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肝脏作为日常代谢相互作用的枢纽。

Liver as a nexus of daily metabolic cross talk.

作者信息

Litwin Christopher, Koronowski Kevin B

机构信息

Department of Biochemistry & Structural Biology, University of Texas Health San Antonio, San Antonio, TX, United States; Sam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio, San Antonio, TX, United States.

Department of Biochemistry & Structural Biology, University of Texas Health San Antonio, San Antonio, TX, United States; Sam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio, San Antonio, TX, United States.

出版信息

Int Rev Cell Mol Biol. 2025;393:95-139. doi: 10.1016/bs.ircmb.2024.06.001. Epub 2024 Jun 25.

DOI:10.1016/bs.ircmb.2024.06.001
PMID:40390465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12092977/
Abstract

Over the course of a day, the circadian clock promotes a homeostatic balance between energy intake and energy expenditure by aligning metabolism with nutrient availability. In mammals, this process is driven by central clocks in the brain that control feeding behavior, the peripheral nervous system, and humoral outputs, as well as by peripheral clocks in non-brain tissues that regulate gene expression locally. Circadian organization of metabolism is critical, as circadian disruption is associated with increased risk of metabolic disease. Emerging evidence shows that circadian metabolism hinges upon inter-organ cross talk involving the liver, a metabolic hub that integrates many facets of systemic energy homeostasis. Here, we review spatiotemporal interactions, mainly metabolite exchange, signaling factors, and hormonal control, between the liver and skeletal muscle, pancreas, gut, microbiome, and adipose tissue. Modern society presents the challenge of circadian disturbances from rotating shift work to social jet lag and 24/7 food availability. Thus, it is important to better understand the mechanisms by which the clock system controls metabolic homeostasis and work toward targeted therapies.

摘要

在一天的过程中,生物钟通过使新陈代谢与营养物质的可利用性相匹配,促进能量摄入与能量消耗之间的稳态平衡。在哺乳动物中,这一过程由大脑中的中枢生物钟驱动,该中枢生物钟控制进食行为、外周神经系统和体液输出,以及由非脑组织中的外周生物钟局部调节基因表达。新陈代谢的昼夜节律组织至关重要,因为昼夜节律紊乱与代谢疾病风险增加有关。新出现的证据表明,昼夜节律代谢取决于涉及肝脏的器官间相互作用,肝脏是整合全身能量稳态多个方面的代谢枢纽。在这里,我们综述肝脏与骨骼肌、胰腺、肠道、微生物群和脂肪组织之间的时空相互作用,主要是代谢物交换、信号因子和激素控制。现代社会带来了昼夜节律紊乱的挑战,从轮班工作到社会时差以及全天候的食物供应。因此,更好地理解生物钟系统控制代谢稳态的机制并朝着靶向治疗努力很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/9600ba2991c0/nihms-2022011-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/4f5de939ea03/nihms-2022011-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/fb9346cb632d/nihms-2022011-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/fda2c69705af/nihms-2022011-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/9600ba2991c0/nihms-2022011-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/4f5de939ea03/nihms-2022011-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/fb9346cb632d/nihms-2022011-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/fda2c69705af/nihms-2022011-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/548d/12092977/9600ba2991c0/nihms-2022011-f0004.jpg

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本文引用的文献

1
Effect of Time-Restricted Eating on Weight Loss in Adults With Type 2 Diabetes: A Randomized Clinical Trial.限时进食对 2 型糖尿病成人减肥效果的随机临床试验。
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Impact of Bmal1 Rescue and Time-Restricted Feeding on Liver and Muscle Proteomes During the Active Phase in Mice.Bmal1 挽救和限时喂养对小鼠活动期肝脏和肌肉蛋白质组的影响。
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Meta-analysis of Diurnal Transcriptomics in Mouse Liver Reveals Low Repeatability of Rhythm Analyses.
基于小鼠肝脏的昼夜转录组学的荟萃分析显示节律分析的重复性低。
J Biol Rhythms. 2023 Dec;38(6):556-570. doi: 10.1177/07487304231179600. Epub 2023 Jun 29.
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Circadian regulation of liver function: from molecular mechanisms to disease pathophysiology.肝脏功能的昼夜节律调节:从分子机制到疾病病理生理学。
Nat Rev Gastroenterol Hepatol. 2023 Nov;20(11):695-707. doi: 10.1038/s41575-023-00792-1. Epub 2023 Jun 8.
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Liver and muscle circadian clocks cooperate to support glucose tolerance in mice.肝脏和肌肉生物钟协同作用,以维持小鼠的葡萄糖耐量。
Cell Rep. 2023 Jun 27;42(6):112588. doi: 10.1016/j.celrep.2023.112588. Epub 2023 Jun 1.
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Reprogramming of rhythmic liver metabolism by intestinal clock.肠道时钟对肝脏节律代谢的重编程。
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Mice with humanized livers reveal the role of hepatocyte clocks in rhythmic behavior.具有人类化肝脏的小鼠揭示了肝细胞时钟在节律行为中的作用。
Sci Adv. 2023 May 19;9(20):eadf2982. doi: 10.1126/sciadv.adf2982. Epub 2023 May 17.
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Organism-wide, cell-type-specific secretome mapping of exercise training in mice.整体生物体、细胞类型特异性的运动训练小鼠分泌组图谱。
Cell Metab. 2023 Jul 11;35(7):1261-1279.e11. doi: 10.1016/j.cmet.2023.04.011. Epub 2023 May 3.
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J Clin Invest. 2023 Apr 17;133(8):e163018. doi: 10.1172/JCI163018.
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