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热量限制调节的分子途径及其对不同年龄组的影响:综述

Calorie Restriction-Regulated Molecular Pathways and Its Impact on Various Age Groups: An Overview.

作者信息

Rachakatla Anuradha, Kalashikam Rajender Rao

机构信息

Animal Facility, ICMR-National Institute of Nutrition, Hyderabad, India.

出版信息

DNA Cell Biol. 2022 May;41(5):459-468. doi: 10.1089/dna.2021.0922. Epub 2022 Apr 22.

DOI:10.1089/dna.2021.0922
PMID:35451872
Abstract

Calorie restriction (CR) if planned properly with regular exercise at different ages can result in healthy weight loss. CR can also have different beneficial effects on improving lifespan and decreasing the age-associated diseases by regulating physiological, biochemical, and molecular markers. The different pathways regulated by CR include:(1) AMP-activated protein kinase (AMPK), which involves PGC-1α, SIRT1, and SIRT3. AMPK also effects myocyte enhancer factor 2 (MEF2), peroxisome proliferator-activated receptor delta, and peroxisome proliferator-activated receptor alpha, which are involved in mitochondrial biogenesis and lipid oxidation; (2) Forkhead box transcription factor's signaling is related to the DNA repair, lipid metabolism, protection of protein structure, autophagy, and resistance to oxidative stress; (3) Mammalian target of rapamycin (mTOR) signaling, which involves key factors, such as S6 protein kinase-1 (S6K1), mTOR complex-1 (mTORC1), and 4E-binding protein (4E-BP). Under CR conditions, AMPK activation and mTOR inhibition helps in the activation of Ulk1 complex along with the acetyltransferase Mec-17, which is necessary for autophagy; (4) Insulin-like growth factor-1 (IGF-1) pathway downregulation protects against cancer and slows the aging process; (5) Nuclear factor kappa B pathway downregulation decreases the inflammation; and (6) c-Jun N-terminal kinase and p38 kinase regulation as a response to the stress. The acute and chronic CR both shows antidepression and anxiolytic action by effecting ghrelin/GHS-R1a signaling. CR also regulates GSK3β kinase and protects against age-related brain atrophy. CR at young age may show many deleterious effects by effecting different mechanisms. Parental CR before or during conception will also affect the health and development of the offspring by causing many epigenetic modifications that show transgenerational transmission. Maternal CR is associated with intrauterine growth retardation effecting the offspring in their adulthood by developing different metabolic syndromes. The epigenetic changes with response to paternal food supply also linked to offspring health. CR at middle and old age provides a significant preventive impact against the development of age-associated diseases.

摘要

如果在不同年龄段合理规划并结合规律运动,热量限制(CR)可实现健康减重。CR还可通过调节生理、生化和分子指标,对延长寿命及减少与年龄相关的疾病产生不同的有益影响。CR调节的不同途径包括:(1)AMP激活的蛋白激酶(AMPK),其涉及PGC-1α、SIRT1和SIRT3。AMPK还影响肌细胞增强因子2(MEF2)、过氧化物酶体增殖物激活受体δ和过氧化物酶体增殖物激活受体α,它们参与线粒体生物合成和脂质氧化;(2)叉头框转录因子信号传导与DNA修复、脂质代谢、蛋白质结构保护、自噬及抗氧化应激有关;(3)哺乳动物雷帕霉素靶蛋白(mTOR)信号传导,其涉及关键因子,如S6蛋白激酶-1(S6K1)、mTOR复合物-1(mTORC1)和4E结合蛋白(4E-BP)。在CR条件下,AMPK激活和mTOR抑制有助于激活Ulk1复合物以及乙酰转移酶Mec-17,这对自噬是必需的;(4)胰岛素样生长因子-1(IGF-1)途径下调可预防癌症并减缓衰老过程;(5)核因子κB途径下调可减轻炎症;(6)c-Jun氨基末端激酶和p38激酶调节作为对应激的反应。急性和慢性CR均通过影响胃饥饿素/GHS-R1a信号传导表现出抗抑郁和抗焦虑作用。CR还调节糖原合酶激酶3β(GSK3β)激酶并预防与年龄相关的脑萎缩。年轻时的CR可能通过影响不同机制产生许多有害影响。受孕前或受孕期间父母的CR也会通过引起许多显示跨代传递的表观遗传修饰,影响后代的健康和发育。母体CR与子宫内生长迟缓有关,会在成年后代中引发不同的代谢综合征,从而影响后代。对父本食物供应作出反应的表观遗传变化也与后代健康有关。中年和老年时的CR对预防与年龄相关疾病的发展具有显著作用。

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