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Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice

Food consumption is necessary for organisms to maintain metabolic homeostasis. Both extrinsic and intrinsic processes, relayed via intricate neural circuitry, orchestrate the initiation and termination of food intake. More specifically, there are functionally distinct neural circuits that mediate ei...

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Autores principales: Rodriguez, Erica, Ryu, David, Zhao, Shengli, Han, Bao-Xia, Wang, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868176/
https://www.ncbi.nlm.nih.gov/pubmed/31662323
http://dx.doi.org/10.1523/ENEURO.0252-19.2019
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author Rodriguez, Erica
Ryu, David
Zhao, Shengli
Han, Bao-Xia
Wang, Fan
author_facet Rodriguez, Erica
Ryu, David
Zhao, Shengli
Han, Bao-Xia
Wang, Fan
author_sort Rodriguez, Erica
collection PubMed
description Food consumption is necessary for organisms to maintain metabolic homeostasis. Both extrinsic and intrinsic processes, relayed via intricate neural circuitry, orchestrate the initiation and termination of food intake. More specifically, there are functionally distinct neural circuits that mediate either homeostatic or hedonic suppression of feeding. Notably, being satiated is a positive feeling whereas food aversion is a negative feeling. While significant progress has been made toward elucidating neural circuitry underlying aversive appetite suppression in mice, the circuitry underlying homeostatic satiety is not fully understood. The lateral parabrachial nucleus (PB(L)) is known as a node that regulates various sensory and visceral processes. Here, we identified and selectively labeled neurons in the caudal lateral region of PB(L) (PB(cl)) that are activated by consumption of condensed milk, chocolate Ensure, or peanut butter, which we refer to as PB(cl)-palatable-food activated neurons (PANs). Specific optogenetic activation of PANs induced positive place preference but decreased the consumption of high-caloric foods such as condensed milk, whereas silencing these cells significantly increased condensed milk consumption in feeding assays. Thus, the PB(cl) PANs revealed here represent a novel neural substrate regulating caloric-sufficiency mediated satiation.
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spelling pubmed-68681762019-11-21 Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice Rodriguez, Erica Ryu, David Zhao, Shengli Han, Bao-Xia Wang, Fan eNeuro New Research Food consumption is necessary for organisms to maintain metabolic homeostasis. Both extrinsic and intrinsic processes, relayed via intricate neural circuitry, orchestrate the initiation and termination of food intake. More specifically, there are functionally distinct neural circuits that mediate either homeostatic or hedonic suppression of feeding. Notably, being satiated is a positive feeling whereas food aversion is a negative feeling. While significant progress has been made toward elucidating neural circuitry underlying aversive appetite suppression in mice, the circuitry underlying homeostatic satiety is not fully understood. The lateral parabrachial nucleus (PB(L)) is known as a node that regulates various sensory and visceral processes. Here, we identified and selectively labeled neurons in the caudal lateral region of PB(L) (PB(cl)) that are activated by consumption of condensed milk, chocolate Ensure, or peanut butter, which we refer to as PB(cl)-palatable-food activated neurons (PANs). Specific optogenetic activation of PANs induced positive place preference but decreased the consumption of high-caloric foods such as condensed milk, whereas silencing these cells significantly increased condensed milk consumption in feeding assays. Thus, the PB(cl) PANs revealed here represent a novel neural substrate regulating caloric-sufficiency mediated satiation. Society for Neuroscience 2019-11-19 /pmc/articles/PMC6868176/ /pubmed/31662323 http://dx.doi.org/10.1523/ENEURO.0252-19.2019 Text en Copyright © 2019 Rodriguez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle New Research
Rodriguez, Erica
Ryu, David
Zhao, Shengli
Han, Bao-Xia
Wang, Fan
Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title_full Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title_fullStr Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title_full_unstemmed Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title_short Identifying Parabrachial Neurons Selectively Regulating Satiety for Highly Palatable Food in Mice
title_sort identifying parabrachial neurons selectively regulating satiety for highly palatable food in mice
topic New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868176/
https://www.ncbi.nlm.nih.gov/pubmed/31662323
http://dx.doi.org/10.1523/ENEURO.0252-19.2019
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