TY - JOUR
T1 - Day-night rhythm of skeletal muscle metabolism is disturbed in older, metabolically compromised individuals
AU - Wefers, Jakob
AU - Connell, Niels J.
AU - Fealy, Ciaran E.
AU - Andriessen, Charlotte
AU - de Wit, Vera
AU - van Moorsel, Dirk
AU - Moonen-Kornips, Esther
AU - Jorgensen, Johanna A.
AU - Hesselink, Matthijs K. C.
AU - Havekes, Bas
AU - Hoeks, Joris
AU - Schrauwen, Patrick
N1 - Funding Information:
We thank the research volunteers for their participation. This work is partly financed by the Netherlands Organization for Scientific Research (TOP 40-00812-98-14047 to P.S.). We acknowledge the support from the Netherlands Cardiovascular Research Initiative: an initiative with support of the Dutch Heart Foundation (CVON2014-02 ENERGISE). J. Hoeks is supported by a Vidi Grant (917.14.358) for innovative research from the Netherlands Organization for Scientific Research (NWO) and a Senior Fellowship from the Dutch Diabetes Research Foundation (grant number 2013.82.1639).
Funding Information:
We thank the research volunteers for their participation. This work is partly financed by the Netherlands Organization for Scientific Research (TOP 40-00812-98-14047 to P.S.). We acknowledge the support from the Netherlands Cardiovascular Research Initiative: an initiative with support of the Dutch Heart Foundation (CVON2014-02 ENERGISE). J. Hoeks is supported by a Vidi Grant (917.14.358) for innovative research from the Netherlands Organization for Scientific Research ( NWO ) and a Senior Fellowship from the Dutch Diabetes Research Foundation (grant number 2013.82.1639 ).
Publisher Copyright:
© 2020 The Author(s)
PY - 2020/11
Y1 - 2020/11
N2 - Objective: Skeletal muscle mitochondrial function and energy metabolism displays day-night rhythmicity in healthy, young individuals. Twenty-four-hour rhythmicity of metabolism has been implicated in the etiology of age-related metabolic disorders. Whether day-night rhythmicity in skeletal muscle mitochondrial function and energy metabolism is altered in older, metabolically comprised humans remains unknown.Methods: Twelve male overweight volunteers with impaired glucose tolerance and insulin sensitivity stayed in a metabolic research unit for 2 days under free living conditions with regular meals. Indirect calorimetry was performed at 5 time points (8 AM, 1 PM, 6 PM, 11 PM, 4 AM), followed by a muscle biopsy. Mitochondrial oxidative capacity was measured in permeabilized muscle fibers using high-resolution respirometry.Results: Mitochondrial oxidative capacity did not display rhythmicity. The expression of circadian core clock genes BMAL1 and REV-ERB alpha showed a clear day-night rhythm (p <0.001), peaking at the end of the waking period. Remarkably, the repressor clock gene PER2 did not show rhythmicity, whereas PER1 and PER3 were strongly rhythmic (p <0.001). On the whole-body level, resting energy expenditure was highest in the late evening (p <0.001). Respiratory exchange ratio did not decrease during the night, indicating metabolic inflexibility.Conclusions: Mitochondrial oxidative capacity does not show a day-night rhythm in older, overweight participants with impaired glucose tolerance and insulin sensitivity. In addition, gene expression of PER2 in skeletal muscle indicates that rhythmicity of the negative feedback loop of the molecular clock is disturbed. (C) 2020 The Authors. Published by Elsevier GmbH.
AB - Objective: Skeletal muscle mitochondrial function and energy metabolism displays day-night rhythmicity in healthy, young individuals. Twenty-four-hour rhythmicity of metabolism has been implicated in the etiology of age-related metabolic disorders. Whether day-night rhythmicity in skeletal muscle mitochondrial function and energy metabolism is altered in older, metabolically comprised humans remains unknown.Methods: Twelve male overweight volunteers with impaired glucose tolerance and insulin sensitivity stayed in a metabolic research unit for 2 days under free living conditions with regular meals. Indirect calorimetry was performed at 5 time points (8 AM, 1 PM, 6 PM, 11 PM, 4 AM), followed by a muscle biopsy. Mitochondrial oxidative capacity was measured in permeabilized muscle fibers using high-resolution respirometry.Results: Mitochondrial oxidative capacity did not display rhythmicity. The expression of circadian core clock genes BMAL1 and REV-ERB alpha showed a clear day-night rhythm (p <0.001), peaking at the end of the waking period. Remarkably, the repressor clock gene PER2 did not show rhythmicity, whereas PER1 and PER3 were strongly rhythmic (p <0.001). On the whole-body level, resting energy expenditure was highest in the late evening (p <0.001). Respiratory exchange ratio did not decrease during the night, indicating metabolic inflexibility.Conclusions: Mitochondrial oxidative capacity does not show a day-night rhythm in older, overweight participants with impaired glucose tolerance and insulin sensitivity. In addition, gene expression of PER2 in skeletal muscle indicates that rhythmicity of the negative feedback loop of the molecular clock is disturbed. (C) 2020 The Authors. Published by Elsevier GmbH.
KW - Mitochondria
KW - Skeletal muscle
KW - Day-night rhythm
KW - Insulin resistance
KW - ORAL GLUCOSE-TOLERANCE
KW - MITOCHONDRIAL DYSFUNCTION
KW - OBESITY
KW - DYNAMICS
KW - BASAL
U2 - 10.1016/j.molmet.2020.101050
DO - 10.1016/j.molmet.2020.101050
M3 - Article
C2 - 32659272
SN - 2212-8778
VL - 41
JO - Molecular Metabolism
JF - Molecular Metabolism
M1 - 101050
ER -