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人参败毒散通过抑制PI3K/Akt/NF-κB信号通路保护溃疡性结肠炎。

Renshen Baidu powder protects ulcerative colitis inhibiting the PI3K/Akt/NF-κB signaling pathway.

作者信息

Ye Zhen, Li Yuzheng, She Yingqi, Wu Mingquan, Hu Yu, Qin Kaihua, Li Linzhen, Yu Han, Zhao Qian, Jin Zhao, Lu Fating, Ye Qiaobo

机构信息

School of Basic Medical Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Department of Pharmacy, Sichuan Orthopedic Hospital, Chengdu, China.

出版信息

Front Pharmacol. 2022 Aug 10;13:880589. doi: 10.3389/fphar.2022.880589. eCollection 2022.

Abstract

Ulcerative colitis is a chronic and relapsing inflammatory bowel disease without satisfactory therapy available recently. Renshen Baidu powder (RSBDP) is a classic Chinese medicinal formula used since Chinese Song dynasty and has been proven as an effective treatment of ulcerative colitis in clinics. However, the active ingredients and the molecular mechanism have not been fully disclosed. It is imperative to explore the active ingredients and the mechanism of RSBDP. In this study, the potential active components for ulcerative colitis treatment in RSBDP were determined and predicted in silicon, and its molecular mechanisms were also presented, in which the PI3K/Akt/NF-κB signaling pathway was recognized to be vital. Basically, the pharmacodynamics and mechanistic studies of RSBDP for ulcerative colitis were implemented on TNBS-induced experimental rats. The results showed that RSBDP could ameliorate the disease activity index and colon weight, as well as improve colonic shortening and colon histology. In addition, the tumor necrosis factor-α (TNF-α), diamine oxidase, intercellular adhesion molecule-1, and endotoxin in serum were also reduced. It is worth mentioning that the PI3K/Akt/NF-κB signaling pathway was inhibited after RSBDP administration inhibiting the phosphorylation of proteins. In conclusion, RSBDP effectively ameliorates TNBS-induced colitis rats by inhibiting the PI3K/Akt/NF-κB signaling pathway.

摘要

溃疡性结肠炎是一种慢性复发性炎症性肠病,目前尚无令人满意的治疗方法。人参败毒散(RSBDP)是自中国宋代以来使用的经典中药方剂,临床已证明其对溃疡性结肠炎有有效治疗作用。然而,其活性成分和分子机制尚未完全明确。探索RSBDP的活性成分和作用机制势在必行。本研究在计算机上确定并预测了RSBDP中治疗溃疡性结肠炎的潜在活性成分,并阐述了其分子机制,其中PI3K/Akt/NF-κB信号通路被认为至关重要。基本上,在三硝基苯磺酸(TNBS)诱导的实验大鼠上开展了RSBDP治疗溃疡性结肠炎的药效学和作用机制研究。结果表明,RSBDP可改善疾病活动指数和结肠重量,减轻结肠缩短并改善结肠组织学。此外,血清中的肿瘤坏死因子-α(TNF-α)、二胺氧化酶、细胞间黏附分子-1和内毒素也有所降低。值得一提的是,给予RSBDP后PI3K/Akt/NF-κB信号通路受到抑制,蛋白磷酸化受到抑制。总之,RSBDP通过抑制PI3K/Akt/NF-κB信号通路有效改善TNBS诱导的结肠炎大鼠症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70aa/9399752/b6a94aa63e66/fphar-13-880589-g001.jpg

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