Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA; William S. Middleton Memorial Veterans Hospital, Madison, WI, USA; Interdepartmental Graduate Program in Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Knoebel Institute for Healthy Aging, University of Denver, Denver, CO, USA; Department of Biological Sciences, University of Denver, Denver, CO, USA.
Cell Rep. 2024 Sep 24;43(9):114663. doi: 10.1016/j.celrep.2024.114663. Epub 2024 Aug 20.
Calorie restriction (CR) extends lifespan and healthspan in diverse species. Comparing ad libitum- and CR-fed mice is challenging due to their significantly different feeding patterns, with CR-fed mice consuming their daily meal in 2 h and then subjecting themselves to a prolonged daily fast. Here, we examine how ad libitum- and CR-fed mice respond to tests performed at various times and fasting durations and find that the effects of CR-insulin sensitivity, circulating metabolite levels, and mechanistic target of rapamycin 1 (mTORC1) activity-result from the specific temporal conditions chosen, with CR-induced improvements in insulin sensitivity observed only after a prolonged fast, and the observed differences in mTORC1 activity between ad libitum- and CR-fed mice dependent upon both fasting duration and the specific tissue examined. Our results demonstrate that much of our understanding of the effects of CR are related to when, relative to feeding, we choose to examine the mice.
热量限制(CR)可延长多种物种的寿命和健康寿命。由于 CR 喂养的小鼠的进食模式有很大的不同,它们每天在 2 小时内吃完一顿饭,然后进行长时间的日常禁食,因此比较自由进食和 CR 喂养的小鼠具有挑战性。在这里,我们研究了自由进食和 CR 喂养的小鼠如何对不同时间和禁食时间进行的测试做出反应,发现 CR 对胰岛素敏感性、循环代谢物水平和雷帕霉素靶蛋白复合体 1(mTORC1)活性的影响源自于所选择的特定时间条件,只有在长时间禁食后才能观察到 CR 诱导的胰岛素敏感性改善,而自由进食和 CR 喂养的小鼠之间观察到的 mTORC1 活性差异取决于禁食时间和具体检查的组织。我们的结果表明,我们对 CR 影响的理解很大程度上取决于我们选择检查小鼠的时间,相对于进食时间。