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Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales

Agouti-related-peptide (AgRP) neurons—interoceptive neurons in the arcuate nucleus of the hypothalamus (ARC)—are both necessary and sufficient for driving feeding behavior. To better understand the functional roles of AgRP neurons, we performed optetrode electrophysiological recordings from AgRP neu...

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Autores principales: Mandelblat-Cerf, Yael, Ramesh, Rohan N, Burgess, Christian R, Patella, Paola, Yang, Zongfang, Lowell, Bradford B, Andermann, Mark L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498165/
https://www.ncbi.nlm.nih.gov/pubmed/26159614
http://dx.doi.org/10.7554/eLife.07122
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author Mandelblat-Cerf, Yael
Ramesh, Rohan N
Burgess, Christian R
Patella, Paola
Yang, Zongfang
Lowell, Bradford B
Andermann, Mark L
author_facet Mandelblat-Cerf, Yael
Ramesh, Rohan N
Burgess, Christian R
Patella, Paola
Yang, Zongfang
Lowell, Bradford B
Andermann, Mark L
author_sort Mandelblat-Cerf, Yael
collection PubMed
description Agouti-related-peptide (AgRP) neurons—interoceptive neurons in the arcuate nucleus of the hypothalamus (ARC)—are both necessary and sufficient for driving feeding behavior. To better understand the functional roles of AgRP neurons, we performed optetrode electrophysiological recordings from AgRP neurons in awake, behaving AgRP-IRES-Cre mice. In free-feeding mice, we observed a fivefold increase in AgRP neuron firing with mounting caloric deficit in afternoon vs morning recordings. In food-restricted mice, as food became available, AgRP neuron firing dropped, yet remained elevated as compared to firing in sated mice. The rapid drop in spiking activity of AgRP neurons at meal onset may reflect a termination of the drive to find food, while residual, persistent spiking may reflect a sustained drive to consume food. Moreover, nearby neurons inhibited by AgRP neuron photostimulation, likely including satiety-promoting pro-opiomelanocortin (POMC) neurons, demonstrated opposite changes in spiking. Finally, firing of ARC neurons was also rapidly modulated within seconds of individual licks for liquid food. These findings suggest novel roles for antagonistic AgRP and POMC neurons in the regulation of feeding behaviors across multiple timescales. DOI: http://dx.doi.org/10.7554/eLife.07122.001
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spelling pubmed-44981652015-07-11 Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales Mandelblat-Cerf, Yael Ramesh, Rohan N Burgess, Christian R Patella, Paola Yang, Zongfang Lowell, Bradford B Andermann, Mark L eLife Neuroscience Agouti-related-peptide (AgRP) neurons—interoceptive neurons in the arcuate nucleus of the hypothalamus (ARC)—are both necessary and sufficient for driving feeding behavior. To better understand the functional roles of AgRP neurons, we performed optetrode electrophysiological recordings from AgRP neurons in awake, behaving AgRP-IRES-Cre mice. In free-feeding mice, we observed a fivefold increase in AgRP neuron firing with mounting caloric deficit in afternoon vs morning recordings. In food-restricted mice, as food became available, AgRP neuron firing dropped, yet remained elevated as compared to firing in sated mice. The rapid drop in spiking activity of AgRP neurons at meal onset may reflect a termination of the drive to find food, while residual, persistent spiking may reflect a sustained drive to consume food. Moreover, nearby neurons inhibited by AgRP neuron photostimulation, likely including satiety-promoting pro-opiomelanocortin (POMC) neurons, demonstrated opposite changes in spiking. Finally, firing of ARC neurons was also rapidly modulated within seconds of individual licks for liquid food. These findings suggest novel roles for antagonistic AgRP and POMC neurons in the regulation of feeding behaviors across multiple timescales. DOI: http://dx.doi.org/10.7554/eLife.07122.001 eLife Sciences Publications, Ltd 2015-07-10 /pmc/articles/PMC4498165/ /pubmed/26159614 http://dx.doi.org/10.7554/eLife.07122 Text en © 2015, Mandelblat-Cerf et al 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
Mandelblat-Cerf, Yael
Ramesh, Rohan N
Burgess, Christian R
Patella, Paola
Yang, Zongfang
Lowell, Bradford B
Andermann, Mark L
Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title_full Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title_fullStr Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title_full_unstemmed Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title_short Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
title_sort arcuate hypothalamic agrp and putative pomc neurons show opposite changes in spiking across multiple timescales
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498165/
https://www.ncbi.nlm.nih.gov/pubmed/26159614
http://dx.doi.org/10.7554/eLife.07122
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