An adipokine feedback regulating diurnal food intake rhythms in mice.
Anthony H TsangChristiane E KochJana-Thabea KiehnCosima X SchmidtHenrik OsterPublished in: eLife (2020)
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). Adipoq-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 via AdipoR1-mediated upregulation of the core clock gene Bmal1. 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.
Keyphrases
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- long non coding rna
- metabolic syndrome
- atrial fibrillation
- dna methylation
- genome wide identification
- gene expression
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- transcription factor
- big data
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- machine learning
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- single cell
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- fluorescent probe
- high fat diet induced
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- case control
- genome wide analysis