Ayano Shiba , Paul de Goede , Roberta Tandari , Ewout Foppen , Nikita L. Korpel , Tom V. Coopmans , Tom P. Hellings , Merel W. Jansen , Annelou Ruitenberg , Wayne I.G.R. Ritsema , Chun-Xia Yi , Joram D. Mul , Dirk Jan Stenvers , Andries Kalsbeek
{"title":"雄性黑线大鼠肌肉时钟的改变需要限时喂食和限时跑步的协同作用","authors":"Ayano Shiba , Paul de Goede , Roberta Tandari , Ewout Foppen , Nikita L. Korpel , Tom V. Coopmans , Tom P. Hellings , Merel W. Jansen , Annelou Ruitenberg , Wayne I.G.R. Ritsema , Chun-Xia Yi , Joram D. Mul , Dirk Jan Stenvers , Andries Kalsbeek","doi":"10.1016/j.nbscr.2024.100106","DOIUrl":null,"url":null,"abstract":"<div><div>Circadian disruption is an important factor driving the current-day high prevalence of obesity and type-2 diabetes. While the impact of incorrect timing of caloric intake on circadian disruption is widely acknowlegded, the contribution of incorrect timing of physical activity remains relatively understudied. Here, we modeled the incorrect timing of physical activity in nightshift workers in male Wistar rats, by restricting running wheel access to the innate inactive (light) phase (LR). Controls included no wheel access (NR); access only during the innate active (dark) period (DR); or unrestricted (<em>ad libitum</em>) access (ALR). LR did not shift the phase of the muscle or liver clock, but dampened the muscle clock amplitude. As our previous study demonstrated that light-phase restricted feeding did shift the liver clock, but made the muscle clock arrhythmic, we next combined the time restriction of wheel and food access to either the light phase (LRLF) or dark phase (DRDF). LRLF produced a ∼12 h shift in the majority of clock gene rhythms in both skeletal muscle and liver. On the other hand, DRDF was most effective in reducing body weight and the accumulation of fat mass. Therefore, in order to shift the muscle clock in male Wistar rats, synergy between the timing of feeding and physical activity is necessary. These findings may contribute to further improve the design of lifestyle strategies that try to limit metabolic misalignment caused by circadian disruption.</div></div>","PeriodicalId":37827,"journal":{"name":"Neurobiology of Sleep and Circadian Rhythms","volume":"17 ","pages":"Article 100106"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S245199442400004X/pdfft?md5=55f77d77b927aa3fd8aec6e4581f4bd4&pid=1-s2.0-S245199442400004X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Synergy between time-restricted feeding and time-restricted running is necessary to shift the muscle clock in male wistar rats\",\"authors\":\"Ayano Shiba , Paul de Goede , Roberta Tandari , Ewout Foppen , Nikita L. Korpel , Tom V. Coopmans , Tom P. Hellings , Merel W. Jansen , Annelou Ruitenberg , Wayne I.G.R. Ritsema , Chun-Xia Yi , Joram D. Mul , Dirk Jan Stenvers , Andries Kalsbeek\",\"doi\":\"10.1016/j.nbscr.2024.100106\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Circadian disruption is an important factor driving the current-day high prevalence of obesity and type-2 diabetes. While the impact of incorrect timing of caloric intake on circadian disruption is widely acknowlegded, the contribution of incorrect timing of physical activity remains relatively understudied. Here, we modeled the incorrect timing of physical activity in nightshift workers in male Wistar rats, by restricting running wheel access to the innate inactive (light) phase (LR). Controls included no wheel access (NR); access only during the innate active (dark) period (DR); or unrestricted (<em>ad libitum</em>) access (ALR). LR did not shift the phase of the muscle or liver clock, but dampened the muscle clock amplitude. As our previous study demonstrated that light-phase restricted feeding did shift the liver clock, but made the muscle clock arrhythmic, we next combined the time restriction of wheel and food access to either the light phase (LRLF) or dark phase (DRDF). LRLF produced a ∼12 h shift in the majority of clock gene rhythms in both skeletal muscle and liver. On the other hand, DRDF was most effective in reducing body weight and the accumulation of fat mass. Therefore, in order to shift the muscle clock in male Wistar rats, synergy between the timing of feeding and physical activity is necessary. 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Synergy between time-restricted feeding and time-restricted running is necessary to shift the muscle clock in male wistar rats
Circadian disruption is an important factor driving the current-day high prevalence of obesity and type-2 diabetes. While the impact of incorrect timing of caloric intake on circadian disruption is widely acknowlegded, the contribution of incorrect timing of physical activity remains relatively understudied. Here, we modeled the incorrect timing of physical activity in nightshift workers in male Wistar rats, by restricting running wheel access to the innate inactive (light) phase (LR). Controls included no wheel access (NR); access only during the innate active (dark) period (DR); or unrestricted (ad libitum) access (ALR). LR did not shift the phase of the muscle or liver clock, but dampened the muscle clock amplitude. As our previous study demonstrated that light-phase restricted feeding did shift the liver clock, but made the muscle clock arrhythmic, we next combined the time restriction of wheel and food access to either the light phase (LRLF) or dark phase (DRDF). LRLF produced a ∼12 h shift in the majority of clock gene rhythms in both skeletal muscle and liver. On the other hand, DRDF was most effective in reducing body weight and the accumulation of fat mass. Therefore, in order to shift the muscle clock in male Wistar rats, synergy between the timing of feeding and physical activity is necessary. These findings may contribute to further improve the design of lifestyle strategies that try to limit metabolic misalignment caused by circadian disruption.
期刊介绍:
Neurobiology of Sleep and Circadian Rhythms is a multidisciplinary journal for the publication of original research and review articles on basic and translational research into sleep and circadian rhythms. The journal focuses on topics covering the mechanisms of sleep/wake and circadian regulation from molecular to systems level, and on the functional consequences of sleep and circadian disruption. A key aim of the journal is the translation of basic research findings to understand and treat sleep and circadian disorders. Topics include, but are not limited to: Basic and translational research, Molecular mechanisms, Genetics and epigenetics, Inflammation and immunology, Memory and learning, Neurological and neurodegenerative diseases, Neuropsychopharmacology and neuroendocrinology, Behavioral sleep and circadian disorders, Shiftwork, Social jetlag.