4.8 Article

Distinct Circadian Signatures in Liver and Gut Clocks Revealed by Ketogenic Diet

Journal

CELL METABOLISM
Volume 26, Issue 3, Pages 523-+

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2017.08.015

Keywords

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Funding

  1. NIH [DA036408]
  2. Institute National de la Sante et de la Recherche Medicale (INSERM, France) [INSERM-44790]
  3. Novo Nordisk Foundation Challenge Grant [NNF-202585]
  4. Japan Foundation for Pediatric Research [13-003]
  5. Sumitomo Life Welfare and Culture Foundation
  6. EMBO ALTF [1510-2012]
  7. Human Frontiers Science Program LT [000576/2013]

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The circadian clock orchestrates rhythms in physiology and behavior, allowing organismal adaptation to daily environmental changes. While food intake profoundly influences diurnal rhythms in the liver, how nutritional challenges are differentially interpreted by distinct tissue-specific clocks remains poorly explored. Ketogenic diet (KD) is considered to have metabolic and therapeutic value, though its impact on circadian homeostasis is virtually unknown. We show that KD has profound and differential effects on liver and intestine clocks. Specifically, the amplitude of clock-controlled genes and BMAL1 chromatin recruitment are drastically altered by KD in the liver, but not in the intestine. KD induces nuclear accumulation of PPAR alpha in both tissues but with different circadian phase. Also, gut and liver clocks respond differently to carbohydrate supplementation to KD. Importantly, KD induces serum and intestinal beta-hydroxyl-butyrate levels to robustly oscillate in a circadian manner, an event coupled to tissue-specific cyclic histone deacetylase (HDAC) activity and histone acetylation.

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