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An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake

It is well recognized that ventromedial hypothalamus (VMH) serves as a satiety center in the brain. However, the feeding circuit for the VMH regulation of food intake remains to be defined. Here, we combine fiber photometry, chemo/optogenetics, virus-assisted retrograde tracing, ChR2-assisted circui...

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Autores principales: Zhang, Jia, Chen, Dan, Sweeney, Patrick, Yang, Yunlei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728757/
https://www.ncbi.nlm.nih.gov/pubmed/33303759
http://dx.doi.org/10.1038/s41467-020-20093-4
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author Zhang, Jia
Chen, Dan
Sweeney, Patrick
Yang, Yunlei
author_facet Zhang, Jia
Chen, Dan
Sweeney, Patrick
Yang, Yunlei
author_sort Zhang, Jia
collection PubMed
description It is well recognized that ventromedial hypothalamus (VMH) serves as a satiety center in the brain. However, the feeding circuit for the VMH regulation of food intake remains to be defined. Here, we combine fiber photometry, chemo/optogenetics, virus-assisted retrograde tracing, ChR2-assisted circuit mapping and behavioral assays to show that selective activation of VMH neurons expressing steroidogenic factor 1 (SF1) rapidly inhibits food intake, VMH SF1 neurons project dense fibers to the paraventricular thalamus (PVT), selective chemo/optogenetic stimulation of the PVT-projecting SF1 neurons or their projections to the PVT inhibits food intake, and chemical genetic inactivation of PVT neurons diminishes SF1 neural inhibition of feeding. We also find that activation of SF1 neurons or their projections to the PVT elicits a flavor aversive effect, and selective optogenetic stimulation of ChR2-expressing SF1 projections to the PVT elicits direct excitatory postsynaptic currents. Together, our data reveal a neural circuit from VMH to PVT that inhibits food intake.
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spelling pubmed-77287572020-12-17 An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake Zhang, Jia Chen, Dan Sweeney, Patrick Yang, Yunlei Nat Commun Article It is well recognized that ventromedial hypothalamus (VMH) serves as a satiety center in the brain. However, the feeding circuit for the VMH regulation of food intake remains to be defined. Here, we combine fiber photometry, chemo/optogenetics, virus-assisted retrograde tracing, ChR2-assisted circuit mapping and behavioral assays to show that selective activation of VMH neurons expressing steroidogenic factor 1 (SF1) rapidly inhibits food intake, VMH SF1 neurons project dense fibers to the paraventricular thalamus (PVT), selective chemo/optogenetic stimulation of the PVT-projecting SF1 neurons or their projections to the PVT inhibits food intake, and chemical genetic inactivation of PVT neurons diminishes SF1 neural inhibition of feeding. We also find that activation of SF1 neurons or their projections to the PVT elicits a flavor aversive effect, and selective optogenetic stimulation of ChR2-expressing SF1 projections to the PVT elicits direct excitatory postsynaptic currents. Together, our data reveal a neural circuit from VMH to PVT that inhibits food intake. Nature Publishing Group UK 2020-12-10 /pmc/articles/PMC7728757/ /pubmed/33303759 http://dx.doi.org/10.1038/s41467-020-20093-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhang, Jia
Chen, Dan
Sweeney, Patrick
Yang, Yunlei
An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title_full An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title_fullStr An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title_full_unstemmed An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title_short An excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
title_sort excitatory ventromedial hypothalamus to paraventricular thalamus circuit that suppresses food intake
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728757/
https://www.ncbi.nlm.nih.gov/pubmed/33303759
http://dx.doi.org/10.1038/s41467-020-20093-4
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