Dietary timing enhances exercise by modulating fat-muscle crosstalk via adipocyte AMPKa2 signaling
文献类型:期刊论文
| 作者 | Chen, Jianghui10,11; Xiang, Jing10,11; Zhou, Meiyu10,11; Huang, Rongfeng8,9,10,11; Zhang, Jianxin7,10,11; Cui, Yuanting10,11; Jiang, Xiaoqing10,11; Li, Yang10,11; Zhou, Runchao10,11; Xin, Haoran10,11 |
| 刊名 | CELL METABOLISM
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| 出版日期 | 2025-06-03 |
| 卷号 | 37期号:6页码:24 |
| ISSN号 | 1550-4131 |
| DOI | 10.1016/j.cmet.2025.02.007 |
| 英文摘要 | Feeding rhythms regulate exercise performance and muscle energy metabolism. However, the mechanisms regulating adipocyte functions remain unclear. Here, using multi-omics analyses, involving (phospho-)proteomics and lipidomics, we found that day-restricted feeding (DRF) regulates diurnal rhythms of the mitochondrial proteome, neutral lipidome, and nutrient-sensing pathways in mouse gonadal white adipose tissue (GWAT). Adipocyte-specific knockdown of Prkaa2 (the gene encoding AMPKa2) impairs physical endurance. This defect is associated with altered rhythmicity in acyl-coenzyme A (CoA) metabolism-related genes, a loss of rhythmicity in the GWAT lipidome, and circadian remodeling of serum metabolites-in particular, lactate and succinate. We also found that adipocyte Prkaa2 regulates muscle clock genes during DRF. Notably, oral administration of the AMPK activator C29 increases endurance and muscle functions in a time-of-day manner, which requires intact adipocyte AMPKa2 signaling. Collectively, our work defines adipocyte AMPKa2 signaling as a critical regulator of circadian metabolic coordination between fat and muscle, thereby enhancing exercise performance. |
| WOS关键词 | CIRCADIAN CLOCK ; INSULIN SENSITIVITY ; TIME ; METABOLISM ; PHOSPHORYLATION ; MICE ; ENDURANCE ; CAPACITY ; PLATFORM ; RHYTHMS |
| 资助项目 | National Natural Science Foundation of China[32471213] ; National Natural Science Foundation of China[92057109] ; National Natural Science Foundation of China[32400976] ; Noncommunicable Chronic Diseases-National Science and Technology Major Project[2023ZD0507800] ; Chongqing Science Fund for Distinguished Young Scholars[CSTB202 2NSCQ-JQX0009] ; Chongqing Municipal Health Commission[HBRC2 02405] ; Chongqing Technology Innovation and Application Demonstration Key Research and Development Project[CSTB2023TIAD-KPX0061-2] ; Chongqing Talent Program[CQYC20210303360] |
| WOS研究方向 | Cell Biology ; Endocrinology & Metabolism |
| 语种 | 英语 |
| WOS记录号 | WOS:001505238500005 |
| 出版者 | CELL PRESS |
| 源URL | [http://119.78.100.183/handle/2S10ELR8/318645] ![]() |
| 专题 | 新药研究国家重点实验室 |
| 通讯作者 | Zhang, Zhihui; Li, Min-Dian |
| 作者单位 | 1.PLA, Key Lab High Altitude Med, Chongqing 400038, Peoples R China 2.Minist Educ China, Key Lab Extreme Environm Med, Chongqing 400038, Peoples R China 3.Army Med Univ, Coll High Altitude Mil Med, Dept Pathophysiol, Chongqing 400038, Peoples R China 4.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China 5.LipidALL Technol Co Ltd, Changzhou, Peoples R China 6.Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Mol Dev Biol, Beijing 100101, Peoples R China 7.960th Hosp PLA Joint Serv Support Force, Dept Cardiol, Jinan 250000, Peoples R China 8.Sichuan Univ, West China Hosp 4, Chengdu 610072, Peoples R China 9.Sichuan Univ, West China Sch Publ Hlth, Dept Nutr & Food Hyg, Chengdu 610072, Peoples R China 10.Minist Educ Key Lab Geriatr Cardiovasc & Cerebrova, Key Lab Geriatr Cardiovasc & Cerebrovascular Dis, Chongqing 400038, Peoples R China |
| 推荐引用方式 GB/T 7714 | Chen, Jianghui,Xiang, Jing,Zhou, Meiyu,et al. Dietary timing enhances exercise by modulating fat-muscle crosstalk via adipocyte AMPKa2 signaling[J]. CELL METABOLISM,2025,37(6):24. |
| APA | Chen, Jianghui.,Xiang, Jing.,Zhou, Meiyu.,Huang, Rongfeng.,Zhang, Jianxin.,...&Li, Min-Dian.(2025).Dietary timing enhances exercise by modulating fat-muscle crosstalk via adipocyte AMPKa2 signaling.CELL METABOLISM,37(6),24. |
| MLA | Chen, Jianghui,et al."Dietary timing enhances exercise by modulating fat-muscle crosstalk via adipocyte AMPKa2 signaling".CELL METABOLISM 37.6(2025):24. |
入库方式: OAI收割
来源:上海药物研究所
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