An adipokine feedback regulating diurnal food intake rhythms in mice

• Published in: eLife 2020-07, Vol.9
• Main Authors: Tsang, Anthony H, Koch, Christiane E, Kiehn, Jana-Thabea, Schmidt, Cosima X, Oster, Henrik
• Format: Article
• Language: English
• Subjects: Adiponectin; Adiponectin - metabolism; Animals; Appetite; BMAL1 protein; circadian clock; Circadian rhythm; Circadian Rhythm - physiology; Circadian rhythms; Clock gene; Diet; Diurnal; Eating - physiology; Energy; Energy intake; Feedback; Feedback, Physiological; Female; Food; Food intake; Gene expression; Genes; Genetics and Genomics; Hormones; Hypothalamus; Male; Metabolic disorders; Metabolism; Mice - physiology; Mice, Knockout; Neuropeptides; Neuroscience; Physiological aspects; Plasma; Proteins; Risk factors; Transcription
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/eLife.55388

Endogenous circadian clocks have evolved to anticipate 24 hr rhythms in environmental demands. Recent studies suggest that circadian rhythm disruption is a major risk factor for the development of metabolic disorders in humans. Conversely, alterations in energy state can disrupt circadian rhythms of behavior and physiology, creating a vicious circle of metabolic dysfunction. How peripheral energy state affects diurnal food intake, however, is still poorly understood. We here show that the adipokine adiponectin (ADIPOQ) regulates diurnal feeding rhythms through clocks in energy regulatory centers of the mediobasal hypothalamus (MBH). -deficient mice show increased rest phase food intake associated with disrupted transcript rhythms of clock and appetite-regulating genes in the MBH. ADIPOQ regulates MBH clocks AdipoR1-mediated upregulation of the core clock gene . BMAL1, in turn, controls expression of orexigenic neuropeptide expression in the MBH. Together, these data reveal a systemic metabolic circuit to regulate central circadian clocks and energy intake.