1. Resveratrol attenuates radiation enteritis through the SIRT1/FOXO3a and PI3K/AKT signaling pathways.
- Author
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Qin, Haoren, Zhang, Heng, Zhang, Xipeng, Zhang, Shiwu, Zhu, Siwei, and Wang, Hui
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RESVERATROL , *ENTERITIS , *RADIATION injuries , *LABORATORY mice , *INTESTINAL injuries , *SIRTUINS - Abstract
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. • Resveratrol pretreatment attenuated radiation-induced intestinal injury in mice. •Resveratrol mitigated irradiation-induced IEC-6 cell injury. •Resveratrol activated the SIRT1/FOXO3a pathway to inhibit oxidative stress. •The PI3K/AKT pathway may aid resveratrol protective effects against radiation. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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