Kui-Jie-Ling capsule inhibits ulcerative colitis by modulating inflammation and gut microbiota.

IF 3.7 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Kun Li, Lengqiu Guo, Jinghua Yu, Yun Yang, Lan Wei, Chunyan Min, Xinkang Xu, Fang Li, Jiangyun Liu, Guangquan Zhou, Jian Zhang
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Abstract

Background and aim: Kui-Jie-Ling capsule (Kui-Jie-Ling) is a hospital preparation for ulcerative colitis (UC) in China. This study aimed at evaluating the protective effects and mechanisms of Kui-Jie-Ling and Kui-Jie-Ling combined with adalimumab on UC induced by dextran sulfate sodium (DSS).

Methods: Network pharmacology was combined with an animal experiment to reveal the targets of Kui-Jie-Ling alleviating UC. The UC model was established by drinking 2.5% DSS solution for 7 days. On the second day, the mice in the Kui-Jie-Ling group were orally administered with Kui-Jie-Ling (1.5 and 3.0 g/kg) daily for seven consecutive days, and the mice in the combination group were orally administered with Kui-Jie-Ling (3.0 g/kg) once a day for seven consecutive days and received one subcutaneous injection of adalimumab. The disease activity index, the colon length, the spleen index, the cytokines, the colon, the short-chain fatty acid content, and the gut microbiota in the colon were analyzed. The role of gut microbiota against UC was verified by fecal microbiota transplantation experiments.

Results: The animal study's results were consistent with the network pharmacology analysis, which reflected that Kui-Jie-Ling alleviated UC via multi-pathway. Kui-Jie-Ling ameliorated UC by inhibiting the formation of neutrophil extracellular traps (NETs), regulating inflammatory factors through the lipopolysaccharide-toll-like receptor 4/nuclear factor kappa B and interleukin-23-Janus kinase 2/signal transducer and activator of transcription 3 signaling pathway, and restoring intestinal homeostasis.

Conclusion: These studies provided the experimental basis for the clinical administration of Kui-Jie-Ling and Kui-Jie-Ling combined with adalimumab against UC.

桔梗苓胶囊通过调节炎症和肠道微生物群抑制溃疡性结肠炎
背景和目的:鳖甲煎丸是中国治疗溃疡性结肠炎(UC)的医院制剂。本研究旨在评估鳖甲软胶囊和鳖甲软胶囊联合阿达木单抗对葡聚糖硫酸钠(DSS)诱导的 UC 的保护作用和机制:方法:将网络药理学与动物实验相结合,揭示鳖甲煎丸缓解UC的靶点。方法:将网络药理学与动物实验相结合,揭示了魁界灵缓解 UC 的靶点。第二天,鳖甲灵组小鼠每天口服鳖甲灵(1.5和3.0克/千克),连续7天;联合组小鼠每天口服鳖甲灵(3.0克/千克),连续7天,同时皮下注射阿达木单抗1次。研究分析了疾病活动指数、结肠长度、脾脏指数、细胞因子、结肠、短链脂肪酸含量以及结肠中的肠道微生物群。粪便微生物群移植实验验证了肠道微生物群对 UC 的作用:结果:动物实验结果与网络药理学分析结果一致。结果:动物实验结果与网络药理学分析结果一致,反映出鳖甲灵通过多途径缓解UC,包括抑制中性粒细胞胞外陷阱(NETs)的形成,通过脂多糖-类鹅卵石受体4/核因子卡巴B和白细胞介素-23-破伤风激酶2/信号转导和转录激活因子3信号通路调节炎症因子,恢复肠道稳态等:这些研究为临床应用桔梗苓和桔梗苓联合阿达木单抗治疗UC提供了实验依据。
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来源期刊
CiteScore
7.90
自引率
2.40%
发文量
326
审稿时长
2.3 months
期刊介绍: Journal of Gastroenterology and Hepatology is produced 12 times per year and publishes peer-reviewed original papers, reviews and editorials concerned with clinical practice and research in the fields of hepatology, gastroenterology and endoscopy. Papers cover the medical, radiological, pathological, biochemical, physiological and historical aspects of the subject areas. All submitted papers are reviewed by at least two referees expert in the field of the submitted paper.
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