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Cholinergic neurons in the dorsomedial hypothalamus regulate food intake

OBJECTIVE: Central cholinergic neural circuits play a role in the regulation of feeding behavior. The dorsomedial hypothalamus (DMH) is considered the appetite-stimulating center and contains cholinergic neurons. Here, we study the role of DMH cholinergic neurons in the control of food intake. METHO...

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Autores principales: Jeong, Jae Hoon, Lee, Dong Kun, Jo, Young-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323886/
https://www.ncbi.nlm.nih.gov/pubmed/28271037
http://dx.doi.org/10.1016/j.molmet.2017.01.001
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author Jeong, Jae Hoon
Lee, Dong Kun
Jo, Young-Hwan
author_facet Jeong, Jae Hoon
Lee, Dong Kun
Jo, Young-Hwan
author_sort Jeong, Jae Hoon
collection PubMed
description OBJECTIVE: Central cholinergic neural circuits play a role in the regulation of feeding behavior. The dorsomedial hypothalamus (DMH) is considered the appetite-stimulating center and contains cholinergic neurons. Here, we study the role of DMH cholinergic neurons in the control of food intake. METHODS: To selectively stimulate DMH cholinergic neurons, we expressed stimulatory designer receptors exclusively activated by designer drugs (DREADDs) and channelrhodopsins in DMH cholinergic neurons by injection of adeno-associated virus (AAV) vectors into the DMH of choline acetyltransferase (ChAT)-IRES-Cre mice. We also generated transgenic mice expressing channelrhodopsins in cholinergic neurons with the Cre-LoxP technique. To delete the Chat gene exclusively in the DMH, we injected an AAV carrying a Cre recombinase transgene into the DMH of floxed ChAT mice. Food intake was measured with and without selective stimulation of DMH cholinergic neurons. RESULTS: Mice lacking the Chat gene in the DMH show reduced body weight as compared to control. Chemogenetic activation of DMH cholinergic neurons promotes food intake. This orexigenic effect is further supported by experiments of optogenetic stimulation of DMH cholinergic neurons. DMH cholinergic neurons innervate pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus (ARC). Treatment with acetylcholine (ACh) enhances GABAergic inhibitory transmission to ARC POMC neurons that is blocked by the muscarinic receptor antagonist. Direct activation of cholinergic fibers in the ARC readily stimulates food intake that is also abolished by the muscarinic receptor antagonist. CONCLUSION: ACh released from DMH cholinergic neurons regulates food intake and body weight. This effect is mediated in part through regulation of ARC POMC neurons. Activation of muscarinic receptors on GABAergic axon terminals enhances inhibitory tone to ARC POMC neurons. Hence, this novel DMH(ACh) → ARC(POMC) pathway plays an important role in the control of food intake and body weight.
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spelling pubmed-53238862017-03-07 Cholinergic neurons in the dorsomedial hypothalamus regulate food intake Jeong, Jae Hoon Lee, Dong Kun Jo, Young-Hwan Mol Metab Brief Communication OBJECTIVE: Central cholinergic neural circuits play a role in the regulation of feeding behavior. The dorsomedial hypothalamus (DMH) is considered the appetite-stimulating center and contains cholinergic neurons. Here, we study the role of DMH cholinergic neurons in the control of food intake. METHODS: To selectively stimulate DMH cholinergic neurons, we expressed stimulatory designer receptors exclusively activated by designer drugs (DREADDs) and channelrhodopsins in DMH cholinergic neurons by injection of adeno-associated virus (AAV) vectors into the DMH of choline acetyltransferase (ChAT)-IRES-Cre mice. We also generated transgenic mice expressing channelrhodopsins in cholinergic neurons with the Cre-LoxP technique. To delete the Chat gene exclusively in the DMH, we injected an AAV carrying a Cre recombinase transgene into the DMH of floxed ChAT mice. Food intake was measured with and without selective stimulation of DMH cholinergic neurons. RESULTS: Mice lacking the Chat gene in the DMH show reduced body weight as compared to control. Chemogenetic activation of DMH cholinergic neurons promotes food intake. This orexigenic effect is further supported by experiments of optogenetic stimulation of DMH cholinergic neurons. DMH cholinergic neurons innervate pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus (ARC). Treatment with acetylcholine (ACh) enhances GABAergic inhibitory transmission to ARC POMC neurons that is blocked by the muscarinic receptor antagonist. Direct activation of cholinergic fibers in the ARC readily stimulates food intake that is also abolished by the muscarinic receptor antagonist. CONCLUSION: ACh released from DMH cholinergic neurons regulates food intake and body weight. This effect is mediated in part through regulation of ARC POMC neurons. Activation of muscarinic receptors on GABAergic axon terminals enhances inhibitory tone to ARC POMC neurons. Hence, this novel DMH(ACh) → ARC(POMC) pathway plays an important role in the control of food intake and body weight. Elsevier 2017-01-12 /pmc/articles/PMC5323886/ /pubmed/28271037 http://dx.doi.org/10.1016/j.molmet.2017.01.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Brief Communication
Jeong, Jae Hoon
Lee, Dong Kun
Jo, Young-Hwan
Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title_full Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title_fullStr Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title_full_unstemmed Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title_short Cholinergic neurons in the dorsomedial hypothalamus regulate food intake
title_sort cholinergic neurons in the dorsomedial hypothalamus regulate food intake
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323886/
https://www.ncbi.nlm.nih.gov/pubmed/28271037
http://dx.doi.org/10.1016/j.molmet.2017.01.001
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