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

التفاصيل البيبلوغرافية
العنوان: 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
المؤلفون: Laura E. Rupprecht, Matthew R. Hayes, Amber L. Alhadeff
المصدر: Endocrinology. 153:647-658
بيانات النشر: The Endocrine Society, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Male, endocrine system, medicine.medical_specialty, Central nervous system, Nucleus accumbens, Biology, Glucagon-Like Peptide-1 Receptor, Nucleus Accumbens, Rats, Sprague-Dawley, Eating, Endocrinology, Glucagon-Like Peptide 1, Internal medicine, Receptors, Glucagon, Solitary Nucleus, medicine, Animals, Hypoglycemic Agents, Neurons, Dose-Response Relationship, Drug, Venoms, Energy Balance-Obesity, Solitary nucleus, Ventral Tegmental Area, digestive, oral, and skin physiology, Solitary tract, Glucagon-like peptide-1, Rats, Ventral tegmental area, medicine.anatomical_structure, Gene Expression Regulation, nervous system, Exenatide, Neuron, Peptides, Nucleus, hormones, hormone substitutes, and hormone antagonists, Signal Transduction
الوصف: 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.
تدمد: 1945-7170
0013-7227
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8a48518fe265f91516bb9dc6104ca74Test
https://doi.org/10.1210/en.2011-1443Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....e8a48518fe265f91516bb9dc6104ca74
قاعدة البيانات: OpenAIRE