Therapeutic material basis and underling mechanisms of Shaoyao Decoction-exerted alleviation effects of colitis based on GPX4-regulated ferroptosis in epithelial cells

被引:36
作者
Li, Juan [1 ]
Tian, Xiangge [2 ]
Liu, Jinming [1 ]
Mo, Yuying [1 ]
Guo, Xiaoyi [1 ]
Qiu, Yang [1 ]
Liu, Yuejian [1 ]
Ma, Xiaochi [3 ]
Wang, Yan [4 ]
Xiong, Yongjian [1 ,4 ]
机构
[1] Dalian Med Univ, Cent Lab, Affiliated Hosp 1, Dalian 116011, Peoples R China
[2] Peking Univ Shenzhen Hosp, Dept Pharm, Shenzhen 518036, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 2, Pharmaceut Res Ctr, Dalian 116023, Peoples R China
[4] Dalian Med Univ, Coll Integrat Med, Dalian 116044, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
SYD; Ulcerative colitis; Epithelial barrier function; Ferroptosis in epithelial cells; GPX4; DELIVERY;
D O I
10.1186/s13020-022-00652-1
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Background Shaoyao Decoction (SYD) is a canonical herbal medicine prescription formulated by Liu Wan-Su in AD 1186. SYD has been widely used to treat inflammatory bowel disease by clearing heat and damp, removing stasis toxin in the intestine; however, the precise mechanisms and therapeutic material basis remain largely unclear. In the present study, we measured the effects of SYD on colitis symptom, epithelial barrier function, epithelial ferroptosis, colonic protein and mRNA expression of glutathione peroxidase 4 (GPX4) in colitis model, and determined whether SYD restored barrier loss in colitis by modulation of GPX4-regulated ferroptosis pathway. Methods Colitis was established by infusion with 1 mL 2,4,6-trinitrobenzene sulfonic acid (TNBS) dissolved in ethanol (40% v/v) in rats at a 125 mg/kg dose. Ferroptosis in epithelial cells was determined by flow cytometer. GPX4 promoter-firefly luciferase fusion construct was transfected to Caco-2 cell to determine GPX4 transcription. MS analysis was used to identified ingredients in SYD. Results Different doses of SYD significantly alleviated colitis, decreased ferroptosis in epithelial cells, knockout of GPX4 significantly reversed SYD-induced alleviation effects on colitis, restoration of epithelial barrier function, and epithelial ferroptosis. Wogonoside, wogonin, palmatine, paeoniflorin and liquiritin were identified as active ingredients of SYD-exerted alleviation effects of colitis based on GPX4 agonistic transcription. Conclusion SYD alleviated chemically induced colitis by activation of GPX4, inhibition of ferroptosis in epithelial cells and further restoration of barrier function. Wogonoside, wogonin, palmatine, paeoniflorin and liquiritin were identified as the key therapeutic material basis of SYD-exerted anti-colitis effects. The findings provide a scientific basis for the therapeutic effect of SYD on colitis.
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页数:13
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