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牡荆素通过抑制 D-半乳糖诱导的早衰小鼠和应激诱导的早衰中的 JAK2/STAT3 促进抗衰老作用。

Vitexin promotes the anti-senescence effect via inhibiting JAK2/STAT3 in D-Galactose-induced progeria mice and stress-induced premature senescence.

机构信息

Shaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China; Engineering Research Center of Brain Diseases Drug Development, Universities of Shaanxi Province, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China.

The First Affiliated Hospital of Xi'an Medical University, Xi'an, China.

出版信息

Eur J Pharmacol. 2024 Oct 5;980:176865. doi: 10.1016/j.ejphar.2024.176865. Epub 2024 Jul 30.

Abstract

Vitexin is a natural flavonoid glycoside compound extracted from the leaves and seeds of Vitex negundo. It is widely distributed in the leaves and stems of numerous plants and exhibites remarkable anti-tumor, anti-inflammatory, and anti-hypertensive properties. However, whether vitexin presents the anti-aging and senescence prevention effect has not been fully elucidated. The purpose of this study is to investigate the effect of vitexin on progeria mice and cellular senescence, as well as its underlying molecular mechanisms. To generate a premature aging/senescence model in vivo and in vitro, we used D-galactose (D-gal), hydrogen peroxide (HO), and adriamycin (ADR), respectively. Our findings demonstrated that vitexin potentially delays D-gal-induced progeria mice; similar effects were observed in stress-induced premature senescent fibroblasts in culture. Interestingly, this effect of vitexin is closely correlated with the reduction of the senescence-associated secretory phenotype (SASP) and the inhibition of the SASP-related JAK2/STAT3 pathway. Furthermore, we determined that vitexin meets the pharmacological parameters using the freely available ADMET web tool. Collectively, our findings demonstrate that vitexin possesses anti-senescence and anti-aging properties due to the inhibition of SASP and suppression of JAK2/STAT3 signaling pathway.

摘要

圣约翰草提取物是从荆芥属植物的叶子和种子中提取的一种天然黄酮类糖苷化合物。它广泛分布于许多植物的叶子和茎中,具有显著的抗肿瘤、抗炎和降压作用。然而,圣约翰草提取物是否具有抗衰老和预防衰老的作用尚未完全阐明。本研究旨在探讨圣约翰草提取物对早老症小鼠和细胞衰老的影响及其潜在的分子机制。为了在体内和体外生成早衰/衰老模型,我们分别使用了 D-半乳糖(D-gal)、过氧化氢(HO)和阿霉素(ADR)。我们的研究结果表明,圣约翰草提取物可能延缓 D-gal 诱导的早老症小鼠的衰老;在体外应激诱导的过早衰老成纤维细胞中也观察到了类似的效果。有趣的是,这种圣约翰草提取物的作用与衰老相关分泌表型(SASP)的减少和 SASP 相关 JAK2/STAT3 途径的抑制密切相关。此外,我们使用免费的 ADMET 网络工具确定了圣约翰草提取物符合药理学参数。综上所述,我们的研究结果表明,圣约翰草提取物具有抗衰老和抗衰老特性,这归因于其对 SASP 的抑制作用和对 JAK2/STAT3 信号通路的抑制作用。

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