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  • Review Article
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Circadian rhythms and exercise — re-setting the clock in metabolic disease

Abstract

Perturbed diurnal rhythms are becoming increasingly evident as deleterious events in the pathology of metabolic diseases. Exercise is well characterized as a crucial intervention in the prevention and treatment of individuals with metabolic diseases. Little is known, however, regarding optimizing the timing of exercise bouts in order to maximize their health benefits. Furthermore, exercise is a potent modulator of skeletal muscle metabolism, and it is clear that skeletal muscle has a strong circadian profile. In humans, mitochondrial function peaks in the late afternoon, and the circadian clock might be inherently impaired in myotubes from patients with metabolic disease. Timing exercise bouts to coordinate with an individual’s circadian rhythms might be an efficacious strategy to optimize the health benefits of exercise. The role of exercise as a Zeitgeber can also be used as a tool in combating metabolic disease. Shift work is known to induce acute insulin resistance, and appropriately timed exercise might improve health markers in shift workers who are at risk of metabolic disease. In this Review, we discuss the literature regarding diurnal skeletal muscle metabolism and the interaction with exercise bouts at different times of the day to combat metabolic disease.

Key points

  • Skeletal muscle has an extensive network of clock-controlled genes, and dysregulation of its molecular clock can lead to deleterious metabolic consequences.

  • Physical strength and skeletal muscle mitochondrial function peak in the late afternoon, whereas low-energy sensitive signalling peaks in the morning.

  • Exercise is a robust Zeitgeber of skeletal muscle clocks, and exercise can reset the molecular circadian clock, thereby effectively ameliorating the negative effects of disrupted sleep patterns.

  • Optimizing the timing of exercise bouts could aid existing therapeutic interventions for the management of metabolic disease.

  • Divergent modalities of exercise can interact with the circadian rhythm, resulting in potent metabolic effects.

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Fig. 1: Skeletal muscle biology and the core clock.
Fig. 2: Human skeletal muscle circadian biology.

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References

  1. Gerhart-Hines, Z. & Lazar, M. A. Circadian metabolism in the light of evolution. Endocr. Rev. 36, 289–304 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Robinson, I. & Reddy, A. B. Molecular mechanisms of the circadian clockwork in mammals. FEBS Lett. 588, 2477–2483 (2014).

    Article  CAS  PubMed  Google Scholar 

  3. Panda, S. Circadian physiology of metabolism. Science 354, 1008–1015 (2016).

    Article  CAS  PubMed  Google Scholar 

  4. Dyar, K. A. et al. Muscle insulin sensitivity and glucose metabolism are controlled by the intrinsic muscle clock. Mol. Metab. 3, 29–41 (2014).

    Article  CAS  PubMed  Google Scholar 

  5. Schiaffino, S., Blaauw, B. & Dyar, K. A. The functional significance of the skeletal muscle clock: lessons from Bmal1 knockout models. Skelet. Muscle 6, 33 (2016).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  6. Vetter, C. et al. Night shift work, genetic risk, and type 2 diabetes in the UK biobank. Diabetes Care 41, 762–769 (2018).

    Article  PubMed  Google Scholar 

  7. Bescos, R. et al. Four days of simulated shift work reduces insulin sensitivity in humans. Acta Physiol. (Oxf.) 223, e13039 (2018).

    Article  CAS  Google Scholar 

  8. Peek, C. B. et al. Circadian clock interaction with HIF1α mediates oxygenic metabolism and anaerobic glycolysis in skeletal muscle. Cell Metab. 25, 86–92 (2017).

    Article  CAS  PubMed  Google Scholar 

  9. Saner, N. J., Bishop, D. J. & Bartlett, J. D. Is exercise a viable therapeutic intervention to mitigate mitochondrial dysfunction and insulin resistance induced by sleep loss? Sleep Med. Rev. 37, 60–68 (2018).

    Article  PubMed  Google Scholar 

  10. Wolff, G. & Esser, K. A. Scheduled exercise phase shifts the circadian clock in skeletal muscle. Med. Sci. Sports Exerc. 44, 1663–1670 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  11. Gabriel, B. M. & Zierath, J. R. The limits of exercise physiology: from performance to health. Cell Metab. 25, 1000–1011 (2017).

    Article  CAS  PubMed  Google Scholar 

  12. Vera, B. et al. Modifiable lifestyle behaviors, but not a genetic risk score, associate with metabolic syndrome in evening chronotypes. Sci. Rep. 8, 945 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  13. Huang, W., Ramsey, K. M., Marcheva, B. & Bass, J. Circadian rhythms, sleep, and metabolism. J. Clin. Invest. 121, 2133–2141 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Atkinson, G., Fullick, S., Grindey, C. & Maclaren, D. Exercise, energy balance and the shift worker. Sports Med. 38, 671–685 (2008).

    Article  PubMed  PubMed Central  Google Scholar 

  15. Patke, A. et al. Mutation of the human circadian clock gene CRY1 in familial delayed sleep phase disorder. Cell 169, 203–215 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Manoogian, E. N. C. & Panda, S. Circadian rhythms, time-restricted feeding, and healthy aging. Ageing Res. Rev. 39, 59–67 (2017).

    Article  PubMed  Google Scholar 

  17. Mure, L. S. et al. Diurnal transcriptome atlas of a primate across major neural and peripheral tissues. Science 359, eaao0318 (2018).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  18. Chtourou, H. & Souissi, N. The effect of training at a specific time of day: a review. J. Strength Cond. Res. 26, 1984–2005 (2012).

    Article  PubMed  Google Scholar 

  19. Driver, H. S. & Taylor, S. R. Exercise and sleep. Sleep Med. Rev. 4, 387–402 (2000).

    Article  PubMed  Google Scholar 

  20. Perrin, L. et al. Transcriptomic analyses reveal rhythmic and CLOCK-driven pathways in human skeletal muscle. eLife 7, e34114 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  21. Dashti, H. S. et al. CRY1 circadian gene variant interacts with carbohydrate intake for insulin resistance in two independent populations: Mediterranean and North American. Chronobiol. Int. 31, 660–667 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Raney, B. J. et al. ENCODE whole-genome data in the UCSC genome browser (2011 update). Nucleic Acids Res. 39, D871–D875 (2011).

    Article  CAS  PubMed  Google Scholar 

  23. Boyle, A. P. et al. Annotation of functional variation in personal genomes using RegulomeDB. Genome Res. 22, 1790–1797 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Villard, J. et al. A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y. Mol. Cell. Biol. 20, 3364–3376 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Dyar, K. A. et al. Transcriptional programming of lipid and amino acid metabolism by the skeletal muscle circadian clock. PLOS Biol. 16, e2005886 (2018).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  26. Lamia, K. A. et al. AMPK regulates the circadian clock by cryptochrome phosphorylation and degradation. Science 326, 437–440 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Um, J. H. et al. Activation of 5′-AMP-activated kinase with diabetes drug metformin induces casein kinase Iepsilon (CKIepsilon)-dependent degradation of clock protein mPer2. J. Biol. Chem. 282, 20794–20798 (2007).

    Article  CAS  PubMed  Google Scholar 

  28. Jordan, S. D. et al. CRY1/2 selectively repress PPARdelta and limit exercise capacity. Cell Metab. 26, 243–255 (2017).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Lowe, M. et al. Cry2 is critical for circadian regulation of myogenic differentiation by Bclaf1-mediated mRNA stabilization of cyclin D1 and Tmem176b. Cell Rep. 22, 2118–2132 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Miller, B. H. et al. Circadian and CLOCK-controlled regulation of the mouse transcriptome and cell proliferation. Proc. Natl Acad. Sci. USA 104, 3342–3347 (2007).

    Article  CAS  PubMed  Google Scholar 

  31. Nakao, R. et al. Atypical expression of circadian clock genes in denervated mouse skeletal muscle. Chronobiol. Int. 32, 486–496 (2015).

    Article  CAS  PubMed  Google Scholar 

  32. Zambon, A. C. et al. Time- and exercise-dependent gene regulation in human skeletal muscle. Genome Biol. 4, R61 (2003).

    Article  PubMed  PubMed Central  Google Scholar 

  33. Hansen, J. et al. Synchronized human skeletal myotubes of lean, obese and type 2 diabetic patients maintain circadian oscillation of clock genes. Sci. Rep. 6, 35047 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. O’Connor, E., Kiely, C., O’Shea, D., Green, S. & Egana, M. Similar level of impairment in exercise performance and oxygen uptake kinetics in middle-aged men and women with type 2 diabetes. Am. J. Physiol. Regul. Integr. Comp. Physiol. 303, R70–R76 (2012).

    Article  PubMed  CAS  Google Scholar 

  35. Phielix, E. & Mensink, M. Type 2 diabetes mellitus and skeletal muscle metabolic function. Physiol. Behav. 94, 252–258 (2008).

    Article  CAS  PubMed  Google Scholar 

  36. van Moorsel, D. et al. Demonstration of a day-night rhythm in human skeletal muscle oxidative capacity. Mol. Metab. 5, 635–645 (2016).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  37. de Goede, P., Wefers, J., Brombacher, E. C., Schrauwen, P. & Kalsbeek, A. Circadian rhythms in mitochondrial respiration. J. Mol. Endocrinol. 60, R115–R130 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  38. Liu, C., Li, S., Liu, T., Borjigin, J. & Lin, J. D. Transcriptional coactivator PGC-1α integrates the mammalian clock and energy metabolism. Nature 447, 477–481 (2007).

    Article  CAS  PubMed  Google Scholar 

  39. Yoon, Y., Galloway, C. A., Jhun, B. S. & Yu, T. Mitochondrial dynamics in diabetes. Antioxid. Redox Signal. 14, 439–457 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Oliva-Ramirez, J., Moreno-Altamirano, M. M., Pineda-Olvera, B., Cauich-Sanchez, P. & Sanchez-Garcia, F. J. Crosstalk between circadian rhythmicity, mitochondrial dynamics and macrophage bactericidal activity. Immunology 143, 490–497 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Schmitt, K. et al. Circadian control of DRP1 activity regulates mitochondrial dynamics and bioenergetics. Cell Metab. 27, 657–666 (2018).

    Article  CAS  PubMed  Google Scholar 

  42. Lassiter, D. G., Sjogren, R. J. O., Gabriel, B. M., Krook, A. & Zierath, J. R. AMPK activation negatively regulates GDAP1, which influences metabolic processes and circadian gene expression in skeletal muscle. Mol. Metab. 16, 12–23 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Xu, Y. et al. Modeling of a human circadian mutation yields insights into clock regulation by PER2. Cell 128, 59–70 (2007).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  44. Zhao, Y. et al. Uncovering the mystery of opposite circadian rhythms between mouse and human leukocytes in humanized mice. Blood 130, 1995–2005 (2017).

    Article  CAS  PubMed  Google Scholar 

  45. Brehm, M. A., Shultz, L. D., Luban, J. & Greiner, D. L. Overcoming current limitations in humanized mouse research. J. Infect. Dis. 208 (Suppl. 2), S125–S130 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Atkinson, G. & Reilly, T. Circadian variation in sports performance. Sports Med. 21, 292–312 (1996).

    Article  CAS  PubMed  Google Scholar 

  47. Facer-Childs, E. & Brandstaetter, R. The impact of circadian phenotype and time since awakening on diurnal performance in athletes. Curr. Biol. 25, 518–522 (2015).

    Article  CAS  PubMed  Google Scholar 

  48. Fowler, P. M. et al. Greater effect of east versus west travel on jet lag, sleep, and team sport performance. Med. Sci. Sports Exerc. 49, 2548–2561 (2017).

    Article  PubMed  Google Scholar 

  49. Facer-Childs, E. & Brandstaetter, R. Circadian phenotype composition is a major predictor of diurnal physical performance in teams. Front. Neurol. 6, 208 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  50. Egan, B. & Zierath, J. R. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 17, 162–184 (2013).

    Article  CAS  PubMed  Google Scholar 

  51. Dyar, K. A. et al. The calcineurin-NFAT pathway controls activity-dependent circadian gene expression in slow skeletal muscle. Mol. Metab. 4, 823–833 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  52. Atkinson, G., Coldwells, A., Reilly, T. & Waterhouse, J. A comparison of circadian rhythms in work performance between physically active and inactive subjects. Ergonomics 36, 273–281 (1993).

    Article  CAS  PubMed  Google Scholar 

  53. Coldwells, A., Atkinson, G. & Reilly, T. Sources of variation in back and leg dynamometry. Ergonomics 37, 79–86 (1994).

    Article  CAS  PubMed  Google Scholar 

  54. Wyse, J. P., Mercer, T. H. & Gleeson, N. P. Time-of-day dependence of isokinetic leg strength and associated interday variability. Br. J. Sports Med. 28, 167–170 (1994).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Gauthier, A., Davenne, D., Martin, A., Cometti, G. & Van Hoecke, J. Diurnal rhythm of the muscular performance of elbow flexors during isometric contractions. Chronobiol. Int. 13, 135–146 (1996).

    Article  CAS  PubMed  Google Scholar 

  56. Gauthier, A., Davenne, D., Gentil, C. & Van Hoecke, J. Circadian rhythm in the torque developed by elbow flexors during isometric contraction. Effect of sampling schedules. Chronobiol. Int. 14, 287–294 (1997).

    Article  CAS  PubMed  Google Scholar 

  57. Martin, A., Carpentier, A., Guissard, N., van Hoecke, J. & Duchateau, J. Effect of time of day on force variation in a human muscle. Muscle Nerve 22, 1380–1387 (1999).

    Article  CAS  PubMed  Google Scholar 

  58. Callard, D., Davenne, D., Gauthier, A., Lagarde, D. & Van Hoecke, J. Circadian rhythms in human muscular efficiency: continuous physical exercise versus continuous rest. A crossover study. Chronobiol. Int. 17, 693–704 (2000).

    Article  CAS  PubMed  Google Scholar 

  59. Souissi, N., Gauthier, A., Sesboue, B., Larue, J. & Davenne, D. Effects of regular training at the same time of day on diurnal fluctuations in muscular performance. J. Sports Sci. 20, 929–937 (2002).

    Article  PubMed  Google Scholar 

  60. Souissi, N., Sesboue, B., Gauthier, A., Larue, J. & Davenne, D. Effects of one night’s sleep deprivation on anaerobic performance the following day. Eur. J. Appl. Physiol. 89, 359–366 (2003).

    Article  PubMed  Google Scholar 

  61. Castaingts, V., Martin, A., Van Hoecke, J. & Perot, C. Neuromuscular efficiency of the triceps surae in induced and voluntary contractions: morning and evening evaluations. Chronobiol. Int. 21, 631–643 (2004).

    Article  CAS  PubMed  Google Scholar 

  62. Chtourou, H. et al. The effect of strength training at the same time of the day on the diurnal fluctuations of muscular anaerobic performances. J. Strength Cond. Res. 26, 217–225 (2012).

    Article  PubMed  Google Scholar 

  63. Souissi, N. et al. Effect of time of day and partial sleep deprivation on short-term, high-power output. Chronobiol. Int. 25, 1062–1076 (2008).

    Article  PubMed  Google Scholar 

  64. Taylor, K., Cronin, J. B., Gill, N., Chapman, D. W. & Sheppard, J. M. Warm-up affects diurnal variation in power output. Int. J. Sports Med. 32, 185–189 (2011).

    Article  CAS  PubMed  Google Scholar 

  65. Sedliak, M. et al. Morphological, molecular and hormonal adaptations to early morning versus afternoon resistance training. Chronobiol. Int. 35, 450–464 (2018).

    Article  CAS  PubMed  Google Scholar 

  66. Bernard, T., Giacomoni, M., Gavarry, O., Seymat, M. & Falgairette, G. Time-of-day effects in maximal anaerobic leg exercise. Eur. J. Appl. Physiol. Occup. Physiol. 77, 133–138 (1998).

    Article  CAS  PubMed  Google Scholar 

  67. Racinais, S., Perrey, S., Denis, R. & Bishop, D. Maximal power, but not fatigability, is greater during repeated sprints performed in the afternoon. Chronobiol. Int. 27, 855–864 (2010).

    Article  PubMed  Google Scholar 

  68. Lericollais, R., Gauthier, A., Bessot, N., Sesboue, B. & Davenne, D. Time-of-day effects on fatigue during a sustained anaerobic test in well-trained cyclists. Chronobiol. Int. 26, 1622–1635 (2009).

    Article  PubMed  Google Scholar 

  69. Souissi, N. et al. Diurnal variation in Wingate test performances: influence of active warm-up. Chronobiol. Int. 27, 640–652 (2010).

    Article  PubMed  Google Scholar 

  70. Fernandes, A. L. et al. Effect of time of day on performance, hormonal and metabolic response during a 1000-M cycling time trial. PLOS ONE 9, e109954 (2014).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  71. Deschenes, M. R. et al. Chronobiological effects on exercise performance and selected physiological responses. Eur. J. Appl. Physiol. Occup. Physiol. 77, 249–256 (1998).

    Article  CAS  PubMed  Google Scholar 

  72. Waterhouse, J. et al. The circadian rhythm of core temperature: origin and some implications for exercise performance. Chronobiol. Int. 22, 207–225 (2005).

    Article  PubMed  Google Scholar 

  73. Boukelia, B., Fogarty, M. C., Davison, R. C. & Florida-James, G. D. Diurnal physiological and immunological responses to a 10-km run in highly trained athletes in an environmentally controlled condition of 6 degrees C. Eur. J. Appl. Physiol. 117, 1–6 (2017).

    Article  PubMed  Google Scholar 

  74. Dibner, C., Schibler, U. & Albrecht, U. The mammalian circadian timing system: organization and coordination of central and peripheral clocks. Annu. Rev. Physiol. 72, 517–549 (2010).

    Article  CAS  PubMed  Google Scholar 

  75. Edwards, B., Waterhouse, J., Reilly, T. & Atkinson, G. A comparison of the suitabilities of rectal, gut, and insulated axilla temperatures for measurement of the circadian rhythm of core temperature in field studies. Chronobiol. Int. 19, 579–597 (2002).

    Article  CAS  PubMed  Google Scholar 

  76. Gray, S. R., De Vito, G., Nimmo, M. A., Farina, D. & Ferguson, R. A. Skeletal muscle ATP turnover and muscle fiber conduction velocity are elevated at higher muscle temperatures during maximal power output development in humans. Am. J. Physiol. Regul. Integr. Comp. Physiol. 290, R376–R382 (2006).

    Article  CAS  PubMed  Google Scholar 

  77. Gray, S. R., Soderlund, K. & Ferguson, R. A. ATP and phosphocreatine utilization in single human muscle fibres during the development of maximal power output at elevated muscle temperatures. J. Sports Sci. 26, 701–707 (2008).

    Article  PubMed  Google Scholar 

  78. Gonzalez-Alonso, J. et al. Blood temperature and perfusion to exercising and non-exercising human limbs. Exp. Physiol. 100, 1118–1131 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  79. Bass, J. & Lazar, M. A. Circadian time signatures of fitness and disease. Science 354, 994–999 (2016).

    Article  CAS  PubMed  Google Scholar 

  80. Buhr, E. D., Yoo, S. H. & Takahashi, J. S. Temperature as a universal resetting cue for mammalian circadian oscillators. Science 330, 379–385 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Racinais, S., Cocking, S. & Periard, J. D. Sports and environmental temperature: from warming-up to heating-up. Temperature (Austin) 4, 227–257 (2017).

    Article  Google Scholar 

  82. Pullinger, S. A. et al. Diurnal variation in repeated sprint performance cannot be offset when rectal and muscle temperatures are at optimal levels (38.5 degrees C). Chronobiol. Int. 35, 1054–1065 (2018).

    Article  PubMed  Google Scholar 

  83. Deschenes, M. R. et al. Biorhythmic influences on functional capacity of human muscle and physiological responses. Med. Sci. Sports Exerc. 30, 1399–1407 (1998).

    CAS  PubMed  Google Scholar 

  84. Morton, R. W. et al. Neither load nor systemic hormones determine resistance training-mediated hypertrophy or strength gains in resistance-trained young men. J. Appl. Physiol. 121, 129–138 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  85. Atger, F., Mauvoisin, D., Weger, B., Gobet, C. & Gachon, F. Regulation of mammalian physiology by interconnected circadian and feeding rhythms. Front. Endocrinol. (Lausanne) 8, 42 (2017).

    Article  Google Scholar 

  86. Mattson, M. P. et al. Meal frequency and timing in health and disease. Proc. Natl Acad. Sci. USA 111, 16647–16653 (2014).

    Article  CAS  PubMed  Google Scholar 

  87. Milton, K. Hunter-gatherer diets-a different perspective. Am. J. Clin. Nutr. 71, 665–667 (2000).

    Article  CAS  PubMed  Google Scholar 

  88. Crittenden, A. N. & Schnorr, S. L. Current views on hunter-gatherer nutrition and the evolution of the human diet. Am. J. Phys. Anthropol. 162 (Suppl. 63), 84–109 (2017).

    Article  PubMed  Google Scholar 

  89. Lamia, K. A., Storch, K. F. & Weitz, C. J. Physiological significance of a peripheral tissue circadian clock. Proc. Natl Acad. Sci. USA 105, 15172–15177 (2008).

    Article  CAS  PubMed  Google Scholar 

  90. Harfmann, B. D. et al. Muscle-specific loss of Bmal1 leads to disrupted tissue glucose metabolism and systemic glucose homeostasis. Skelet. Muscle 6, 12 (2016).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  91. Moran-Ramos, S. et al. The suprachiasmatic nucleus drives day-night variations in postprandial triglyceride uptake into skeletal muscle and brown adipose tissue. Exp. Physiol. 102, 1584–1595 (2017).

    Article  CAS  PubMed  Google Scholar 

  92. Gabriel, B., Ratkevicius, A., Gray, P., Frenneaux, M. P. & Gray, S. R. High-intensity exercise attenuates postprandial lipaemia and markers of oxidative stress. Clin. Sci. 123, 313–321 (2012).

    Article  CAS  PubMed  Google Scholar 

  93. Gabriel, B. M. et al. The effect of high intensity interval exercise on postprandial triacylglycerol and leukocyte activation—monitored for 48h post exercise. PLOS ONE 8, e82669 (2013).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  94. Sato, S., Parr, E. B., Devlin, B. L., Hawley, J. A. & Sassone-Corsi, P. Human metabolomics reveal daily variations under nutritional challenges specific to serum and skeletal muscle. Mol. Metab. 16, 1–11 (2018).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  95. Jeukendrup, A. E. Periodized nutrition for athletes. Sports Med. 47, 51–63 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  96. Marquet, L. A. et al. Enhanced endurance performance by periodization of carbohydrate intake: “Sleep Low” strategy. Med. Sci. Sports Exerc. 48, 663–672 (2016).

    Article  CAS  PubMed  Google Scholar 

  97. Lane, S. C. et al. Effects of sleeping with reduced carbohydrate availability on acute training responses. J. Appl. Physiol. 119, 643–655 (2015).

    Article  CAS  PubMed  Google Scholar 

  98. Hawley, J. A., Lundby, C., Cotter, J. D. & Burke, L. M. Maximizing cellular adaptation to endurance exercise in skeletal muscle. Cell Metab. 27, 962–976 (2018).

    Article  CAS  PubMed  Google Scholar 

  99. Kuusmaa, M. et al. Effects of morning versus evening combined strength and endurance training on physical performance, muscle hypertrophy, and serum hormone concentrations. Appl. Physiol. Nutr. Metab. 41, 1285–1294 (2016).

    Article  CAS  PubMed  Google Scholar 

  100. Matsumoto, C. S. et al. PI3K-PTEN dysregulation leads to mTOR-driven upregulation of the core clock gene BMAL1 in normal and malignant epithelial cells. Oncotarget 7, 42393–42407 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  101. Ramanathan, C. et al. mTOR signaling regulates central and peripheral circadian clock function. PLOS Genet. 14, e1007369 (2018).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  102. Liu, D. et al. mTOR signaling in VIP neurons regulates circadian clock synchrony and olfaction. Proc. Natl Acad. Sci. USA 115, E3296–E3304 (2018).

    Article  CAS  PubMed  Google Scholar 

  103. Reeds, P. J., Palmer, R. M., Hay, S. M. & McMillan, D. N. Protein synthesis in skeletal muscle measured at different times during a 24 hour period. Biosci. Rep. 6, 209–213 (1986).

    Article  CAS  PubMed  Google Scholar 

  104. Chang, S. W., Yoshihara, T., Machida, S. & Naito, H. Circadian rhythm of intracellular protein synthesis signaling in rat cardiac and skeletal muscles. Biochem. Biophys. Rep. 9, 153–158 (2017).

    PubMed  Google Scholar 

  105. Gangwisch, J. E. et al. Sleep duration as a risk factor for diabetes incidence in a large US sample. Sleep 30, 1667–1673 (2007).

    Article  PubMed  PubMed Central  Google Scholar 

  106. Ogilvie, R. P. & Patel, S. R. The epidemiology of sleep and obesity. Sleep Health 3, 383–388 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  107. Zwighaft, Z. et al. Circadian clock control by polyamine levels through a mechanism that declines with age. Cell Metab. 22, 874–885 (2015).

    Article  CAS  PubMed  Google Scholar 

  108. Myllymaki, T. et al. Effects of vigorous late-night exercise on sleep quality and cardiac autonomic activity. J. Sleep Res. 20, 146–153 (2011).

    Article  PubMed  Google Scholar 

  109. Banno, M. et al. Exercise can improve sleep quality: a systematic review and meta-analysis. PeerJ 6, e5172 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  110. Youngstedt, S. D., O’Connor, P. J. & Dishman, R. K. The effects of acute exercise on sleep: a quantitative synthesis. Sleep 20, 203–214 (1997).

    Article  CAS  PubMed  Google Scholar 

  111. Murray, K. et al. The relations between sleep, time of physical activity, and time outdoors among adult women. PLOS ONE 12, e0182013 (2017).

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  112. Figueiro, M. G. et al. The impact of daytime light exposures on sleep and mood in office workers. Sleep Health 3, 204–215 (2017).

    Article  PubMed  Google Scholar 

  113. Harrington, J. M. Health effects of shift work and extended hours of work. Occup. Environ. Med. 58, 68–72 (2001).

    Article  PubMed Central  Google Scholar 

  114. Buxton, O. M. et al. Sleep restriction for 1 week reduces insulin sensitivity in healthy men. Diabetes 59, 2126–2133 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  115. Eastman, C. I., Hoese, E. K., Youngstedt, S. D. & Liu, L. Phase-shifting human circadian rhythms with exercise during the night shift. Physiol. Behav. 58, 1287–1291 (1995).

    Article  CAS  PubMed  Google Scholar 

  116. Youngstedt, S. D. et al. Circadian phase-shifting effects of bright light, exercise, and bright light + exercise. J. Circadian Rhythms 14, 2 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  117. Dempsey, P. C. et al. Interrupting prolonged sitting in type 2 diabetes: nocturnal persistence of improved glycaemic control. Diabetologia 60, 499–507 (2017).

    Article  CAS  PubMed  Google Scholar 

  118. Gabel, K. et al. Effects of 8-hour time restricted feeding on body weight and metabolic disease risk factors in obese adults: a pilot study. Nutr. Healthy. Aging 4, 345–353 (2018).

    Google Scholar 

  119. Friborg, O., Bjorvatn, B., Amponsah, B. & Pallesen, S. Associations between seasonal variations in day length (photoperiod), sleep timing, sleep quality and mood: a comparison between Ghana (5 degrees) and Norway (69 degrees). J. Sleep Res. 21, 176–184 (2012).

    Article  PubMed  Google Scholar 

  120. Renstrom, F. et al. Season-dependent associations of circadian rhythm-regulating loci (CRY1, CRY2 and MTNR1B) and glucose homeostasis: the GLACIER Study. Diabetologia 58, 997–1005 (2015).

    Article  PubMed  CAS  Google Scholar 

  121. Atkinson, G. & Drust, B. Seasonal rhythms and exercise. Clin. Sports Med. 24, e25–e34 (2005).

    Article  PubMed  Google Scholar 

  122. Honma, K., Honma, S., Kohsaka, M. & Fukuda, N. Seasonal variation in the human circadian rhythm: dissociation between sleep and temperature rhythm. Am. J. Physiol. 262, R885–R891 (1992).

    CAS  PubMed  Google Scholar 

  123. Chen, L. & Yang, G. PPARs integrate the mammalian clock and energy metabolism. PPAR Res. 2014, 653017 (2014).

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The authors are supported by grants from the Novo Nordisk Foundation (NNF14OC0011493, NNF14OC0009941 and NNF18CC0034900), the Wenner-Gren Foundation, the Swedish Research Council (2015–00165), the European Research Council (233285) and the Strategic Research Programme in Diabetes at Karolinska Institutet (2009–1068). The authors are grateful to B. Atkins for his contribution to figure design.

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B.M.G. and J.R.Z. contributed equally to all aspects of the article.

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Correspondence to Juleen R. Zierath.

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Glossary

Core clock

A set of protein-coding genes (active in nearly all mammalian cells) that oscillate in expression and activity in a circadian manner.

Training

Repeated bouts of exercise resulting in physiological adaptations.

Diurnal

A diurnal cycle is any pattern that recurs every 24 hours, not necessarily biological or intrinsic.

Zeitgeber

A rhythmically occurring natural phenomenon that acts as a cue in the regulation of the body’s circadian rhythms.

Oxygen consumption rate

The amount of oxygen consumed by metabolic processes in tissues, cells or organelles. When applied to measuring mitochondria, different metabolic states (states 1–5) of the mitochondria are used.

Chronotype

The interindividual differences in the circadian phase of activity patterns and sleep–wake cycles.

Maximal power output

Maximal intensity of exercise or skeletal muscle contraction measured by power output (Watts).

Maximal sprint

A short burst of intense exercise after which the individual is momentarily unable to continue owing to fatigue.

Cycle ergometer

A fixed cycling machine often used in fitness testing to estimate exercise intensity.

Periodized nutrition

The strategic combined use of exercise training and nutrition, or nutrition alone, with the overall aim to improve the physiological response to exercise training.

Voluntary muscle force

Skeletal muscle contraction force produced as a result of endogenous activation of motor neurons.

Acute exercise

A single exercise bout, rather than exercise training.

Sleep hygiene

Habits and practices that are conducive to sleeping well on a regular basis.

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Gabriel, B.M., Zierath, J.R. Circadian rhythms and exercise — re-setting the clock in metabolic disease. Nat Rev Endocrinol 15, 197–206 (2019). https://doi.org/10.1038/s41574-018-0150-x

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