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A limbic circuit selectively links active escape to food suppression
Stress has pleiotropic physiologic effects, but the neural circuits linking stress to these responses are not well understood. Here, we describe a novel population of lateral septum neurons expressing neurotensin (LS(Nts)) in mice that are selectively tuned to specific types of stress. LS(Nts) neuro...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476759/ https://www.ncbi.nlm.nih.gov/pubmed/32894221 http://dx.doi.org/10.7554/eLife.58894 |
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author | Azevedo, Estefania P Tan, Bowen Pomeranz, Lisa E Ivan, Violet Fetcho, Robert Schneeberger, Marc Doerig, Katherine R Liston, Conor Friedman, Jeffrey M Stern, Sarah A |
author_facet | Azevedo, Estefania P Tan, Bowen Pomeranz, Lisa E Ivan, Violet Fetcho, Robert Schneeberger, Marc Doerig, Katherine R Liston, Conor Friedman, Jeffrey M Stern, Sarah A |
author_sort | Azevedo, Estefania P |
collection | PubMed |
description | Stress has pleiotropic physiologic effects, but the neural circuits linking stress to these responses are not well understood. Here, we describe a novel population of lateral septum neurons expressing neurotensin (LS(Nts)) in mice that are selectively tuned to specific types of stress. LS(Nts) neurons increase their activity during active escape, responding to stress when flight is a viable option, but not when associated with freezing or immobility. Chemogenetic activation of LS(Nts) neurons decreases food intake and body weight, without altering locomotion and anxiety. LS(Nts) neurons co-express several molecules including Glp1r (glucagon-like peptide one receptor) and manipulations of Glp1r signaling in the LS recapitulates the behavioral effects of LS(Nts) activation. Activation of LS(Nts) terminals in the lateral hypothalamus (LH) also decreases food intake. These results show that LS(Nts) neurons are selectively tuned to active escape stress and can reduce food consumption via effects on hypothalamic pathways. |
format | Online Article Text |
id | pubmed-7476759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-74767592020-09-09 A limbic circuit selectively links active escape to food suppression Azevedo, Estefania P Tan, Bowen Pomeranz, Lisa E Ivan, Violet Fetcho, Robert Schneeberger, Marc Doerig, Katherine R Liston, Conor Friedman, Jeffrey M Stern, Sarah A eLife Neuroscience Stress has pleiotropic physiologic effects, but the neural circuits linking stress to these responses are not well understood. Here, we describe a novel population of lateral septum neurons expressing neurotensin (LS(Nts)) in mice that are selectively tuned to specific types of stress. LS(Nts) neurons increase their activity during active escape, responding to stress when flight is a viable option, but not when associated with freezing or immobility. Chemogenetic activation of LS(Nts) neurons decreases food intake and body weight, without altering locomotion and anxiety. LS(Nts) neurons co-express several molecules including Glp1r (glucagon-like peptide one receptor) and manipulations of Glp1r signaling in the LS recapitulates the behavioral effects of LS(Nts) activation. Activation of LS(Nts) terminals in the lateral hypothalamus (LH) also decreases food intake. These results show that LS(Nts) neurons are selectively tuned to active escape stress and can reduce food consumption via effects on hypothalamic pathways. eLife Sciences Publications, Ltd 2020-09-07 /pmc/articles/PMC7476759/ /pubmed/32894221 http://dx.doi.org/10.7554/eLife.58894 Text en © 2020, Azevedo et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Azevedo, Estefania P Tan, Bowen Pomeranz, Lisa E Ivan, Violet Fetcho, Robert Schneeberger, Marc Doerig, Katherine R Liston, Conor Friedman, Jeffrey M Stern, Sarah A A limbic circuit selectively links active escape to food suppression |
title | A limbic circuit selectively links active escape to food suppression |
title_full | A limbic circuit selectively links active escape to food suppression |
title_fullStr | A limbic circuit selectively links active escape to food suppression |
title_full_unstemmed | A limbic circuit selectively links active escape to food suppression |
title_short | A limbic circuit selectively links active escape to food suppression |
title_sort | limbic circuit selectively links active escape to food suppression |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476759/ https://www.ncbi.nlm.nih.gov/pubmed/32894221 http://dx.doi.org/10.7554/eLife.58894 |
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