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GLP-1 Neurons in the Nucleus of the Solitary Tract Project Directly to the Ventral Tegmental Area and Nucleus Accumbens to Control for Food Intake
Open accessAbstract
Central glucagon-like-peptide-1 (GLP-1) receptor activation reduces food intake; however, brain nuclei and mechanism(s) mediating this effect remain poorly understood. Although central nervous system GLP-1 is produced almost exclusively in the nucleus of the solitary tract in the hindbrain, GLP-1 receptors (GLP-1R) are expressed throughout the brain, including nuclei in the mesolimbic reward system (MRS), e.g. the ventral tegmental area (VTA) and the nucleus accumbens (NAc). Here, we examine the MRS as a potential site of action for GLP-1-mediated control of food intake and body weight. Double immunohistochemistry for Fluorogold (monosynaptic retrograde tracer) and GLP-1 neuron immunoreactivity indicated that GLP-1-producing nucleus tractus solitarius neurons project directly to the VTA, the NAc core, and the NAc shell. Pharmacological data showed that GLP-1R activation in the VTA, NAc core, and NAc shell decreased food intake, especially of highly-palatable foods, and body weight. Moreover, blockade of endogenous GLP-1R signaling in the VTA and NAc core resulted in a significant increase in food intake, establishing a physiological relevance for GLP-1 signaling in the MRS. Current data highlight these nuclei within the MRS as novel sites for GLP-1R-mediated control of food intake and body weight.
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“neurons in the VTA and/or NAc express GLP-1 (24,25), ghrelin (26,27), leptin (28,29), insulin (30), orexin (31) and melanocortin receptors (32).”
From Obesity and addiction: Neurobiological overlaps (2013) · cites this paper as [24]
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“Moreover, neurons in VTA and/or nucleus accumbens (NAc) express glucagon-like peptide-1 (11,12), ghrelin (13,14), leptin (15,16), insulin (17), orexin (18), and melanocortin receptors (19).”
From The Addictive Dimensionality of Obesity (2013) · cites this paper as [11]
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Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Biology of Incretins: GLP-1 and GIP
Baggio, L. L., & Drucker, D. J. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.03.054 · Cited by 3,639
The Physiology of Glucagon-like Peptide 1
Holst, J. J. (2007) · Physiological Reviews · doi:10.1152/physrev.00034.2006 · Cited by 3,371
A role for glucagon-like peptide-1 in the central regulation of feeding
Turton, M. D., O'Shea, D., Gunn, I., Beak, S. A., Edwards, C. M. B., Meeran, K., Choi, S. J., Taylor, G. M., Heath, M. M., Lambert, P. D., et al. (1996) · Nature · doi:10.1038/379069a0 · Cited by 1,950
Buse, J. B., Rosenstock, J., Sesti, G., Schmidt, W. E., Montanya, E., Brett, J. H., Zychma, M., & Blonde, L. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60659-0 · Cited by 1,503
Buse, J. B., Henry, R. R., Han, J., Kim, D. D., Fineman, M. S., Baron, A. D., & for the Exenatide-113 Clinical Study Group (2004) · Diabetes Care · doi:10.2337/diacare.27.11.2628 · Cited by 1,346
Astrup, A., Rössner, S., Van Gaal, L., Rissanen, A., Niskanen, L., Al Hakim, M., Madsen, J., Rasmussen, M. F., & Lean, M. E. (2009) · The Lancet · doi:10.1016/s0140-6736(09)61375-1 · Cited by 1,163
Wise, R. A. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80079-1 · Cited by 1,072
Conditioned Aversion to Saccharin Resulting from Exposure to Gamma Radiation
García, J., Kimeldorf, D. J., & Koelling, R. A. (1955) · Science · doi:10.1126/science.122.3160.157 · Cited by 1,011
Leptin Receptor Signaling in Midbrain Dopamine Neurons Regulates Feeding
Hommel, J. D., Trinko, R., Sears, R. M., Georgescu, D., Liu, Z.-W., Gao, X.-B., Thurmon, J. J., Marinelli, M., & DiLeone, R. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.023 · Cited by 902
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- Hayes, 2011, Intracellular signals mediating the food intake suppressive effects of hindbrain glucagon-like-peptide-1 receptor activation., Cell Metab, 13, 320, 10.1016/j.cmet.2011.02.001 · DOI
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Sorted by citations
Items 201–300 of 516
The emerging role of glucagon-like peptide 1 in binge eating
Balantekin, K. N., Kretz, M. J., & Mietlicki-Baase, E. G. (2024) · Journal of Endocrinology · doi:10.1530/joe-23-0405 · Cited by 38
GLP-1 neurons form a local synaptic circuit within the rodent nucleus of the solitary tract
Card, J. P., Johnson, A. L., Llewellyn‐Smith, I. J., Zheng, H., Anand, R., Brierley, D. I., Trapp, S., & Rinaman, L. (2018) · Journal of Comparative Neurology · doi:10.1002/cne.24482 · Cited by 38
Falk, S., Petersen, J., Svendsen, C., Leguizamón, C. R. R., Jørgensen, S. H., Krauth, N., Ludwig, M. Q., Lundø, K., Roostalu, U., Skovbjerg, G., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112466 · Cited by 38
Keel, P. K., Bodell, L. P., Forney, K. J., Appelbaum, J., & Williams, D. L. (2019) · Physiology & Behavior · doi:10.1016/j.physbeh.2019.112565 · Cited by 38
Jensen, M. E., Galli, A., Thomsen, M., Jensen, K. L., Thomsen, G. K., Klausen, M. K., Vilsbøll, T., Christensen, M., Holst, J. J., Owens, A. W., et al. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104772 · Cited by 42
Dixon, T. N., McNally, G. P., & Ong, Z. Y. (2020) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.14437 · Cited by 38
Gut peptide regulation of food intake - evidence for the modulation of hedonic feeding.
Woodward, O. R. M., Gribble, F. M., Reimann, F. M., & Lewis, J. E. (2021) · Apollo (University of Cambridge) · doi:10.17863/cam.74301 · Cited by 38
Urbanik, L. A., Acharya, N., & Grigson, P. S. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.08.023 · Cited by 39
High-fat diet changes the temporal profile of GLP-1 receptor-mediated hypophagia in rats
Mul, J. D., Begg, D. P., Barrera, J. G., Li, B., Matter, E. K., D’Alessio, D. A., Woods, S. C., Seeley, R. J., & Sandoval, D. A. (2013) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00588.2012 · Cited by 38
Rupprecht, L. E., Mietlicki‐Baase, E. G., Zimmer, D. J., McGrath, L. E., Olivos, D. R., & Hayes, M. R. (2013) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00367.2013 · Cited by 37
Self-citationEvans, B., Stoltzfus, B., Acharya, N., Nyland, J. E., Arnold, A. C., Freet, C. S., Bunce, S. C., & Grigson, P. S. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.08.022 · Cited by 39
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Perazza, F., Leoni, L., Colosimo, S., Musio, A., Bocedi, G., D’Avino, M., Agnelli, G., Nicastri, A., Rossetti, C., Sacilotto, F., et al. (2024) · Metabolites · doi:10.3390/metabo14040186 · Cited by 39
Distribution of glucagon-like peptide 1-immunopositive neurons in human caudal medulla
Zheng, H., Cai, L., & Rinaman, L. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0714-z · Cited by 36
Knudsen, L. B., Secher, A., Hecksher‐Sørensen, J., & Pyke, C. (2016) · Journal of Diabetes Investigation · doi:10.1111/jdi.12463 · Cited by 38
Functional, Diagnostic and Therapeutic Aspects of Gastrointestinal Hormones
Ahmed∥, M., & Ahmed, S. (2019) · Gastroenterology Research · doi:10.14740/gr1219 · Cited by 36
Development and validation of the Food Noise Questionnaire
Diktas, H. E., Cardel, M. I., Foster, G. D., LeBlanc, M. M., Dickinson, S. L., Ables, E. M., Chen, X., Nathan, R., Shapiro, D., & Martin, C. K. (2025) · Obesity · doi:10.1002/oby.24216 · Cited by 35
Moving beyond energy homeostasis: New roles for glucagon-like peptide-1 in food and drug reward
Reddy, I. A., Stanwood, G. D., & Galli, A. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.10.003 · Cited by 36
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Jonghe, B. C. D., Holland, R. A., Olivos, D. R., Rupprecht, L. E., Kanoski, S. E., & Hayes, M. R. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.10.031 · Cited by 35
Self-citationAllingbjerg, M.-L., Hansen, S. N., Secher, A., & Thomsen, M. (2022) · Experimental and Clinical Psychopharmacology · doi:10.1037/pha0000620 · Cited by 34
Bae, J. H., Choi, H. J., Cho, K. I. K., Kim, L. K., Kwon, J. S., & Cho, Y. M. (2020) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2019.0018 · Cited by 33
Tufvesson‐Alm, M., Shevchouk, O. T., & Jerlhag, E. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.1092828 · Cited by 33
Central Control of Feeding Behavior by the Secretin, PACAP, and Glucagon Family of Peptides
Sekar, R., Wang, L., & Chow, B. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00018 · Cited by 33
Howell, E., Baumgartner, H. M., Zallar, L. J., Selva, J. A., Engel, L., & Currie, P. J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040889 · Cited by 33
What is bipolar disorder? A disease model of dysregulated energy expenditure
Mansur, R. B., Lee, Y. L., McIntyre, R. S., & Brietzke, E. M. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.006 · Cited by 33
Milano, W., Biasio, V. D., Munzio, W. D., Foggia, G., & Capasso, A. (2020) · Endocrine Metabolic & Immune Disorders - Drug Targets · doi:10.2174/1871530320666200515112853 · Cited by 33
Effects of Glucagon-like peptide 1 (GLP-1) analogs in the hippocampus
Diz-Chaves, Y., Herrera-Pérez, S., González-Matías, L. C., & Mallo, F. (2022) · Vitamins and hormones · doi:10.1016/bs.vh.2021.12.005 · Cited by 33
Sasaki, T. (2017) · Nutrients · doi:10.3390/nu9101151 · Cited by 35
Brain Feeding Circuits after Roux-en-Y Gastric Bypass
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Fortin, S. M., Chen, J. C., Petticord, M. C., Ragozzino, F. J., Peters, J. H., & Hayes, M. R. (2023) · Science Advances · doi:10.1126/sciadv.adh0980 · Cited by 32
Self-citationFarokhnia, M., Fede, S. J., Grodin, E. N., Browning, B. D., Crozier, M. E., Schwandt, M. L., Hodgkinson, C. A., Momenan, R., & Leggio, L. (2022) · Scientific Reports · doi:10.1038/s41598-022-17190-3 · Cited by 32
Shi, L., Zhu, J., Yang, P., Tang, X., Yu, W., Pan, C., Shen, M., Zhu, D., Cheng, J., & Ye, X. (2017) · Obesity Research & Clinical Practice · doi:10.1016/j.orcp.2017.01.003 · Cited by 31
Wang, L., Sui, L., Panigrahi, S. K., Meece, K., Xin, Y., Kim, J., Gromada, J., Doege, C. A., Wardlaw, S. L., Egli, D. M., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.12.021 · Cited by 33
Friedrich, T., Schalla, M. A., Scharner, S., Kühne, S. G., Goebel‐Stengel, M., Kobelt, P., Rose, M., & Stengel, A. (2019) · Brain Research · doi:10.1016/j.brainres.2019.03.034 · Cited by 32
Targeting the intestinal L-cell for obesity and type 2 diabetes treatment
Albrechtsen, N. J. W., Kuhre, R. E., Deacon, C. F., & Holst, J. J. (2013) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2014.862152 · Cited by 32
You, Z., Wang, B., Gardner, E. L., & Wise, R. A. (2018) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2018.11.001 · Cited by 31
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Giannakogeorgou, A., & Roden, M. (2024) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.17848 · Cited by 30
Wen, S., Nguyen, T., Gong, M., Yuan, X., Wang, C., Jin, J., & Zhou, L. (2021) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s312527 · Cited by 34
Li, Y., & Rosenblit, P. D. (2018) · Current Cardiology Reports · doi:10.1007/s11886-018-1051-2 · Cited by 30
The diverse effects of brain glucagon‐like peptide 1 receptors on ingestive behaviour
Williams, D. L. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15535 · Cited by 32
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Sirohi, S., Cleef, A. V., & Davis, J. F. (2016) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2016.12.009 · Cited by 28
Roberts, C. A., Christiansen, P., & Halford, J. C. G. (2017) · Acta Diabetologica · doi:10.1007/s00592-017-0994-x · Cited by 28
Converging vulnerability factors for compulsive food and drug use
Serafine, K. M., O’Dell, L. E., & Zorrilla, E. P. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108556 · Cited by 29
Andresen, M. C., Fawley, J. A., & Hofmann, M. E. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00191 · Cited by 30
Glucagon‐like peptide‐1 drives energy metabolism on the synaptic highway
Liu, J., & Pang, Z. P. (2016) · FEBS Journal · doi:10.1111/febs.13785 · Cited by 27
Kreisler, A. D., & Rinaman, L. (2016) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00243.2015 · Cited by 27
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Décarie-Spain, L., Fisette, A., Zhu, Z., Yang, B., DiMarchi, R. D., Tschöp, M. H., Finan, B., Fulton, S., & Clemmensen, C. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.03.035 · Cited by 27
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Liang, N.-C., Bello, N. T., & Moran, T. H. (2012) · International Journal of Obesity · doi:10.1038/ijo.2012.16 · Cited by 27
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Vestlund, J., & Jerlhag, E. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.104687 · Cited by 31
Dunigan, A. I., & Roseberry, A. G. (2022) · Addiction Neuroscience · doi:10.1016/j.addicn.2022.100011 · Cited by 28
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Fernandes, M. F., Sharma, S., Hryhorczuk, C., Auguste, S., & Fulton, S. (2013) · Canadian Journal of Diabetes · doi:10.1016/j.jcjd.2013.04.004 · Cited by 27
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Burcelin, R., Gourdy, P., & Dalle, S. (2014) · Physiology · doi:10.1152/physiol.00009.2013 · Cited by 26
Chometton, S., Charrière, K., Bayer, L., Houdayer, C., Franchi, G., Poncet, F., FELLMANN, D., & Risold, P. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1353-3 · Cited by 29
Kokkinos, A. D., Tsilingiris, D., le Roux, C. W., Rubino, F., & Mantzoros, C. S. (2019) · Metabolism · doi:10.1016/j.metabol.2019.153960 · Cited by 28
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Liu, D., Tang, Q., Wang, D., Song, S.-P., Yang, X.-N., Hu, S.-W., Wang, Z.-Y., Xu, Z., Liu, H., Yang, J., et al. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0713-0 · Cited by 27
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Jin, R., Sun, S., Hu, Y., Zhang, H., & Sun, X. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03954-4 · Cited by 26
Gut-brain peptides in corticostriatal-limbic circuitry and alcohol use disorders
Vadnie, C. A., Park, J. H., Gawad, N. A., Ho, A. M., Hinton, D. J., & Choi, D. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00288 · Cited by 26
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Surówka, A. D., Krygowska‐Wajs, A., Ziomber, A., Thor, P. J., Chrobak, A. A., & Szczerbowska‐Boruchowska, M. (2015) · NeuroMolecular Medicine · doi:10.1007/s12017-015-8349-7 · Cited by 24
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Sasaki, T., Matsui, S., & Kitamura, T. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17071081 · Cited by 27
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Alves, G. A. M., Teranishi, M., Ortega, A. C. T. D. C. G., James, F., & Arachchige, A. S. P. M. (2025) · Medical Sciences · doi:10.3390/medsci13030136 · Cited by 32
Vestlund, J., & Jerlhag, E. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104778 · Cited by 27
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Passeri, A., Municchi, D., Cavalieri, G., Babicola, L., Ventura, R., & Segni, M. D. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1240748 · Cited by 32
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Nicze, M., Dec, A., Borówka, M., Krzyżak, D., Bołdys, A., Bułdak, Ł., & Okopień, B. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158202 · Cited by 30
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Klausen, M. K., Knudsen, G. M., Vilsbøll, T., & Fink‐Jensen, A. (2025) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.70004 · Cited by 26
GLP-1 physiology and pharmacology along the gut-brain axis
Beutler, L. R. (2026) · Journal of Clinical Investigation · doi:10.1172/jci194744 · Cited by 28
Olbrich, H., Kridin, K., Zirpel, H., Hernández, G., Sadik, C. D., Gaffal, E., Thaçi, D., & Ludwig, R. J. (2025) · British Journal of Dermatology · doi:10.1093/bjd/ljaf346 · Cited by 22
Bernosky‐Smith, K. A., Stanger, D. B., Trujillo, A. J., Mitchell, L. R., España, R. A., & Bass, C. E. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.12.007 · Cited by 21
Yammine, L., Kosten, T. R., Pimenova, M., & Schmitz, J. M. (2019) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2019.01.033 · Cited by 23
Pierce-Messick, Z. J., & Pratt, W. E. (2020) · Neuroreport · doi:10.1097/wnr.0000000000001545 · Cited by 22
Maejima, Y., Yokota, S., Shimizu, M., Horita, S., Kobayashi, D., Hazama, A., & Shimomura, K. (2021) · Nutrition & Metabolism · doi:10.1186/s12986-021-00582-z · Cited by 21
Eren, C. Y., Kara, B., Sancak, S., Uysal, S. P., Yazıcı, D., Okuroğlu, N., Whitton, A. E., Rutherford, A. V., & Eser, H. Y. (2021) · Journal of Clinical Psychopharmacology · doi:10.1097/jcp.0000000000001409 · Cited by 21
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Tasyurek, H. M., Altunbaş, H., Canatan, H., Griffith, T. S., & Şanlıoğlu, S. (2014) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2014.7 · Cited by 22
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Moran, T. H., & Ladenheim, E. E. (2016) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.07.009 · Cited by 22
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Rozo, A., Babu, D., Suen, P.-M. A., Groff, D., Seeley, R., Simmons, R., Seale, P., Ahima, R., & Stoffers, D. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.05.006 · Cited by 19
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Schalla, M. A., Taché, Y., & Stengel, A. (2021) · Comprehensive physiology · doi:10.1002/cphy.c200007 · Cited by 28
Novelle, M. G., & Diéguez, C. (2018) · European Eating Disorders Review · doi:10.1002/erv.2641 · Cited by 22
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Kern, K. A., & Mietlicki‐Baase, E. G. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112958 · Cited by 20
Listos, J., Listos, P., Baranowska‐Bosiacka, I., Karpiuk, A., Filarowska, J., Łupina, M., Słowik, T., Zawiślak, S., & Kotlinska, J. H. (2022) · Molecules · doi:10.3390/molecules27082478 · Cited by 21
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Brutman, J. N., SIROHI, S. K., & Davis, J. F. (2019) · Current Psychiatry Reports · doi:10.1007/s11920-019-1084-2 · Cited by 20
Łupina, M., Talarek, S., Kotlinska, J. H., Gibuła‐Tarłowska, E., Listos, P., & Listos, J. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104616 · Cited by 21
Mella, R., Schmidt, C. B., Romagnoli, P. P., Teske, J. A., & Perez‐Leighton, C. E. (2017) · Obesity · doi:10.1002/oby.21939 · Cited by 19
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Metadata
- Authors
- Alhadeff, A. L., Rupprecht, L. E., & Hayes, M. R.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Hayes, Matthew R.
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 2012-02-01
- Volume
- 153
- Issue
- 2
- Pages
- 647-658
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- PMC
- PMC3275387
- OpenAlex
- W2140625608
- Cited by
- 515
- References
- 69
- Citations by year
- 2026: 66 · 2025: 45 · 2024: 38 · 2023: 26 · 2022: 33 · 2021: 36 · 2020: 33 · 2019: 34 · 2018: 25 · 2017: 28 · 2016: 34 · 2015: 31 · 2014: 34 · 2013: 37 · 2012: 13
- FWCI
- 12.59
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Endocrinology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Pennsylvania
- National Institutes of Health
- U.S. Public Health Service (NIDDK 085435)
- National Institute of Diabetes and Digestive and Kidney Diseases (K01DK085435)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- glucagon-like peptide-1, GLP-1 receptor, nucleus tractus solitarius, ventral tegmental area, nucleus accumbens, mesolimbic reward system, food intake regulation, body weight, palatable food, monosynaptic projection, hindbrain neurons
- MeSH terms
- Glucagon-Like Peptide-1 Receptor, Exenatide, Animals, Dose-Response Relationship, Drug, Eating, Gene Expression Regulation, Hypoglycemic Agents, Male, Neurons, Nucleus Accumbens, Peptides, Venoms, Signal Transduction, Rats, Sprague-Dawley, Solitary Nucleus, Ventral Tegmental Area, Receptors, Glucagon, Rats, Glucagon-Like Peptide 1
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