医学
药品
药物开发
老化
重症监护医学
机制(生物学)
药物发现
药理学
神经科学
临床实习
生物信息学
达沙替尼
计算生物学
药物靶点
转化研究
风险分析(工程)
临床试验
生物
疾病
药物重新定位
评论文章
作者
Ziying Zhou,Hongfei Duan,Si-Tu Xue,Zhuorong Li
标识
DOI:10.1016/j.arr.2025.102982
摘要
This review explores the anti-ageing potential of nine repurposed drugs: aspirin, atorvastatin, enalapril, metformin, canagliflozin, liraglutide, acarbose, N-acetylcysteine and dasatinib (commonly combined with quercetin). Specifically, it focuses on their mechanisms through the mechanistic target of rapamycin, adenosine monophosphate-activated protein kinase, nuclear factor kappa B and senescence-associated secretory phenotype pathways. The repurposed drugs show promise in extending healthspan and lifespan in model organisms by modulating ageing-related processes, e.g. reducing chronic inflammation, enhancing metabolic efficiency and improving cellular stress resistance. However, translating preclinical findings into clinical practice still faces major challenges, including species specificity and sex differences, the lack of reliable ageing biomarkers and the issue of dosage selection. This review synthesises progress and obstacles in transitioning drug development from targeting individual age-related diseases to addressing ageing as a unified biological process. Ultimately, the goal is to support a paradigm shift where ageing is recognised as a modifiable condition, enabling longer healthy human lifespans.
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