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二甲双胍可减缓雄性猴子的衰老时钟。

Metformin decelerates aging clock in male monkeys.

机构信息

Key Laboratory of Organ Regeneration and Reconstruction, State Key Laboratory of Membrane Biology, State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

China National Center for Bioinformation, Beijing, China; Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China; University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Cell. 2024 Oct 31;187(22):6358-6378.e29. doi: 10.1016/j.cell.2024.08.021. Epub 2024 Sep 12.

Abstract

In a rigorous 40-month study, we evaluated the geroprotective effects of metformin on adult male cynomolgus monkeys, addressing a gap in primate aging research. The study encompassed a comprehensive suite of physiological, imaging, histological, and molecular evaluations, substantiating metformin's influence on delaying age-related phenotypes at the organismal level. Specifically, we leveraged pan-tissue transcriptomics, DNA methylomics, plasma proteomics, and metabolomics to develop innovative monkey aging clocks and applied these to gauge metformin's effects on aging. The results highlighted a significant slowing of aging indicators, notably a roughly 6-year regression in brain aging. Metformin exerts a substantial neuroprotective effect, preserving brain structure and enhancing cognitive ability. The geroprotective effects on primate neurons were partially mediated by the activation of Nrf2, a transcription factor with anti-oxidative capabilities. Our research pioneers the systemic reduction of multi-dimensional biological age in primates through metformin, paving the way for advancing pharmaceutical strategies against human aging.

摘要

在一项严格的 40 个月的研究中,我们评估了二甲双胍对成年雄性食蟹猴的抗衰老作用,填补了灵长类动物衰老研究的空白。该研究涵盖了一系列全面的生理、成像、组织学和分子评估,证实了二甲双胍对延缓机体水平与年龄相关表型的影响。具体来说,我们利用全组织转录组学、DNA 甲基化组学、血浆蛋白质组学和代谢组学来开发创新的猴衰老时钟,并应用这些时钟来评估二甲双胍对衰老的影响。结果突出表明衰老指标显著减缓,特别是大脑衰老大约倒退了 6 年。二甲双胍发挥了显著的神经保护作用,保护了大脑结构并增强了认知能力。二甲双胍对灵长类神经元的抗衰老作用部分是通过激活 Nrf2 介导的,Nrf2 是一种具有抗氧化能力的转录因子。我们的研究开创了通过二甲双胍在灵长类动物中系统降低多维生物年龄的先河,为推进针对人类衰老的药物策略铺平了道路。

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