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茶多酚通过靶向Nrf2/HO-1/GPX4信号通路减轻辐射诱导的铁死亡和肠道损伤。

Tea Polyphenols Mitigate Radiation-Induced Ferroptosis and Intestinal Injury by Targeting the Nrf2/HO-1/GPX4 Signaling Pathway.

作者信息

Li Runtian, Li Lintao, Wu Haiyang, Gan Hui, Wu Zhuona, Gu Ruolan, Zhu Xiaoxia, Liu Shuchen, Meng Zhiyun, Dou Guifang

机构信息

Beijing Institute of Radiation Medicine, 27 Taiping Road, Beijing 100850, China.

School of Public Health, University of South China, Hengyang 421001, China.

出版信息

Antioxidants (Basel). 2025 May 11;14(5):580. doi: 10.3390/antiox14050580.

DOI:10.3390/antiox14050580
PMID:40427462
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12108355/
Abstract

Radiation-induced intestinal injury (RIII) is a significant concern for cancer patients receiving radiation therapy, as it can lead to complications such as radiation enteropathy. Presently, there are limited options for preventing or treating RIII. Tea polyphenols (TP), found in tea, provide various health benefits, but their antiradiation mechanisms are not fully understood. C57BL/6 mice pre-treated with TP for five days showed a significant improvement in survival rates after being exposed to 10 Gy of Co radiation. In the same way, abdominal exposure to 15 Gy of Co radiation effectively mitigated radiation-induced colon shortening, damage to intestinal tissues, oxidative stress, the release of inflammatory factors, and disruptions in intestinal microbial balance. In addition, TP treatment lowered the elevation of reactive oxygen species (ROS), iron imbalance, mitochondrial damage, and ferroptosis in IEC-6 cells post-irradiation. Utilizing network pharmacology, molecular docking, and affinity testing, we identified that TP has the capability to target the Nrf2/HO-1/GPX4 signaling pathway, while EGCG, a principal constituent of TP, interacts with HSP90 and mitigates radiation-induced ferroptosis. These findings suggest that TP may serve as a promising therapeutic agent to alleviate radiation-induced intestinal injury (RII).

摘要

辐射诱导的肠道损伤(RIII)是接受放射治疗的癌症患者面临的一个重大问题,因为它会导致诸如放射性肠炎等并发症。目前,预防或治疗RIII的选择有限。茶叶中含有的茶多酚(TP)具有多种健康益处,但其抗辐射机制尚未完全明确。用TP预处理5天的C57BL/6小鼠在接受10 Gy的钴辐射后存活率有显著提高。同样,腹部接受15 Gy的钴辐射能有效减轻辐射诱导的结肠缩短、肠道组织损伤、氧化应激、炎症因子释放以及肠道微生物平衡紊乱。此外,TP处理降低了照射后IEC-6细胞中活性氧(ROS)升高、铁失衡、线粒体损伤和铁死亡。利用网络药理学、分子对接和亲和力测试,我们确定TP能够靶向Nrf2/HO-1/GPX4信号通路,而TP的主要成分表没食子儿茶素没食子酸酯(EGCG)与热休克蛋白90(HSP90)相互作用并减轻辐射诱导的铁死亡。这些发现表明,TP可能是一种有前景的治疗剂,可减轻辐射诱导的肠道损伤(RII)。

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本文引用的文献

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