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Glucagon-like peptide-1 analog liraglutide leads to multiple metabolic alterations in diet-induced obese mice
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Title
Glucagon-like peptide-1 analog liraglutide leads to multiple metabolic alterations in diet-induced obese mice
Issued Date
2022-12
Citation
Park, S. (2022-12). Glucagon-like peptide-1 analog liraglutide leads to multiple metabolic alterations in diet-induced obese mice. Journal of Biological Chemistry, 298(12). doi: 10.1016/j.jbc.2022.102682
Type
Article
Author Keywords
diabeteshypothalamusliraglutidelivermetabolomicsobesityplasmaskeletal muscle
Keywords
WEIGHT-LOSSGLUCOSE-HOMEOSTASISINSULIN-RESISTANCERECEPTOR AGONISTARCUATE NUCLEUSACIDHYPOTHALAMUSACTIVATIONSIGNATUREEXCRETION
ISSN
0021-9258
Abstract
Liraglutide, a glucagon-like peptide-1 analog, has beneficial metabolic effects in patients with type 2 diabetes and obesity. Although the high efficacy of liraglutide as an anti-diabetic and anti-obesity drug is well known, liraglutide-induced metabolic alterations in diverse tissues remain largely unexplored. Here, we report the changes in metabolic profiles induced by a 2-week subcutaneous injection of liraglutide in diet-induced obese mice fed a high-fat diet for 8 weeks. Our comprehensive metabolomic analyses of the hypothalamus, plasma, liver, and skeletal muscle showed that liraglutide intervention led to various metabolic alterations in comparison with diet-induced obese or nonobese mice. We found that liraglutide remarkably coordinated not only fatty acid metabolism in the hypothalamus and skeletal muscle but also amino acid and carbohydrate metabolism in plasma and liver. Comparative analyses of metabolite dynamics revealed that liraglutide rewired intertissue metabolic correlations. Our study points to a previously unappreciated metabolic alteration by liraglutide in several tissues, which may underlie its therapeutic effects within and across the tissues. © 2022 The Authors
URI
http://hdl.handle.net/20.500.11750/17357
DOI
10.1016/j.jbc.2022.102682
Publisher
American Society for Biochemistry and Molecular Biology Inc.
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Kim, Eun-Kyoung김은경

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