Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons

Objective: Leptin modulates food reward via central leptin receptor (LepRb) expressing neurons. Food reward requires stimulation of midbrain dopamine neurons and is modulated by central leptin action, but the exact central mechanisms remain unclear. Stimulatory and inhibitory leptin actions on dopam...

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Main Authors: Amanda Laque, Sangho Yu, Emily Qualls-Creekmore, Sarah Gettys, Candice Schwartzenburg, Kelly Bui, Christopher Rhodes, Hans-Rudolf Berthoud, Christopher D. Morrison, Brenda K. Richards, Heike Münzberg
Format: Article
Language:English
Published: Elsevier 2015-10-01
Series:Molecular Metabolism
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Online Access:http://www.sciencedirect.com/science/article/pii/S2212877815001362
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spelling doaj-eb81a303401f451eb6b1bef3078a984d2020-11-25T02:30:40ZengElsevierMolecular Metabolism2212-87782015-10-0141070671710.1016/j.molmet.2015.07.002Leptin modulates nutrient reward via inhibitory galanin action on orexin neuronsAmanda Laque0Sangho Yu1Emily Qualls-Creekmore2Sarah Gettys3Candice Schwartzenburg4Kelly Bui5Christopher Rhodes6Hans-Rudolf Berthoud7Christopher D. Morrison8Brenda K. Richards9Heike Münzberg10Central Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USAKovler Diabetes Center, University of Chicago, Chicago, IL, USANeurobiology of Nutrition Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USANeurosignaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USAGenetics of Eating Behavior Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USACentral Leptin Signaling Laboratory, Pennington Biomedical Research Center, LSU System, Baton Rouge, LA, USAObjective: Leptin modulates food reward via central leptin receptor (LepRb) expressing neurons. Food reward requires stimulation of midbrain dopamine neurons and is modulated by central leptin action, but the exact central mechanisms remain unclear. Stimulatory and inhibitory leptin actions on dopamine neurons have been reported, e.g. by indirect actions on orexin neurons or via direct innervation of dopamine neurons in the ventral tegmental area. Methods: We showed earlier that LepRb neurons in the lateral hypothalamus (LHA) co-express the inhibitory acting neuropeptide galanin (GAL-LepRb neurons). We studied the involvement of GAL-LepRb neurons to regulate nutrient reward in mice with selective LepRb deletion from galanin neurons (GAL-LepRbKO mice). Results: We found that the rewarding value and preference for sucrose over fat was increased in GAL-LepRbKO mice compared to controls. LHA GAL-LepRb neurons innervate orexin neurons, but not the VTA. Further, expression of galanin and its receptor GalR1 are decreased in the LHA of GAL-LepRbKO mice, resulting in increased activation of orexin neurons. Conclusion: We suggest galanin as an important mediator of leptin action to modulate nutrient reward by inhibiting orexin neurons.http://www.sciencedirect.com/science/article/pii/S2212877815001362SucroseIntralipidIncentive runwayLateral hypothalamusLocus coeruleusTwo-bottle choice
collection DOAJ
language English
format Article
sources DOAJ
author Amanda Laque
Sangho Yu
Emily Qualls-Creekmore
Sarah Gettys
Candice Schwartzenburg
Kelly Bui
Christopher Rhodes
Hans-Rudolf Berthoud
Christopher D. Morrison
Brenda K. Richards
Heike Münzberg
spellingShingle Amanda Laque
Sangho Yu
Emily Qualls-Creekmore
Sarah Gettys
Candice Schwartzenburg
Kelly Bui
Christopher Rhodes
Hans-Rudolf Berthoud
Christopher D. Morrison
Brenda K. Richards
Heike Münzberg
Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
Molecular Metabolism
Sucrose
Intralipid
Incentive runway
Lateral hypothalamus
Locus coeruleus
Two-bottle choice
author_facet Amanda Laque
Sangho Yu
Emily Qualls-Creekmore
Sarah Gettys
Candice Schwartzenburg
Kelly Bui
Christopher Rhodes
Hans-Rudolf Berthoud
Christopher D. Morrison
Brenda K. Richards
Heike Münzberg
author_sort Amanda Laque
title Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
title_short Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
title_full Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
title_fullStr Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
title_full_unstemmed Leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
title_sort leptin modulates nutrient reward via inhibitory galanin action on orexin neurons
publisher Elsevier
series Molecular Metabolism
issn 2212-8778
publishDate 2015-10-01
description Objective: Leptin modulates food reward via central leptin receptor (LepRb) expressing neurons. Food reward requires stimulation of midbrain dopamine neurons and is modulated by central leptin action, but the exact central mechanisms remain unclear. Stimulatory and inhibitory leptin actions on dopamine neurons have been reported, e.g. by indirect actions on orexin neurons or via direct innervation of dopamine neurons in the ventral tegmental area. Methods: We showed earlier that LepRb neurons in the lateral hypothalamus (LHA) co-express the inhibitory acting neuropeptide galanin (GAL-LepRb neurons). We studied the involvement of GAL-LepRb neurons to regulate nutrient reward in mice with selective LepRb deletion from galanin neurons (GAL-LepRbKO mice). Results: We found that the rewarding value and preference for sucrose over fat was increased in GAL-LepRbKO mice compared to controls. LHA GAL-LepRb neurons innervate orexin neurons, but not the VTA. Further, expression of galanin and its receptor GalR1 are decreased in the LHA of GAL-LepRbKO mice, resulting in increased activation of orexin neurons. Conclusion: We suggest galanin as an important mediator of leptin action to modulate nutrient reward by inhibiting orexin neurons.
topic Sucrose
Intralipid
Incentive runway
Lateral hypothalamus
Locus coeruleus
Two-bottle choice
url http://www.sciencedirect.com/science/article/pii/S2212877815001362
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