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...
| الحاوية / القاعدة: | Molecular Metabolism |
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| المؤلفون الرئيسيون: | , , , , , , , |
| التنسيق: | مقال |
| اللغة: | الإنجليزية |
| منشور في: |
Elsevier
2025-08-01
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| الموضوعات: | |
| الوصول للمادة أونلاين: | http://www.sciencedirect.com/science/article/pii/S2212877825000857 |
| _version_ | 1849471788931612672 |
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| 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 |
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