research Article Across species, motivated states such as food-seeking and consumption are essential for survival. The lateral hypothalamus (LH) is known to play a fundamental role in regulating feeding and reward-related behaviors. However, the contributions of neuronal subpopulations in the LH have not been thoroughly identified. Here we examine how lateral hypothalamic leptin receptor-expressing (LH(LEPR)) neurons, a subset of GABAergic cells, regulate motivation in mice. We find that LH(LEPR) neuronal activation significantly increases progressive ratio (PR) performance, while inhibition decreases responding. Moreover, we mapped LH(LEPR) axonal projections and demonstrated that they target the ventral tegmental area (VTA), form functional inhibitory synapses with non-dopaminergic VTA neurons, and their activation promotes motivation for food. Finally, we find that LH(LEPR) neurons also regulate motivation to obtain water, suggesting that they may play a generalized role in motivation. Together, these results identify LH(LEPR) neurons as modulators within a hypothalamic-ventral tegmental circuit that gates motivation. Public Library of Science 2019-07-10 /pmc/articles/PMC6619795/ /pubmed/31291348 http://dx.doi.org/10.1371/journal.pone.0219522 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Schiffino, Felipe L.
Siemian, Justin N.
Petrella, Michele
Laing, Brenton T.
Sarsfield, Sarah
Borja, Cara B.
Gajendiran, Anjali
Zuccoli, Maria Laura
Aponte, Yeka
Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title_full Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title_fullStr Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title_full_unstemmed Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title_short Activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
title_sort activation of a lateral hypothalamic-ventral tegmental circuit gates motivation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619795/
https://www.ncbi.nlm.nih.gov/pubmed/31291348
http://dx.doi.org/10.1371/journal.pone.0219522
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