Adiposity and comorbidities: favorable impact of caloric restriction.

Eric Ravussin, Leanne M Redman
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引用次数: 5

Abstract

The focus here is on research involving long-term calorie restriction (CR) to prevent or delay the incidence of the metabolic syndrome with age. The current societal environment is marked by overabundant accessibility of food coupled with a strong trend to reduced physical activity, both leading to the development of a constellation of disorders including central obesity, insulin resistance, dyslipidemia and hypertension (metabolic syndrome). Prolonged CR has been shown to extend median and maximal lifespan in a variety of lower species (yeast, worms, fish, rats, and mice). Mechanisms of this lifespan extension by CR are not fully elucidated, but possibly involve alterations in energy metabolism, oxidative damage, insulin sensitivity, and functional changes in neuroendocrine systems. Ongoing studies of CR in humans now makes it possible to identify changes in 'biomarkers of aging' to unravel some of the mechanisms of its anti-aging phenomenon. Analyses from controlled human trials involving long-term CR will allow investigators to link observed alterations from body composition down to changes in molecular pathways and gene expression, with their possible effects on the metabolic syndrome and aging.

肥胖和合并症:热量限制的有利影响。
这里的重点是关于长期卡路里限制(CR)的研究,以防止或延缓代谢综合征随年龄的发生。当前社会环境的特点是食物供应过剩,同时体力活动明显减少,两者都导致了一系列疾病的发展,包括中枢性肥胖、胰岛素抵抗、血脂异常和高血压(代谢综合征)。延长CR已被证明可以延长多种低等物种(酵母、蠕虫、鱼、大鼠和小鼠)的中位和最大寿命。CR延长寿命的机制尚未完全阐明,但可能涉及能量代谢、氧化损伤、胰岛素敏感性和神经内分泌系统功能改变。目前,对人体CR的持续研究使得识别“衰老生物标志物”的变化成为可能,从而揭示其抗衰老现象的一些机制。包括长期CR的对照人体试验的分析将使研究人员能够将观察到的从身体组成到分子途径和基因表达的变化,以及它们对代谢综合征和衰老的可能影响联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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