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红茶水提取物通过激活抗氧化基因延长酵母寿命:抗衰老机制的转录组分析

Black Tea Aqueous Extract Extends Yeast Longevity via Antioxidant Gene Activation: Transcriptomic Analysis of Anti-Aging Mechanisms.

作者信息

Li Jie, Chen Qiyang, Xiao Fuliang, Yang Juan, Zhou Sijia, Tang Min, Hou Yujia, Zhai Xiuming

机构信息

Chongqing Academy of Agricultural Sciences Chongqing China.

Engineering Research Center of Biomass Materials, Ministry of Education, School of Life Sciences and Agri-Forestry Southwest University of Science and Technology Mianyang China.

出版信息

Food Sci Nutr. 2025 Jul 24;13(7):e70661. doi: 10.1002/fsn3.70661. eCollection 2025 Jul.

Abstract

Although tea polyphenols have antiaging potential, the molecular interplay between black tea components and cellular longevity remains unclear. This study has pioneered a dual approach combining lifespan assays with comprehensive transcriptomics to dissect how black tea aqueous extract (BTAE) extends the chronological lifespan (CLS). Remarkably, BTAE induced a dose-dependent lifespan extension (34.6% maximum at 40 μg/mL), coupled with a 62% reduction in reactive oxygen species (ROS) accumulation and enhanced superoxide dismutase/catalase/ascorbate peroxidase (SOD/CAT/APX) enzyme activities-hallmarks of antioxidant system activation. Transcriptomic profiling revealed the action mechanism of BTAE: (1) upregulation of oxidative defense arsenals (/, , and ) and mitochondrial efficiency genes (), and (2) strategic downregulation of apoptosis triggers ( and ) and aging accelerators ( and ). Additionally, we have identified novel targets including the -mediated membrane protection pathway and -dependent proteostatic regulation as key longevity switches. These findings establish BTAE as a multi-target anti-aging modulator and offer a roadmap for translating yeast discovery into mammalian aging interventions.

摘要

尽管茶多酚具有抗衰老潜力,但红茶成分与细胞寿命之间的分子相互作用仍不清楚。本研究开创了一种将寿命测定与综合转录组学相结合的双重方法,以剖析红茶水提取物(BTAE)如何延长时序寿命(CLS)。值得注意的是,BTAE诱导了剂量依赖性的寿命延长(40μg/mL时最大延长34.6%),同时活性氧(ROS)积累减少62%,超氧化物歧化酶/过氧化氢酶/抗坏血酸过氧化物酶(SOD/CAT/APX)酶活性增强——这是抗氧化系统激活的标志。转录组分析揭示了BTAE的作用机制:(1)上调氧化防御武器(/、和)和线粒体效率基因(),以及(2)战略性下调凋亡触发因子(和)和衰老加速因子(和)。此外,我们还确定了新的靶点,包括介导的膜保护途径和依赖的蛋白质稳态调节作为关键的长寿开关。这些发现确立了BTAE作为一种多靶点抗衰老调节剂,并为将酵母研究成果转化为哺乳动物衰老干预措施提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5023/12288370/07f3e32cc939/FSN3-13-e70661-g002.jpg

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