Academy of Scientific & Innovative Research, Dietetics & Nutrition Technology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, India.
Academy of Scientific & Innovative Research, Dietetics & Nutrition Technology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, India.
J Nutr Biochem. 2022 Sep;107:109068. doi: 10.1016/j.jnutbio.2022.109068. Epub 2022 May 23.
Cellular senescence is emerging as a major hallmark of aging, and its modulation presents an effective anti-aging strategy. This study attempted to understand the progression of cellular senescence in vivo, and whether it can be mitigated by chronic consumption of green tea catechin epigallocatechin gallate (EGCG). We profiled cellular senescence in various organs of mice at four different time-points of lifespan, and then explored the influence of EGCG consumption in impacting markers of cellular senescence, inflamm-aging, immunosenescence, and gut dysbiosis. We report that visceral adipose and intestinal tissues are highly vulnerable to cellular senescence due to an increase in DNA damage response, activation of cell cycle inhibitors, and senescence-associated secretory phenotype regulators. With advancing age, dysregulation in nutrient signaling mediators (AMPK/AKT/SIRT3/5), and a decrease in autophagy was also observed. Inflamm-aging markers (TNF-α/IL-1β) and splenic CD4/CD8 T cell ratio increased with age, while NK cell population decreased. Metagenomic analyses revealed an age-related decrease in the diversity of microbial species and an increase in the abundance of various pathogenic bacterial species. On the other hand, long-term EGCG consumption significantly attenuated markers of DNA damage, cell cycle inhibitors, senescence-associated secretory phenotype regulators, AMPK/AKT signaling, and enhanced SIRT3/5 expression and autophagy. Systemic inflamm-aging indicators decreased, while early T cell activation increased in EGCG fed animals. EGCG also suppressed the abundance of pathogenic bacteria and preserved microbial diversity. Our results suggest that adipose and intestine tissues are prone to cellular senescence and that chronic consumption of EGCG can attenuate several deleterious aspects of aging which could be implicated in developing anti-aging strategies.
细胞衰老作为衰老的主要标志之一正在显现,其调控为抗衰老提供了一种有效策略。本研究试图了解体内细胞衰老的进展,以及慢性绿茶儿茶素表没食子儿茶素没食子酸酯(EGCG)的摄入是否可以减轻这种衰老。我们在小鼠的四个不同寿命时间点对其各种器官中的细胞衰老进行了分析,然后探讨了 EGCG 摄入对细胞衰老、炎症性衰老、免疫衰老和肠道菌群失调标志物的影响。我们报告称,由于 DNA 损伤反应增加、细胞周期抑制剂激活和衰老相关分泌表型调节剂增加,内脏脂肪和肠道组织极易发生细胞衰老。随着年龄的增长,还观察到营养信号转导介质(AMPK/AKT/SIRT3/5)失调和自噬减少。炎症性衰老标志物(TNF-α/IL-1β)和脾 CD4/CD8 T 细胞比值随年龄增加而增加,而 NK 细胞群体减少。宏基因组分析显示,随着年龄的增长,微生物物种的多样性减少,各种致病性细菌的丰度增加。另一方面,长期 EGCG 摄入可显著减弱 DNA 损伤、细胞周期抑制剂、衰老相关分泌表型调节剂、AMPK/AKT 信号转导的标志物,增强 SIRT3/5 的表达和自噬。全身性炎症性衰老标志物减少,而 EGCG 喂养动物的早期 T 细胞激活增加。EGCG 还抑制了病原菌的丰度并维持了微生物多样性。我们的结果表明,脂肪组织和肠道组织容易发生细胞衰老,慢性 EGCG 摄入可以减轻衰老的几个有害方面,这可能与开发抗衰老策略有关。