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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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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. |
format | Online Article Text |
id | pubmed-6619795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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