Department of Evolution, Ecology, and Organismal Biology, University of California, Riverside, CA 92521, USA.
Neuroscience Graduate Program, University of California, Riverside, CA 92521, USA.
Physiol Behav. 2021 May 15;234:113389. doi: 10.1016/j.physbeh.2021.113389. Epub 2021 Mar 16.
Exercise behavior is under partial genetic control, but it is also affected by numerous environmental factors, potentially including early-life experiences whose effects persist into adulthood. We studied genetic and early-life environmental effects on wheel-running behavior in a mouse model that includes four replicate high runner (HR) lines selectively bred for increased voluntary wheel running as young adults and four non-selected control (C) lines. In a full factorial design, mice from each line were granted wheel access or not and administered either standard or Western diet (WD) from weaning (3 weeks old) to 6 weeks of age (sexual maturity). In addition to acute effects, after a washout period of 8 weeks (∼6 human years) in which all mice had standard diet and no wheel access, we found both beneficial and detrimental effects of these early-life exposures. During the first week of treatments, WD increased distance run by 29% in C mice and 48% in HR mice (significant Diet × Linetype interaction), but diet effects disappeared by the third week. Across the three weeks of juvenile treatment, WD significantly increased fat mass (with lean mass as a covariate). Tested as adults, early-life exercise increased wheel running of C mice but not HR mice in the first week. Early-life exercise also reduced adult anxiety-like behavior and increased adult fasted blood glucose levels, triceps surae mass, subdermal fat pad mass, and brain mass, but decreased heart ventricle mass. Using fat mass as a covariate, early-life exercise treatment increased adult leptin concentration. In contrast, early-life WD increased adult wheel running of HR mice but not C mice. Early-life WD also increased adult lean mass and adult preference for Western diet in all groups. Surprisingly, early-life treatment had no significant effect on adult body fat or maximal aerobic capacity (VOmax). No previous study has tested for combined or interactive effects of early-life WD and exercise. Our results demonstrate that both factors can have long-lasting effects on adult voluntary exercise and related phenotypes, and that these effects are modulated by genetic background. Overall, the long-lasting effects of early-life exercise were more pervasive than those of WD, suggesting critical opportunities for health intervention in childhood habits, as well as possible threats from modern challenges. These results may be relevant for understanding potential effects of activity reductions and dietary changes associated with the obesity epidemic and COVID-19 pandemic.
运动行为受部分遗传控制,但也受许多环境因素影响,潜在因素包括可能持续到成年的早期生活经历。我们在一个包含四个高跑(HR)系的小鼠模型中研究了遗传和早期环境对跑步行为的影响,这些系是为了增加年轻成长期的自愿跑步而选择培育的,还有四个非选择的对照(C)系。在完全析因设计中,来自每条线的小鼠被给予或不给予轮子进入的机会,并从断奶(3 周龄)到 6 周龄(性成熟)接受标准或西方饮食(WD)。除了急性影响外,在 8 周的洗脱期后(大约相当于 6 个人类年),所有小鼠都接受标准饮食且没有轮子进入,我们发现这些早期暴露有有益和有害的影响。在治疗的第一周,WD 使 C 组小鼠的跑步距离增加了 29%,使 HR 组小鼠的跑步距离增加了 48%(饮食×线类型的显著交互作用),但到第三周饮食的影响就消失了。在青少年治疗的三周内,WD 显著增加了脂肪量(以瘦体重为协变量)。作为成年人进行测试时,早期运动增加了 C 组小鼠但没有增加 HR 组小鼠的轮子跑步。早期运动还降低了成年焦虑样行为并增加了空腹血糖水平、比目鱼肌质量、皮下脂肪垫质量和脑质量,但减少了心室质量。使用脂肪量作为协变量,早期运动处理增加了成年瘦素浓度。相比之下,早期 WD 增加了 HR 组小鼠但没有增加 C 组小鼠的成年轮子跑步。早期 WD 还增加了所有组的成年瘦肉量和对西方饮食的偏好。令人惊讶的是,早期治疗对成年体脂肪或最大有氧能力(VOmax)没有显著影响。以前没有研究测试过早期 WD 和运动的综合或交互作用。我们的结果表明,这两个因素都可以对成年自愿运动和相关表型产生持久的影响,并且这些影响受遗传背景的调节。总的来说,早期运动的持久影响比 WD 的影响更为普遍,这表明在儿童时期的习惯中进行健康干预以及从现代挑战中可能产生的威胁都具有关键机会。这些结果可能与理解与肥胖症流行和 COVID-19 大流行相关的活动减少和饮食变化的潜在影响有关。