PMID- 35032416 OWN - NLM STAT- MEDLINE DCOM- 20220214 LR - 20220214 IS - 1530-6860 (Electronic) IS - 0892-6638 (Linking) VI - 36 IP - 2 DP - 2022 Feb TI - Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal muscle. PG - e22133 LID - 10.1096/fj.202100707R [doi] AB - Shift-workers show an increased incidence of type 2 diabetes mellitus (T2DM). A possible mechanism is the disruption of the circadian timing of glucose homeostasis. Skeletal muscle mitochondrial function is modulated by the molecular clock. We used time-restricted feeding (TRF) during the inactive phase to investigate how mistimed feeding affects muscle mitochondrial metabolism. Rats on an ad libitum (AL) diet were compared to those that could eat only during the light (inactive) or dark (active) phase. Mitochondrial respiration, metabolic gene expressions, and metabolite concentrations were determined in the soleus muscle. Rats on AL feeding or dark-fed TRF showed a clear daily rhythm in muscle mitochondrial respiration. This rhythm in mitochondrial oxidative phosphorylation capacity was abolished in light-fed TRF animals and overall 24h respiration was lower. The expression of several genes involved in mitochondrial biogenesis and the fission/fusion machinery was altered in light-fed animals. Metabolomics analysis indicated that light-fed animals had lost rhythmic levels of alpha-ketoglutarate and citric acid. Contrastingly, lipidomics showed that light-fed animals abundantly gained rhythmicity in levels of triglycerides. Furthermore, while the RER shifted entirely with the food intake in the light-fed animals, many measured metabolic parameters (e.g., activity and mitochondrial respiration) did not strictly align with the shifted timing of food intake, resulting in a mismatch between expected metabolic supply/demand (as dictated by the circadian timing system and light/dark-cycle) and the actual metabolic supply/demand (as dictated by the timing of food intake). These data suggest that shift-work impairs mitochondrial metabolism and causes metabolic inflexibility, which can predispose to T2DM. CI - (c) 2022 The Authors. The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology. FAU - de Goede, Paul AU - de Goede P AUID- ORCID: 0000-0003-4489-7422 AD - Laboratory of Endocrinology, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Hypothalamic Integration Mechanisms Group, Netherlands Institute for Neuroscience (NIN), an Institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands. FAU - Wust, Rob C I AU - Wust RCI AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Laboratory for Myology, Department of Human Movement Sciences, Faculty of Behavioural and Movement Sciences, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. FAU - Schomakers, Bauke V AU - Schomakers BV AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Core Facility Metabolomics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Denis, Simone AU - Denis S AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Vaz, Frederic M AU - Vaz FM AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Core Facility Metabolomics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Pras-Raves, Mia L AU - Pras-Raves ML AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Core Facility Metabolomics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - van Weeghel, Michel AU - van Weeghel M AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Core Facility Metabolomics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Yi, Chun-Xia AU - Yi CX AD - Laboratory of Endocrinology, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Department of Endocrinology and Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Kalsbeek, Andries AU - Kalsbeek A AUID- ORCID: 0000-0001-9606-8453 AD - Laboratory of Endocrinology, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. AD - Hypothalamic Integration Mechanisms Group, Netherlands Institute for Neuroscience (NIN), an Institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands. AD - Department of Endocrinology and Metabolism, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. FAU - Houtkooper, Riekelt H AU - Houtkooper RH AD - Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - FASEB J JT - FASEB journal : official publication of the Federation of American Societies for Experimental Biology JID - 8804484 SB - IM MH - Animals MH - Cell Respiration/*physiology MH - Circadian Clocks/*physiology MH - Circadian Rhythm/*physiology MH - Diabetes Mellitus, Type 2/physiopathology MH - Diet/methods MH - Eating/physiology MH - Energy Metabolism/physiology MH - Fasting/*physiology MH - Feeding Behavior/physiology MH - Gene Expression/physiology MH - Male MH - Mitochondria/*physiology MH - Muscle, Skeletal/*physiology MH - Organelle Biogenesis MH - Oxidative Phosphorylation MH - Photoperiod MH - Rats MH - Rats, Wistar OTO - NOTNLM OT - lipidomics OT - metabolomics OT - mitochondrial respiration OT - soleus muscle OT - time-restricted feeding EDAT- 2022/01/16 06:00 MHDA- 2022/02/15 06:00 CRDT- 2022/01/15 17:05 PHST- 2021/11/26 00:00 [revised] PHST- 2021/04/28 00:00 [received] PHST- 2021/12/17 00:00 [accepted] PHST- 2022/01/15 17:05 [entrez] PHST- 2022/01/16 06:00 [pubmed] PHST- 2022/02/15 06:00 [medline] AID - 10.1096/fj.202100707R [doi] PST - ppublish SO - FASEB J. 2022 Feb;36(2):e22133. doi: 10.1096/fj.202100707R.