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Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency.

Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Research Abstract Details 

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  • Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Abstract Text:

    eric p zorrillaEric P Zorrilla,manuel sanchez-alavezManuel Sanchez-Alavez,shuei sugamaShuei Sugama,molly brennanMolly Brennan,rosette fernandezRosette Fernandez,tamas bartfaiTamas Bartfai,bruno contiBruno Conti,eric p zorrillaEric P Zorrilla,manuel sanchez-alavezManuel Sanchez-Alavez,shuei sugamaShuei Sugama,molly brennanMolly Brennan,rosette fernandezRosette Fernandez,tamas bartfaiTamas Bartfai,bruno contiBruno Conti,

    Circulating levels of the cytokine interleukin 18 (IL-18) are elevated in obesity. Here, we show that administration of IL-18 suppresses appetite, feed efficiency, and weight regain in food-deprived male and female C57BL/6J mice. Intraperitoneal vs. intracerebroventricular routes of IL-18 administration had similar potency and did not promote formation of a conditioned taste aversion (malaise-like behavior). Mice partially (Il18(+/-)) or totally (Il18(-/-)) deficient in IL-18 were hyperphagic by young adulthood, with null mutants then becoming overweight by the fifth month of life. Adult Il18(-/-) mice gained 2- to 3-fold more weight than WT mice per unit energy consumed of low- or high-fat diet. Indirect calorimetry revealed reduced energy expenditure in female Il18(-/-) mice and increased respiratory exchange ratios [volume of carbon dioxide production (VCO(2))/volume of oxygen consumption (VO(2))] in mutants of both sexes. Hyperphagia continued in maturity, with overeating greatest during the mid- to late-dark cycle. Relative white fat-pad mass of Il18(-/-) mice was approximately 2- to 3-fold greater than that of WT, with gonadal, mesenteric, and inguinal depots growing most. The data suggest that endogenous IL-18 signaling modulates food intake, metabolism, and adiposity during adulthood and might be a central or peripheral pharmacological target for controlling energy homeostasis.

    Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Publishing Authors By Initials

    ep zorrillaEP Zorrilla,m sanchez-alavezM Sanchez-Alavez,s sugamaS Sugama,m brennanM Brennan,r fernandezR Fernandez,t bartfaiT Bartfai,b contiB Conti,ep zorrillaEP Zorrilla,m sanchez-alavezM Sanchez-Alavez,s sugamaS Sugama,m brennanM Brennan,r fernandezR Fernandez,t bartfaiT Bartfai,b contiB Conti,

    For similar abstracts research abstracts see: abstracts research

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    Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Proceedings of the National Academy of Sciences of

    VOLUME: 104

    Page Numbers: 11097-102

    Journal Abbreviation: Proc. Natl. Acad. Sci. U.S.A.

    ISSN: 1091-6490

    DAY: 19

    MONTH: 06

    YEAR: 2007

    Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505876

    Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency. Keywords Mesh Terms:

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    Grant and Affiliation Information for Interleukin-18 controls energy homeostasis by suppressing appetite and feed efficiency.

    AFFILIATION: Harold L. Dorris Neurological Research Institute, Committee on the Neurobiology of Addictive Disorders, and Molecular and Integrative Neurosciences Department, The Scripps Research Institute, La Jolla, CA 92037, USA. ezorrilla@scripps.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States PHS

    GRANT: P30N5057096

    ACRONYM: NS

    MEDLINETA: Proc Natl Acad Sci U S A

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