Glucagon-Like Peptide-1-Responsive Catecholamine Neurons in the Area Postrema Link Peripheral Glucagon-Like Peptide-1 with Central Autonomic Control Sites

التفاصيل البيبلوغرافية
العنوان: Glucagon-Like Peptide-1-Responsive Catecholamine Neurons in the Area Postrema Link Peripheral Glucagon-Like Peptide-1 with Central Autonomic Control Sites
المؤلفون: Hiroshi Yamamoto, Hui Fang, Charlotte E. Lee, Anthony N. Hollenberg, Brian Choi, Joel K. Elmquist, Daniel J. Drucker, Toshiro Kishi
بيانات النشر: Society for Neuroscience, 2003.
سنة النشر: 2003
مصطلحات موضوعية: Central Nervous System, Male, Transcriptional Activation, medicine.medical_specialty, endocrine system, Tyrosine 3-Monooxygenase, Neuropeptide, Biology, Blood–brain barrier, Glucagon-Like Peptide-1 Receptor, Cell Line, Rats, Sprague-Dawley, Catecholamines, Glucagon-Like Peptide 1, Internal medicine, medicine, Receptors, Glucagon, Solitary Nucleus, Animals, Autonomic Pathways, RNA, Messenger, ARTICLE, Protein Precursors, In Situ Hybridization, Neurons, Gastric emptying, Tyrosine hydroxylase, Venoms, General Neuroscience, Area postrema, digestive, oral, and skin physiology, Solitary tract, Glucagon, Glucagon-like peptide-1, Immunohistochemistry, Peptide Fragments, Rats, medicine.anatomical_structure, Endocrinology, Area Postrema, Catecholamine, Exenatide, Peptides, hormones, hormone substitutes, and hormone antagonists, medicine.drug
الوصف: Glucagon-like peptide-1 (GLP-1) released from the gut is an incretin that stimulates insulin secretion. GLP-1 is also a brain neuropeptide that has diverse central actions, including inhibition of food and water intake, gastric emptying, and stimulation of neuroendocrine responses characteristic of visceral illness. Both intravenous and intracerebroventricular administration of GLP-1 receptor (GLP-1R) agonists increase blood pressure and heart rate and induce Fos-like immunoreactivity (Fos-IR) in autonomic regulatory sites in the rat brain. The area postrema (AP) is a circumventricular organ and has been implicated in processing visceral sensory information. GLP-1Rs are densely expressed in the AP, and peripheral GLP-1R agonists induce Fos-IR in AP neurons to a greater degree than intracerebroventricular administration. Because the AP lacks a blood–brain barrier, we hypothesized that the AP is a key site for peripheral GLP-1 to activate central autonomic regulatory sites. In this study, we found that many tyrosine hydroxylase (TH)-containing neurons in the AP expressed GLP-1Rs and Fos-IR after intravenous GLP-1R agonists. Furthermore, intravenous but not intracerebroventricular GLP-1R agonists inducedTHtranscription in the APin vivo. In addition, GLP-1R agonists directly activatedTHtranscription in anin vitrocell system. Finally, we found that GLP-1-responsive TH neurons in the AP innervate autonomic control sites, including the parabrachial nucleus, nucleus of solitary tract, and ventrolateral medulla. These findings suggest that catecholamine neurons in the AP link peripheral GLP-1 and central autonomic control sites that mediate the diverse neuroendocrine and autonomic actions of peripheral GLP-1.
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::466f3bbb4d88eb8ee8333745a2ffcc6fTest
https://europepmc.org/articles/PMC6742071Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....466f3bbb4d88eb8ee8333745a2ffcc6f
قاعدة البيانات: OpenAIRE