Glucagon-like Peptide-2 Acts Partially Through Central GLP-2R and MC4R in Mobilizing Stored Lipids from the Intestine

Պահպանված է:
Մատենագիտական մանրամասներ
Հրատարակված է:Nutrients vol. 17, no. 9 (2025), p. 1416
Հիմնական հեղինակ: Mukherjee Kundanika
Այլ հեղինակներ: Khan Muhammad Saad Abdullah, Howland, John G, Xiao Changting
Հրապարակվել է:
MDPI AG
Խորագրեր:
Առցանց հասանելիություն:Citation/Abstract
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024 7 |a 10.3390/nu17091416  |2 doi 
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045 2 |b d20250101  |b d20251231 
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100 1 |a Mukherjee Kundanika 
245 1 |a Glucagon-like Peptide-2 Acts Partially Through Central GLP-2R and MC4R in Mobilizing Stored Lipids from the Intestine 
260 |b MDPI AG  |c 2025 
513 |a Journal Article 
520 3 |a Background: Glucagon-like peptide-2 (GLP-2) is a gut hormone secreted in response to nutrient intake and regulates lipid metabolism in the gut. The present study aims to elucidate the underlying mechanism of GLP-2 in stimulating gut lipid secretion in the fasted state by testing whether GLP-2 signals through the brain’s GLP-2 receptor and melanocortin 4 receptor (MC4R). Methods: Sprague-Dawley rats were implanted with a mesenteric lymph duct cannula for measuring gut lipid secretion and an intracerebroventricular cannula for infusion of a GLP-2R antagonist (GLP-2(11-33)), an MC4R antagonist (SHU9119), or saline as a control. The rat received a lipid infusion into the small intestine and a peritoneal injection of GLP-2 five hours later. Results: Brain administration of a GLP-2R antagonist or an MC4R antagonist attenuated the stimulatory effects of peripheral GLP-2 on lymph triglyceride output. These effects were associated with differential changes in the expression of key genes in jejunal endothelial cells, smooth muscle cells, and neuronal cells. Conclusions: These results support the involvement of central GLP-2R and MC4R in a neural pathway for GLP-2 to mobilize lipids stored in the gut during the post-absorptive state. 
610 4 |a University of Saskatchewan 
651 4 |a St Louis Missouri 
651 4 |a United States--US 
653 |a Software 
653 |a Glucagon 
653 |a Gene expression 
653 |a Peptides 
653 |a Lipids 
653 |a Surgery 
653 |a Animals 
653 |a Catheters 
653 |a Morphology 
653 |a Laboratories 
700 1 |a Khan Muhammad Saad Abdullah 
700 1 |a Howland, John G 
700 1 |a Xiao Changting 
773 0 |t Nutrients  |g vol. 17, no. 9 (2025), p. 1416 
786 0 |d ProQuest  |t Health & Medical Collection 
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856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3203214626/fulltextPDF/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch