Li Min-Yao, Luo Hui-Juan, Wu Xue, Liu Yu-Hong, Gan Yu-Xuan, Xu Nan, Zhang Yao-Min, Zhang Shu-Hua, Zhou Chang-Lin, Su Zi-Ren, Huang Xiao-Qi, Zheng Xue-Bao
Mathematical Engineering Academy of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, China.
Dongguan Songshan Lake Yidao TCM Clinic, Dongguan, China.
Front Pharmacol. 2020 Jan 20;10:1552. doi: 10.3389/fphar.2019.01552. eCollection 2019.
Huangqin decoction (HQD), a classical traditional Chinese medicinal formula, has been commonly used to treat gastrointestinal diseases for thousands of years. We investigated the anti-inflammatory effects and underlying mechanisms of HQD on dextran sulfate sodium (DSS)-induced ulcerative colitis (UC).
Experimental mice were given 3% DSS, and HQD (2.275, 4.55, and 9.1 g/kg), or mesalazine (ME, 200 mg/kg) orally for 7 days. Body weight loss, disease activity index (DAI), colon length, histology, and levels of inflammatory cytokines were measured to evaluate the effects of HQD on colitis. The effects of HQD on the Ras-phosphoinositide-3-kinase (PI3K)-Akt-hypoxia inducible factor 1 alpha (HIF-1α) and nuclear factor-kappa B (NF-κB) pathways were evaluated by Western blot analysis. In addition, the gut microbiota was characterized using high-throughput Illumina MiSeq sequencing.
The results showed that HQD significantly reduced the body weight loss, ameliorated DAI, restored colon length, and improved the intestinal epithelial cell barrier in mice with DSS-induced colitis. The messenger RNA (mRNA) expression levels of inflammatory mediators were decreased following HQD treatment. Furthermore, the Ras-PI3K-Akt-HIF-1α and NF-κB pathways were significantly inhibited by HQD. Finally, treatment with HQD resulted in recovery of gut microbiota diversity.
HQD ameliorates DSS-induced colitis through regulation of the gut microbiota, and suppression of Ras-PI3K-Akt-HIF-1α and NF-κB pathways. Our results suggested that HQD may be a potential candidate for treatment of UC.
黄芩汤(HQD)是一种经典的中药方剂,数千年来一直常用于治疗胃肠道疾病。我们研究了HQD对葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎(UC)的抗炎作用及其潜在机制。
给实验小鼠口服3% DSS,并分别给予HQD(2.275、4.55和9.1 g/kg)或美沙拉嗪(ME,200 mg/kg),持续7天。测量体重减轻、疾病活动指数(DAI)、结肠长度、组织学以及炎症细胞因子水平,以评估HQD对结肠炎的影响。通过蛋白质免疫印迹分析评估HQD对Ras-磷酸肌醇-3-激酶(PI3K)-蛋白激酶B(Akt)-缺氧诱导因子1α(HIF-1α)和核因子-κB(NF-κB)信号通路的影响。此外,使用高通量Illumina MiSeq测序对肠道微生物群进行表征。
结果表明,HQD显著减轻了DSS诱导的结肠炎小鼠的体重减轻,改善了DAI,恢复了结肠长度,并改善了肠道上皮细胞屏障。HQD治疗后炎症介质的信使核糖核酸(mRNA)表达水平降低。此外,HQD显著抑制了Ras-PI3K-Akt-HIF-1α和NF-κB信号通路。最后,HQD治疗导致肠道微生物群多样性恢复。
HQD通过调节肠道微生物群以及抑制Ras-PI3K-Akt-HIF-1α和NF-κB信号通路来改善DSS诱导的结肠炎。我们的结果表明,HQD可能是治疗UC的潜在候选药物。