Sleep deprivation stimulates adaptive thermogenesis by activating AMPK pathway in mice.

IF 1.7 3区 生物学 Q4 PHYSIOLOGY
Tian-Shu Zheng, Xin-Ran Gao, Rui-Ping Xu, Yi-Fei Zhao, Zhi-Teng Yang, De-Hua Wang
{"title":"Sleep deprivation stimulates adaptive thermogenesis by activating AMPK pathway in mice.","authors":"Tian-Shu Zheng, Xin-Ran Gao, Rui-Ping Xu, Yi-Fei Zhao, Zhi-Teng Yang, De-Hua Wang","doi":"10.1007/s00360-024-01590-0","DOIUrl":null,"url":null,"abstract":"<p><p>Sleep deprivation (SD) can affect the adaptive thermogenesis in laboratory rodents, but the molecular mechanism and the crosstalk with other organs remain largely unknown. In order to investigate the effects and mechanisms of SD on thermoregulation and energy metabolism, here we measured the changes of body weight, body fat mass, body temperature, resting metabolic rate (RMR), and thermogenic gene expression in brown adipose tissue (BAT), white adipose tissue (WAT), skeleton muscle and liver in C57BL/6J mice during 7-day SD with rotating rod sleep deprivation device. Results showed that compared with the control group, the body weight and body fat mass of SD mice were decreased and RMR of SD mice increased. The gene expression of Ampk, Pgc1α and Ucp1 which related to thermogenesis in BAT and WAT were significantly increased, and the expression of Ampk, Serca1, Serca2 and Ucp3 which related to thermogenesis in skeletal muscle were significantly increased in SD mice. Taken together, these data demonstrated that 7-day SD enhanced the adaptive thermogenesis in mice by activating AMPK, including the upregulation of the AMPK - PGC1α - UCP1 pathway in BAT, and the AMPK - UCP3 and SLN - SERCA pathway in skeleton muscle. Our data provide the molecular evidence for SD-stimulated adaptive thermogenesis and energy metabolism in small mammals.</p>","PeriodicalId":56033,"journal":{"name":"Journal of Comparative Physiology B-Biochemical Systems and Environmental Physiology","volume":" ","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2024-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Physiology B-Biochemical Systems and Environmental Physiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00360-024-01590-0","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHYSIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Sleep deprivation (SD) can affect the adaptive thermogenesis in laboratory rodents, but the molecular mechanism and the crosstalk with other organs remain largely unknown. In order to investigate the effects and mechanisms of SD on thermoregulation and energy metabolism, here we measured the changes of body weight, body fat mass, body temperature, resting metabolic rate (RMR), and thermogenic gene expression in brown adipose tissue (BAT), white adipose tissue (WAT), skeleton muscle and liver in C57BL/6J mice during 7-day SD with rotating rod sleep deprivation device. Results showed that compared with the control group, the body weight and body fat mass of SD mice were decreased and RMR of SD mice increased. The gene expression of Ampk, Pgc1α and Ucp1 which related to thermogenesis in BAT and WAT were significantly increased, and the expression of Ampk, Serca1, Serca2 and Ucp3 which related to thermogenesis in skeletal muscle were significantly increased in SD mice. Taken together, these data demonstrated that 7-day SD enhanced the adaptive thermogenesis in mice by activating AMPK, including the upregulation of the AMPK - PGC1α - UCP1 pathway in BAT, and the AMPK - UCP3 and SLN - SERCA pathway in skeleton muscle. Our data provide the molecular evidence for SD-stimulated adaptive thermogenesis and energy metabolism in small mammals.

剥夺睡眠通过激活 AMPK 途径刺激小鼠的适应性产热。
睡眠剥夺(SD)会影响实验室啮齿动物的适应性产热,但其分子机制以及与其他器官的相互关系仍不清楚。为了研究睡眠剥夺对体温调节和能量代谢的影响及其机制,我们利用旋转棒睡眠剥夺装置测定了C57BL/6J小鼠在7天睡眠剥夺期间体重、体脂量、体温、静息代谢率(RMR)以及棕色脂肪组织(BAT)、白色脂肪组织(WAT)、骨骼肌和肝脏产热基因表达的变化。结果表明,与对照组相比,SD小鼠的体重和体脂肪量下降,RMR增加。SD小鼠BAT和WAT中与产热相关的Ampk、Pgc1α和Ucp1基因表达明显增加,骨骼肌中与产热相关的Ampk、Serca1、Serca2和Ucp3基因表达明显增加。总之,这些数据表明,7 天 SD 可通过激活 AMPK 增强小鼠的适应性产热,包括上调 BAT 中的 AMPK - PGC1α - UCP1 通路,以及骨骼肌中的 AMPK - UCP3 和 SLN - SERCA 通路。我们的数据为SD刺激小型哺乳动物的适应性产热和能量代谢提供了分子证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.90
自引率
0.00%
发文量
51
审稿时长
3.5 months
期刊介绍: The Journal of Comparative Physiology B publishes peer-reviewed original articles and reviews on the comparative physiology of invertebrate and vertebrate animals. Special emphasis is placed on integrative studies that elucidate mechanisms at the whole-animal, organ, tissue, cellular and/or molecular levels. Review papers report on the current state of knowledge in an area of comparative physiology, and directions in which future research is needed.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信