Han Yuying, Liu Liya, Chen Youqin, Zheng Huifang, Yao Mengying, Cao Liujing, Sferra Thomas J, Ke Xiao, Peng Jun, Shen Aling
Clinical Research Institute, The Second Affiliated Hospital and Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Fujian Key Laboratory of Integrative Medicine in Geriatrics, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Front Pharmacol. 2023 Jul 27;14:1176579. doi: 10.3389/fphar.2023.1176579. eCollection 2023.
Qing Hua Chang Yin (QHCY) is a famous formula of traditional Chinese medicine (TCM) and has been proven to have protective effect on ulcerative colitis. However, its protective effect and potential therapeutic mechanisms in chronic colitis remain unclear. The purpose of this study is to explore the effects and underlying mechanisms of QHCY on dextran sulfate sodium (DSS)-induced chronic colitis mice model. The chronic colitis model was established by administration of 2% DSS for three consecutive cycles of 7 days with two intervals of 14 days for recovery by drinking water. The experiment lasted 49 days. The DSS + QHCY group received QHCY administration by oral gavage at doses of 1.6 g/kg/d, DSS + Mesalazine group was administrated Mesalazine by oral gavage at doses of 0.2 g/kg/d. The control and DSS group were given equal volume of distilled water. The body weight, stool consistency and blood in stool were monitored every 2 days. The disease activity index (DAI) was calculated. The colon length was measured after the mice were sacrificed. The histomorphology of colonic tissues was checked by the HE and PAS staining. Immunohistochemistry was performed to detect the expressions of pro-inflammatory cytokines (TNF-α, IL-1β and IL-6), tight junction proteins (ZO-1, occludin) and Mucin2 (MUC2). 16S rRNA sequencing analysis was conducted to study the diversity and abundance of gut microbiota changes. QHCY treatment not only significantly attenuated DSS-induced the weight loss, DAI score increase, colon shortening and histological damage in mice, but also decreased the expression of pro-inflammatory cytokines in colonic tissues and increased the expression of ZO-1, occludin, and MUC2. Furthermore, QHCY enhanced the diversity of gut microbes and regulated the structure and composition of intestinal microflora in mice with chronic colitis. QHCY has a therapeutic effect on a murine model of chronic colitis. It can effectively reduce the clinical and pathological manifestations of colitis and prevent alterations in the gut microbiota.
清化畅饮(QHCY)是一种著名的中药方剂,已被证明对溃疡性结肠炎具有保护作用。然而,其在慢性结肠炎中的保护作用及潜在治疗机制仍不清楚。本研究旨在探讨QHCY对葡聚糖硫酸钠(DSS)诱导的慢性结肠炎小鼠模型的影响及潜在机制。通过连续三个周期、为期7天的2% DSS饮水给药建立慢性结肠炎模型,中间间隔14天恢复,实验持续49天。DSS + QHCY组通过灌胃给予QHCY,剂量为1.6 g/kg/d,DSS + 美沙拉嗪组通过灌胃给予美沙拉嗪,剂量为0.2 g/kg/d。对照组和DSS组给予等量蒸馏水。每2天监测体重、粪便稠度和粪便潜血情况,计算疾病活动指数(DAI)。处死小鼠后测量结肠长度,通过苏木精-伊红(HE)和过碘酸雪夫(PAS)染色检查结肠组织的组织形态学。进行免疫组织化学检测促炎细胞因子(TNF-α、IL-1β和IL-6)、紧密连接蛋白(ZO-1、闭合蛋白)和黏蛋白2(MUC2)的表达。进行16S rRNA测序分析以研究肠道微生物群变化的多样性和丰度。QHCY治疗不仅显著减轻了DSS诱导的小鼠体重减轻、DAI评分增加、结肠缩短和组织学损伤,还降低了结肠组织中促炎细胞因子的表达,增加了ZO-1、闭合蛋白和MUC2的表达。此外,QHCY增强了肠道微生物的多样性,并调节了慢性结肠炎小鼠肠道微生物群的结构和组成。QHCY对慢性结肠炎小鼠模型具有治疗作用,可有效减轻结肠炎的临床和病理表现,并防止肠道微生物群的改变。