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The effects of liraglutide in mice with diet-induced obesity studied by metabolomics

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    SYSNO ASEP0474423
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleThe effects of liraglutide in mice with diet-induced obesity studied by metabolomics
    Author(s) Bugáňová, M. (CZ)
    Pelantová, H. (CZ)
    Holubová, M. (CZ)
    Šedivá, B. (CZ)
    Maletínská, L. (CZ)
    Železná, B. (CZ)
    Kuneš, Jaroslav (FGU-C) RID, ORCID
    Kačer, P. (CZ)
    Kuzma, M. (CZ)
    Haluzík, M. (CZ)
    Source TitleJournal of Endocrinology. - : BioScientifica - ISSN 0022-0795
    Roč. 233, č. 1 (2017), s. 93-104
    Number of pages12 s.
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsNMR metabolomics ; obesity type 2 ; diabetes mellitus ; liraglutide ; mouse urine
    Subject RIVFB - Endocrinology, Diabetology, Metabolism, Nutrition
    OECD categoryEndocrinology and metabolism (including diabetes, hormones)
    Institutional supportFGU-C - RVO:67985823
    UT WOS000397242300012
    EID SCOPUS85015671351
    DOI10.1530/JOE-16-0478
    AnnotationLiraglutide is the glucagon-like peptide-1 receptor agonist widely used for the treatment of type 2 diabetes mellitus. Recently, it has been demonstrated to decrease cardiovascular morbidity and mortality in patients with type 2 diabetes and high cardiovascular risk. Although the major modes of liraglutide action are well-known, its detailed action at the metabolic level has not been studied. To this end, we explored the effect of 2-week liraglutide treatment in C57BL/6 male mice with obesity and diabetes induced by 13 weeks of high-fat diet using NMR spectroscopy to capture the changes in urine metabolic profile induced by the therapy. The liraglutide treatment decreased body and fat pads weight along with blood glucose and triglyceride levels. NMR spectroscopy identified 11 metabolites significantly affected by liraglutide treatment as compared to high-fat diet-fed control group. These metabolites included ones involved in nicotinamide adenine dinucleotide metabolism, beta-oxidation of fatty acids and microbiome changes. Although majority of the metabolites changed after liraglutide treatment were similar as the ones previously identified after vildagliptin administration in a similar mouse model, the changes in creatinine, taurine and trigonelline were specific for liraglutide administration. The significance of these changes and its possible use in the personalization of antidiabetic therapy in humans requires further research.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2018
Number of the records: 1  

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