生物
表观遗传学
内生
代谢调节
代谢途径
转录因子
变构调节
计算生物学
代谢网络
生物信息学
营养感应
代谢组学
酶
钥匙(锁)
神经科学
转录调控
系统生物学
心理干预
代谢组
信号转导
后生
辅因子
基因表达调控
细胞生物学
有机体
代谢适应
作者
Yizhou Jiang,Jing‐Dong Han
出处
期刊:Aging Cell
[Wiley]
日期:2026-01-12
卷期号:25 (2): e70371-e70371
摘要
Aging is a multifactorial process influenced by genetic, environmental, and metabolic factors. Dysregulated nutrient sensing and metabolic dysfunction are hallmarks of aging, and reduction of insulin/IGF-1 signaling or metabolic interventions such as caloric restriction extend lifespan across species. Endogenous metabolites reflect and mediate these metabolic cues, linking nutrient status to epigenetic and transcriptional programs by serving as cofactors for chromatin-modifying enzymes or as allosteric modulators of transcription factors. Some metabolites have emerged as key regulators of longevity, integrating into networks to concurrently influence multiple aging-related pathways. In this review, we summarize evidence supporting the lifespan-extending effects of key endogenous metabolites across diverse model organisms and discuss their mechanisms of action. These insights underscore the potential of targeting metabolic networks as a multifaceted strategy to delay aging. Finally, we consider the translational promise of metabolite-based interventions to extend healthspan while minimizing adverse effects, and we note remaining challenges such as optimal dosing, context-specific effects, and demonstrating efficacy in humans.
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