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Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice.

Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Research Abstract Details 

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  • Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Abstract Text:

    elizabeth p newberryElizabeth P Newberry,yan xieYan Xie,susan m kennedySusan M Kennedy,jianyang luoJianyang Luo,nicholas o davidsonNicholas O Davidson,

    Liver fatty acid-binding protein (L-Fabp) regulates murine hepatic fatty acid trafficking in response to fasting. In this study, we show that L-Fabp(-/-) mice fed a high-fat Western diet for up to 18 weeks are less obese and accumulate less hepatic triglyceride than C57BL/6J controls. Paradoxically, both control and L-Fabp(-/-) mice manifested comparable glucose intolerance and insulin resistance when fed a Western diet. Protection against obesity in Western diet-fed L-Fabp(-/-) mice was not due to discernable changes in food intake, fat malabsorption, or heat production, although intestinal lipid secretion kinetics were significantly slower in both chow-fed and Western diet-fed L-Fabp(-/-) mice. By contrast, there was a significant increase in the respiratory exchange ratio in L-Fabp(-/-) mice, suggesting a shift in energy substrate use from fat to carbohydrate, findings supported by an approximately threefold increase in serum lactate. Microarray analysis revealed increased expression of genes involved in lipid synthesis (fatty acid synthase, squalene epoxidase, hydroxy-methylglutaryl coenzyme A reductase), while genes involved in glycolysis (glucokinase and glycerol kinase) were decreased in L-Fabp(-/-) mice. Fatty acid synthase expression was also increased in the skeletal muscle of L-Fabp(-/-) mice. In conclusion, L-Fabp may function as a metabolic sensor in regulating lipid homeostasis. We suggest that L-Fabp(-/-) mice are protected against Western diet-induced obesity and hepatic steatosis through a series of adaptations in both hepatic and extrahepatic energy substrate use. (HEPATOLOGY 2006;44:1191-1205.).

    Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Publishing Authors By Initials

    ep newberryEP Newberry,y xieY Xie,sm kennedySM Kennedy,j luoJ Luo,no davidsonNO Davidson,

    For similar nucleic acids, nucleotides, and nucleosides: nucleic acids: rna: rna, messenger research abstracts see: nucleic acids, nucleotides, and nucleosides: nucleic acids: rna: rna, messenger research

    PUBMED ID PMID:

    MEDLINE DATE:

    Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Hepatology (Baltimore, Md.)

    VOLUME: 44

    Page Numbers: 1191-205

    Journal Abbreviation: Hepatology

    ISSN: 0270-9139

    DAY: 3

    MONTH: Nov

    YEAR: 2006

    Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8302946

    Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Keywords Mesh Terms:

    KEYWORDS: RNA, Messenger

    MESH TERMS: analysis

    Chemical & Substance for Abstract: Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice. Information

    Substance Name: Fatty Acid Synthetase Complex

    Registry Number: EC 6.-

    Grant and Affiliation Information for Protection against Western diet-induced obesity and hepatic steatosis in liver fatty acid-binding protein knockout mice.

    AFFILIATION: Division of Gastroenterology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63105, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL-38180

    ACRONYM: HL

    MEDLINETA: Hepatology

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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