自噬
生物
代谢组
心肌保护
长寿
细胞生物学
白藜芦醇
转录因子
药理学
生物化学
代谢组学
生物信息学
遗传学
基因
细胞凋亡
缺血
心脏病学
医学
作者
Andreas Zimmermann,Katharina Kainz,Sebastian J. Hofer,Maria A. Bauer,Sabrina Schroeder,Jörn Dengjel,Federico Pietrocola,Oliver Kepp,Christoph Ruckenstuhl,Tobias Eisenberg,Stephan J. Sigrist,Frank Madeo,Didac Carmona‐Gutiérrez,Guido Kroemer
出处
期刊:Autophagy
[Taylor & Francis]
日期:2019-06-28
卷期号:15 (9): 1662-1664
被引量:8
标识
DOI:10.1080/15548627.2019.1632623
摘要
The age-induced deterioration of the organism results in detrimental and ultimately lethal pathologies. The process of aging itself involves a plethora of different mechanisms that should be subverted concurrently to delay and/or prevent age-related maladies. We have identified a natural compound, 4,4ʹ-dimethoxychalcone (DMC), which promotes longevity in yeast, worms and flies, and protects mice from heart injury and liver toxicity. Interestingly, both the DMC-mediated lifespan extension and the cardioprotection depend on macroautophagy/autophagy whereas hepatoprotection does not. DMC induces autophagy by inhibiting specific GATA transcription factors (TFs), independently of the TORC1 kinase pathway. The autophagy-independent beneficial effects of DMC might involve its antioxidative properties. DMC treatment results in a phylogenetically conserved, systemic impact on the metabolome, which is most prominently characterized by changes in cellular amino acid composition. Altogether, DMC exerts multiple, geroprotective effects by igniting distinct pathways, and thus represents a potential pharmacological agent that delays aging through multipronged effects.
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