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长寿之路上的一个关键转折点:寿命的分子基础愈发清晰。

A forkhead in the road to longevity: the molecular basis of lifespan becomes clearer.

作者信息

Morris Brian J

机构信息

Basic & Clinical Genomics Laboratory, School of Medical Sciences and Institute for Biomedical Research, Building F13, The University of Sydney, NSW 2006, Australia.

出版信息

J Hypertens. 2005 Jul;23(7):1285-309. doi: 10.1097/01.hjh.0000173509.45363.dd.

Abstract

OBJECTIVE

Although the quest for longevity is as old as civilization itself, only recently have technical and conceptual advances in genomics research brought us to the point of understanding the precise molecular events that make us age. This heralds an era when manipulations of these will enable us to live longer, healthier lives. The present review describes how recent experimental strategies have identified key genes and intracellular pathways that are responsible for ageing and longevity.

FINDINGS

In diverse species transcription factors belonging to the forkhead/winged helix box gene, group O (FOXO) subfamily have been found to be crucial in downstream suppression of the life-shortening effects of insulin/insulin-like growth factor-I receptor signalling pathways that, when upregulated, accelerate ageing by suppression of FOXO. The various adverse processes activated upon FOXO suppression include increased generation of reactive oxygen species (ROS). ROS are pivotal for the onset of various common conditions, including hypertension, atherosclerosis, type 2 diabetes, cancer and Alzheimer's disease, each of which shortens lifespan. In humans, FOXO3a, as well as FOXO1 and -4, and their downstream effectors, could hold the key to counteracting ageing and common diseases. An understanding of the processes controlled by these FOXOs should permit development of novel classes of agents that will more directly counteract or prevent the damage associated with diverse life-threatening conditions, and so foster a life of good health to a ripe old age. Just like caloric restriction, lifespan can be increased in various species by plant-derived polyphenols, such as resveratrol, via activation of sirtuins in cells. Sirtuins, such as SIRT1 in mammals, utilize FOXO and other pathways to achieve their beneficial effects on health and lifespan.

CONCLUSION

Lifespan is tractable and basic mechanisms are now known. Longevity research complements and overlaps research in most major medical disciplines. Current progress bodes well for an ever-increasing length of healthy life for those who adapt emerging knowledge personally (so-called 'longevitarians').

摘要

目的

尽管对长寿的追求与文明本身一样古老,但直到最近,基因组学研究在技术和概念上的进展才使我们能够理解导致我们衰老的精确分子事件。这预示着一个时代的到来,对这些事件的操控将使我们能够更长寿、更健康地生活。本综述描述了最近的实验策略如何确定了负责衰老和长寿的关键基因和细胞内途径。

研究结果

在多种物种中,属于叉头/翼状螺旋盒基因O组(FOXO)亚家族的转录因子已被发现对胰岛素/胰岛素样生长因子-I受体信号通路缩短寿命的作用具有关键的下游抑制作用,该信号通路上调时会通过抑制FOXO加速衰老。FOXO抑制后激活的各种不良过程包括活性氧(ROS)生成增加。ROS是各种常见病症发病的关键因素,包括高血压、动脉粥样硬化、2型糖尿病、癌症和阿尔茨海默病,每一种都会缩短寿命。在人类中,FOXO3a以及FOXO1和 -4及其下游效应器可能是对抗衰老和常见疾病的关键。了解这些FOXO所控制的过程应该能够开发出新型药物,这些药物将更直接地对抗或预防与各种危及生命的病症相关的损害,从而促进健康长寿。就像热量限制一样,植物来源的多酚(如白藜芦醇)可以通过激活细胞中的沉默调节蛋白来延长多种物种的寿命。沉默调节蛋白,如哺乳动物中的SIRT1,利用FOXO和其他途径对健康和寿命产生有益影响。

结论

寿命是可控的,基本机制现已明确。长寿研究与大多数主要医学学科的研究相互补充且有重叠。目前的进展对于那些亲身应用新知识的人(所谓的“长寿主义者”)来说,预示着健康寿命将不断延长。

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