VGluT3 BNST neurons transmit GABA and restrict sucrose consumption

Objective: The bed nucleus of the stria terminalis (BNST) is involved in feeding, reward, aversion, and anxiety-like behavior. We identify BNST neurons defined by the expression of vesicular glutamate transporter 3, VGluT3. Methods: A combination of in situ hybridization, tract tracing, ex vivo whol...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Molecular Metabolism
المؤلفون الرئيسيون: Annie Ly, Rachel Karnosky, Emily D. Prévost, Hayden Hotchkiss, Julianne M. Pelletier, Robert L. Spencer, Christopher P. Ford, David H. Root
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Elsevier 2025-08-01
الموضوعات:
الوصول للمادة أونلاين:http://www.sciencedirect.com/science/article/pii/S2212877825000857
_version_ 1849471788931612672
author Annie Ly
Rachel Karnosky
Emily D. Prévost
Hayden Hotchkiss
Julianne M. Pelletier
Robert L. Spencer
Christopher P. Ford
David H. Root
author_facet Annie Ly
Rachel Karnosky
Emily D. Prévost
Hayden Hotchkiss
Julianne M. Pelletier
Robert L. Spencer
Christopher P. Ford
David H. Root
author_sort Annie Ly
collection DOAJ
container_title Molecular Metabolism
description Objective: The bed nucleus of the stria terminalis (BNST) is involved in feeding, reward, aversion, and anxiety-like behavior. We identify BNST neurons defined by the expression of vesicular glutamate transporter 3, VGluT3. Methods: A combination of in situ hybridization, tract tracing, ex vivo whole-cell electrophysiology, in vivo recording, optogenetic, and behavioral approaches were used. Results: VGluT3 neurons were localized to anteromedial BNST, were molecularly distinct from accumbal VGluT3 neurons, and co-express vesicular GABA transporter (VGaT). BNST VGluT3 neurons projected to arcuate nucleus (ARC) and paraventricular nucleus of the hypothalamus (PVN), regions critical for feeding and homeostatic regulation. Most single BNST VGluT3 neurons projected to either PVN or ARC and a subset projected to both. BNST VGluT3 neurons functionally transmit GABA to both ARC and PVN, with rare glutamate co-transmission to ARC. In vivo, VGluT3 BNST neurons showed greater neuronal activity in response to sucrose consumption while sated compared with fasted. When fasted, optogenetic stimulation of BNST VGluT3 neurons decreased sucrose consumption using several stimulation conditions but not when stimulation occurred prior to sucrose access, suggesting that BNST VGluT3 activation concurrent with consumption in the fasted state reduces feeding. BNST VGluT3 activation had no effect on anxiety-like behavior in several paradigms (novelty-suppressed feeding, open field, and elevated zero maze). BNST VGluT3 activation also did not result in real-time place preference or aversion. Conclusions: We interpret these data such that VGluT3 BNST neurons represent a unique cellular population within the BNST that provides inhibitory input to hypothalamic regions to decrease sucrose consumption.
format Article
id doaj-art-e3bf23d54b5e4f54a10edffb50c18a28
institution Directory of Open Access Journals
issn 2212-8778
language English
publishDate 2025-08-01
publisher Elsevier
record_format Article
spelling doaj-art-e3bf23d54b5e4f54a10edffb50c18a282025-08-20T03:17:24ZengElsevierMolecular Metabolism2212-87782025-08-019810217810.1016/j.molmet.2025.102178VGluT3 BNST neurons transmit GABA and restrict sucrose consumptionAnnie Ly0Rachel Karnosky1Emily D. Prévost2Hayden Hotchkiss3Julianne M. Pelletier4Robert L. Spencer5Christopher P. Ford6David H. Root7Department of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USADepartment of Pharmacology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, 80045, USADepartment of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Pl, Boulder, CO, 80301, USA; Corresponding author. Boettcher Investigator, Department of Psychology and Neuroscience, University of Colorado Boulder, 2860 Wilderness Place, Boulder, CO, 80301, USA.Objective: The bed nucleus of the stria terminalis (BNST) is involved in feeding, reward, aversion, and anxiety-like behavior. We identify BNST neurons defined by the expression of vesicular glutamate transporter 3, VGluT3. Methods: A combination of in situ hybridization, tract tracing, ex vivo whole-cell electrophysiology, in vivo recording, optogenetic, and behavioral approaches were used. Results: VGluT3 neurons were localized to anteromedial BNST, were molecularly distinct from accumbal VGluT3 neurons, and co-express vesicular GABA transporter (VGaT). BNST VGluT3 neurons projected to arcuate nucleus (ARC) and paraventricular nucleus of the hypothalamus (PVN), regions critical for feeding and homeostatic regulation. Most single BNST VGluT3 neurons projected to either PVN or ARC and a subset projected to both. BNST VGluT3 neurons functionally transmit GABA to both ARC and PVN, with rare glutamate co-transmission to ARC. In vivo, VGluT3 BNST neurons showed greater neuronal activity in response to sucrose consumption while sated compared with fasted. When fasted, optogenetic stimulation of BNST VGluT3 neurons decreased sucrose consumption using several stimulation conditions but not when stimulation occurred prior to sucrose access, suggesting that BNST VGluT3 activation concurrent with consumption in the fasted state reduces feeding. BNST VGluT3 activation had no effect on anxiety-like behavior in several paradigms (novelty-suppressed feeding, open field, and elevated zero maze). BNST VGluT3 activation also did not result in real-time place preference or aversion. Conclusions: We interpret these data such that VGluT3 BNST neurons represent a unique cellular population within the BNST that provides inhibitory input to hypothalamic regions to decrease sucrose consumption.http://www.sciencedirect.com/science/article/pii/S2212877825000857VGluT3FeedingGABAGlutamateInternal stateCo-transmission
spellingShingle Annie Ly
Rachel Karnosky
Emily D. Prévost
Hayden Hotchkiss
Julianne M. Pelletier
Robert L. Spencer
Christopher P. Ford
David H. Root
VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
VGluT3
Feeding
GABA
Glutamate
Internal state
Co-transmission
title VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
title_full VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
title_fullStr VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
title_full_unstemmed VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
title_short VGluT3 BNST neurons transmit GABA and restrict sucrose consumption
title_sort vglut3 bnst neurons transmit gaba and restrict sucrose consumption
topic VGluT3
Feeding
GABA
Glutamate
Internal state
Co-transmission
url http://www.sciencedirect.com/science/article/pii/S2212877825000857
work_keys_str_mv AT anniely vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT rachelkarnosky vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT emilydprevost vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT haydenhotchkiss vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT juliannempelletier vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT robertlspencer vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT christopherpford vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption
AT davidhroot vglut3bnstneuronstransmitgabaandrestrictsucroseconsumption