Adipocyte NADH dehydrogenase reverses circadian and diet-induced metabolic syndrome

Circadian clocks are internal timing systems that enable organisms to anticipate and adapt to daily environmental changes. These rhythms arise from a transcription-translation feedback loop in which CLOCK and BMAL1 regulate the expression of thousands of genes, including their repressors PER and CRY. Disruption of circadian rhythms contributes to obesity, metabolic disease and cancer, yet how the clock maintains metabolic homeostasis remains limited. Here we report that the clock regulates oxidative metabolism in adipocytes through diurnal complex I respiration. Disrupting the clock in male mice via adipocyte-specific genetic deletion or high-fat-diet feeding reduces complex I respiration in adipocytes, leading to suppression of the peroxisome proliferator-activated receptor and insulin signalling pathways. In contrast, restoring complex I function by expressing yeast NDI1 in adipocytes protects against diet-induced and circadian-induced metabolic dysfunction independently of weight gain. These findings reveal that adipocyte circadian disruption impairs metabolic health through mitochondrial complex I dysfunction, establishing clock control of complex I as a key regulator of metabolic homeostasis.

Authors

Institutions

Publication Details

Journal
Nature Metabolism
Published
2026-02-18
DOI
https://doi.org/10.1038/s42255-026-01464-5
Citations
1
Primary Topic
Circadian rhythm and melatonin
Type
article
Field-Weighted Citation Impact
25.88

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Adipocyte NADH dehydrogenase reverses circadian and diet-induced metabolic syndrome

Chelsea Hepler, Clara Bien Peek, Jonathan Cedernaes, Biliana Marcheva et al.
1 citations
Nature Metabolism
Circadian rhythm and melatonin
25.88
article

Adipocyte NADH dehydrogenase reverses circadian and diet-induced metabolic syndrome

Chelsea Hepler, Clara Bien Peek, Jonathan Cedernaes, Biliana Marcheva, Benjamin J. Weidemann, Jacqueline Hecker, Colleen R. Reczek, Navdeep S. Chandel, Nathan J. Waldeck, Y. E. Chen, Kathryn Moynihan Ramsey, Ziming Zhu, Joseph J. Bass, Rino Nozawa, Anneke K. Thorne, Grant D. Barish, Joseph V. Mastroni
article en
1 citations

Abstract

Circadian clocks are internal timing systems that enable organisms to anticipate and adapt to daily environmental changes. These rhythms arise from a transcription-translation feedback loop in which CLOCK and BMAL1 regulate the expression of thousands of genes, including their repressors PER and CRY. Disruption of circadian rhythms contributes to obesity, metabolic disease and cancer, yet how the clock maintains metabolic homeostasis remains limited. Here we report that the clock regulates oxidative metabolism in adipocytes through diurnal complex I respiration. Disrupting the clock in male mice via adipocyte-specific genetic deletion or high-fat-diet feeding reduces complex I respiration in adipocytes, leading to suppression of the peroxisome proliferator-activated receptor and insulin signalling pathways. In contrast, restoring complex I function by expressing yeast NDI1 in adipocytes protects against diet-induced and circadian-induced metabolic dysfunction independently of weight gain. These findings reveal that adipocyte circadian disruption impairs metabolic health through mitochondrial complex I dysfunction, establishing clock control of complex I as a key regulator of metabolic homeostasis.

Nature MetabolismVol. 8(3)
Northwestern University (US), University of Michigan (US), Michigan Medicine (US)
American Diabetes Association, U.S. Department of Veterans Affairs, Northwestern University, National Institutes of Health, Robert H. Lurie Comprehensive Cancer Center, National Institute on Aging, National Heart, Lung, and Blood Institute, National Cancer Institute, National Institute of Diabetes and Digestive and Kidney Diseases
Openalex Percentile: Top 1%
Circadian rhythm and melatonin
25.88
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.