Resveratrol attenuates radiation enteritis through the SIRT1/FOXO3a and PI3K/AKT signaling pathways

被引:35
|
作者
Qin, Haoren [1 ]
Zhang, Heng [2 ]
Zhang, Xipeng [3 ]
Zhang, Shiwu [4 ]
Zhu, Siwei [2 ]
Wang, Hui [2 ]
机构
[1] Tianjin Univ Tradit Chinese Med, Tianjin, Peoples R China
[2] Nankai Univ, Inst Integrat Oncol, Dept Oncol, Tianjin Union Med Ctr, 190 Jieyuan Rd, Tianjin 300121, Peoples R China
[3] Nankai Univ, Inst Translat Med, Dept Colorectal Surg, Tianjin Union Med Ctr, Tianjin, Peoples R China
[4] Nankai Univ, Inst Translat Med, Dept Pathol, Tianjin Union Med Ctr, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Radiation enteritis; Radioprotection; Resveratrol; Oxidative stress; SIRT1; FOXO3a signaling pathway; PI3K; AKT pathway;
D O I
10.1016/j.bbrc.2021.03.122
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Radiation enteritis (RE) is the most common radiotherapy complication, and effective RE treatments are lacking. Resveratrol exerts beneficial effects on radiation injury. However, the effect of resveratrol in radiation-induced intestinal injury and the underlying mechanism remain unclear. Here, a C57BL/6 mouse model of RE was established and an intestinal epithelial cell line was used to evaluate the protective effects of resveratrol against radiation-induced intestinal injury and the underlying mechanisms. Resveratrol improved radiation-induced oxidative stress and cell apoptosis via upregulating antioxidant enzymes and downregulating p53 acetylation. In vivo, resveratrol-treated mice exhibited longer survival; longer villi; more intestinal crypt cells; upregulated expression of Ki67, catalase, and superoxide dismutase 2; and fewer inflammatory proteins and apoptotic cells. These protective effects were suppressed by inhibition of SIRT1. These results demonstrate that resveratrol can reduce radiation-induced intestinal injury by inhibiting oxidative stress and apoptosis via the SIRT1/FOXO3a and PI3K/AKT pathways. ? 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
引用
收藏
页码:199 / 205
页数:7
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