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High-fat feeding disrupts daily eating behavior rhythms in obesity-prone but not in obesity-resistant male inbred mouse strains

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Abnormal meal timing, like skipping breakfast and late-night snacking, is associated with obesity in humans. Disruption of daily eating rhythms also contributes to obesity in mice. When fed a high-fat diet, male C57BL/6J mice have disrupted eating behavior rhythms and they become obese. In contrast to obesity-prone C57BL/6J mice, some inbred strains of mice are resistant to high-fat diet-induced obesity. In this study, we sought to determine whether there are distinct effects of high-fat feeding on daily eating behavior rhythms in obesity-prone and obesity-resistant male mice. Male obesity-prone (C57BL/6J and 129X1/SvJ) and obesity-resistant (SWR/J and BALB/cJ) mice were fed low-fat diet or high-fat diet for 6 wk. Consistent with previous studies, obesity-prone male mice gained more weight and adiposity during high-fat diet feeding than obesity-resistant male mice. The amplitude of the daily rhythm of eating behavior was markedly attenuated in male obesity-prone mice fed high-fat diet, but not in obesity-resistant males. In contrast, high-fat feeding did not differentially affect locomotor activity rhythms in obesity-prone and obesity-resistant male mice. Together, these data suggest that regulation of the daily rhythm of eating may underlie the propensity to develop diet-induced obesity in male mice.

Original languageEnglish
Pages (from-to)R619-R629
JournalAmerican Journal of Physiology - Regulatory Integrative and Comparative Physiology
Volume320
Issue number5
DOIs
StatePublished - Apr 2021

Bibliographical note

Publisher Copyright:
© 2021 the American Physiological Society

Funding

This research was funded by National Institutes of Health (NIH) Grants K01DK098321 (to J.S.P.), the Washington University Diabetes Research Center P30DK020579 (Pilot Award to J.S.P.), P30GM127211, the National Center for Advancing Translational Sciences UL1TR001998, as well as the Gertrude F. Ribble Grant (to O.O. and J.M.C), the American Physiological Society Undergraduate Summer Research Fellowship (to J.D.L.), and the University of Kentucky.

FundersFunder number
National Institutes of Health (NIH)K01DK098321
National Institutes of Health (NIH)
American Physiological Society
National Center for Advancing Translational Sciences (NCATS)UL1TR001998
National Center for Advancing Translational Sciences (NCATS)
University of Kentucky
Washington University Diabetes Research and Training CenterP30GM127211, P30DK020579
Washington University Diabetes Research and Training Center

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Circadian
    • Eating behavior rhythm
    • High-fat diet
    • Mouse
    • Obesity

    ASJC Scopus subject areas

    • General Medicine

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