首页> 美国卫生研究院文献>PLoS Clinical Trials >Free Access to a Running-Wheel Advances the Phase of Behavioral and Physiological Circadian Rhythms and Peripheral Molecular Clocks in Mice
【2h】

Free Access to a Running-Wheel Advances the Phase of Behavioral and Physiological Circadian Rhythms and Peripheral Molecular Clocks in Mice

机译:免费进入跑步车轮可提高小鼠行为和生理昼夜节律及外围分子钟的相位

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Behavioral and physiological circadian rhythms are controlled by endogenous oscillators in animals. Voluntary wheel-running in rodents is thought to be an appropriate model of aerobic exercise in humans. We evaluated the effects of chronic voluntary exercise on the circadian system by analyzing temporal profiles of feeding, core body temperature, plasma hormone concentrations and peripheral expression of clock and clock-controlled genes in mice housed under sedentary (SED) conditions or given free access to a running-wheel (RW) for four weeks. Voluntary wheel-running activity advanced the circadian phases of increases in body temperature, food intake and corticosterone secretion in the mice. The circadian expression of clock and clock-controlled genes was tissue- and gene-specifically affected in the RW mice. The temporal expression of E-box-dependent circadian clock genes such as Per1, Per2, Nr1d1 and Dbp were slightly, but significantly phase-advanced in the liver and white adipose tissue, but not in brown adipose tissue and skeletal muscle. Peak levels of Per1, Per2 and Nr1d1 expression were significantly increased in the skeletal muscle of RW mice. The circadian phase and levels of hepatic mRNA expression of the clock-controlled genes that are involved in cholesterol and fatty acid metabolism significantly differed between SED and RW mice. These findings indicated that endogenous clock-governed voluntary wheel-running activity provides feedback to the central circadian clock that systemically governs behavioral and physiological rhythms.
机译:行为和生理昼夜节律受动物内源性振荡器控制。啮齿动物中的自愿轮转运动被认为是人类有氧运动的合适模型。我们通过分析在定居(SED)条件下或随意进食的小鼠的进食时间,核心体温,血浆激素浓度以及时钟和时钟控制基因的外周表达来评估慢性自愿运动对昼夜节律系统的影响。运行轮(RW)持续四个星期。自愿的车轮行驶活动使小鼠的体温,食物摄入和皮质酮分泌增加的昼夜节律阶段。在RW小鼠中,时钟和时钟控制基因的昼夜节律表达受到组织和基因特异性影响。 E-box依赖的昼夜节律基因,如Per1,Per2,Nr1d1和Dbp的时间表达在肝脏和白色脂肪组织中略微但明显地提前,而在棕色脂肪组织和骨骼肌中则没有。在RW小鼠的骨骼肌中,Per1,Per2和Nr1d1表达的峰值水平显着增加。在SED和RW小鼠之间,参与胆固醇和脂肪酸代谢的时钟控制基因的昼夜节律阶段和肝脏mRNA表达水平显着不同。这些发现表明,内源性时钟控制的自愿性轮转活动向中央昼夜节律时钟提供反馈,该昼夜节律时钟系统地控制行为和生理节律。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号