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Energy restriction and aging.

机译:能量限制和老化。

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摘要

PURPOSE OF REVIEW: The focus of this review is on current research involving long-term calorie restriction and the resulting changes observed in possible biomarkers of aging. Special emphasis will be given to the basic and clinical science studies which are currently investigating the effects of controlled, high-quality energy-restricted diets on both biomarkers of longevity and on the development of chronic diseases related to age and obesity in humans. RECENT FINDINGS: Prolonged calorie restriction has been shown to extend both the median and maximal lifespan in a variety of lower species such as yeast, worms, fish, rats, and mice. Mechanisms of this lifespan extension via calorie restriction are not fully elucidated, but possibly involve significant alterations in energy metabolism, oxidative damage, insulin sensitivity, and functional changes in both the neuroendocrine and sympathetic nervous systems. Ongoing studies of prolonged energy restriction in humans are now making it possible to analyze changes in these aging biomarkers to unravel some of the mechanisms of its antiaging phenomenon. SUMMARY: With the incremental expansion of research endeavors in the area of energy or calorie restriction, data on the effects of calorie restriction in animal models and humans are becoming more accessible. Detailed analyses from controlled human trials involving long-term calorie restriction will allow investigators to link observed alterations in body composition down to changes in molecular pathways and gene expression, with their possible effects on the biomarkers of aging.
机译:综述的目的:这篇综述的重点是当前的研究,该研究涉及长期卡路里限制以及在可能的衰老生物标志物中观察到的结果变化。将特别重视基础和临床科学研究,这些研究目前正在研究受控的高质量能量受限饮食对长寿生物标志物以及与人类年龄和肥胖有关的慢性疾病的发展的影响。最近的发现:延长卡路里的摄入量已显示出延长了各种低等物种(例如酵母,蠕虫,鱼类,大鼠和小鼠)的中位寿命和最大寿命。通过卡路里限制来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,胰岛素敏感性以及神经内分泌和交感神经系统功能改变的显着改变。正在进行的有关人类长期能量限制的研究现在使得分析这些衰老生物标志物的变化以阐明其抗衰老现象的某些机制成为可能。简介:随着能量或卡路里限制领域研究工作的不断扩展,关于卡路里限制在动物模型和人类中的作用的数据越来越容易获得。涉及长期卡路里限制的受控人体试验的详细分析将使研究人员可以将观察到的人体成分变化与分子途径和基因表达的变化联系起来,并可能对衰老的生物标志物产生影响。

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