内分泌成纤维细胞生长因子对全身能量代谢的昼夜节律调控

IF 3.2 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Zhenning Yang, Helmut Zarbl, Grace L Guo
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引用次数: 0

摘要

昼夜节律钟是一种内源性生化计时系统,它使生物体的生理和行为与地球约 24 小时的昼夜节律周期相协调。中央昼夜节律钟通过环境线索同步,分级控制全身的外周时钟。昼夜节律系统调节各种代谢信号通路,以维持哺乳动物在不断变化的环境条件下的全身代谢平衡。内分泌成纤维细胞生长因子(FGFs),即 FGF15/19、FGF21 和 FGF23,在调节胆汁酸、脂类、葡萄糖、蛋白质和矿物质的全身代谢中发挥着重要作用。最近的证据表明,内分泌 FGFs 作为营养传感器,通过调节代谢酶和激素的表达,介导外周时钟与能量平衡之间的多因素相互作用。环境应激因素或基因消减诱发的昼夜节律紊乱与代谢功能障碍和昼夜节律紊乱的成纤维细胞生长因子信号通路有关,而昼夜节律紊乱是代谢性疾病的发病机理之一。限时喂养可加强代谢信号的昼夜模式,从而改善代谢健康,预防代谢疾病。时间疗法(chronotherapy)是指有策略地选择给药时间,以最大限度地发挥药物的益处并减少药物的毒副作用,它能为疾病治疗方案中生物节律与药物代谢和毒性之间的联系提供新的见解。在此,我们回顾了全身代谢中内分泌 FGF21 信号的昼夜节律调控,以及昼夜节律功能紊乱对代谢性疾病发病和发展的潜在影响。我们还讨论了 "昼夜营养 "和 "昼夜疗法 "的潜力,以便为开发内分泌 FGFs 的定时干预措施提供信息,从而优化人体的全身代谢。意义声明 昼夜节律计时系统支配着生物体的生理、代谢和行为功能。内分泌成纤维细胞生长因子(FGF)家族(FGF15/19、FGF21 和 FGF23)在调节能量和矿物质代谢方面发挥着重要作用。内分泌 FGF 起着营养传感器的作用,介导昼夜节律和新陈代谢平衡之间的多因素相互作用。长期扰乱昼夜节律会增加患代谢性疾病的风险。昼夜节律干预措施,如昼夜营养和昼夜疗法,为将生物节律与疾病预防和治疗联系起来提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circadian Regulation of Endocrine Fibroblast Growth Factors on Systemic Energy Metabolism.

The circadian clock is an endogenous biochemical timing system that coordinates the physiology and behavior of organisms to earth's ∼24-hour circadian day/night cycle. The central circadian clock synchronized by environmental cues hierarchically entrains peripheral clocks throughout the body. The circadian system modulates a wide variety of metabolic signaling pathways to maintain whole-body metabolic homeostasis in mammals under changing environmental conditions. Endocrine fibroblast growth factors (FGFs), namely FGF15/19, FGF21, and FGF23, play an important role in regulating systemic metabolism of bile acids, lipids, glucose, proteins, and minerals. Recent evidence indicates that endocrine FGFs function as nutrient sensors that mediate multifactorial interactions between peripheral clocks and energy homeostasis by regulating the expression of metabolic enzymes and hormones. Circadian disruption induced by environmental stressors or genetic ablation is associated with metabolic dysfunction and diurnal disturbances in FGF signaling pathways that contribute to the pathogenesis of metabolic diseases. Time-restricted feeding strengthens the circadian pattern of metabolic signals to improve metabolic health and prevent against metabolic diseases. Chronotherapy, the strategic timing of medication administration to maximize beneficial effects and minimize toxic effects, can provide novel insights into linking biologic rhythms to drug metabolism and toxicity within the therapeutical regimens of diseases. Here we review the circadian regulation of endocrine FGF signaling in whole-body metabolism and the potential effect of circadian dysfunction on the pathogenesis and development of metabolic diseases. We also discuss the potential of chrononutrition and chronotherapy for informing the development of timing interventions with endocrine FGFs to optimize whole-body metabolism in humans. SIGNIFICANCE STATEMENT: The circadian timing system governs physiological, metabolic, and behavioral functions in living organisms. The endocrine fibroblast growth factor (FGF) family (FGF15/19, FGF21, and FGF23) plays an important role in regulating energy and mineral metabolism. Endocrine FGFs function as nutrient sensors that mediate multifactorial interactions between circadian clocks and metabolic homeostasis. Chronic disruption of circadian rhythms increases the risk of metabolic diseases. Chronological interventions such as chrononutrition and chronotherapy provide insights into linking biological rhythms to disease prevention and treatment.

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来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
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