Effects of three Chinese herbal therapies on gut microbiota and short-chain fatty acid metabolism in patients with mild, moderate, and severe ulcerative colitis: Multi-center, randomized, controlled trials

IF 4.7 2区 医学 Q2 IMMUNOLOGY International immunopharmacology Pub Date : 2025-03-14 DOI:10.1016/j.intimp.2025.114444
Na Li , Xuekai Shang , Lei Shi , Yalan Li , Tangyou Mao , Qing Wang , Junxiang Li , Guiying Peng
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Abstract

Background

Traditional Chinese medicines, as a burgeoning field of medication, significantly alleviate ulcerative colitis (UC) by improving intestinal microbiota-metabolism. Our previous studies demonstrated the significant efficacy of Hudi Enteric-coated capsules (HDEC), Qingchang Wenzhong decoction (QCWZ), and Modified Wumei pill (MWMP) using a mouse model of colitis. However, the mechanism of these therapies through the modulation of microbiota-metabolism remains uncertain.

Objective

Three multicenter randomized controlled trials were designed to explore the effects of three therapies on the microbiota-metabolism of UC patients with different severity.

Methods

A total of 143 patients with different severities of UC were recruited from 10 hospitals. The clinical efficacy of HDEC for mild UC, QCWZ for moderate UC, and MWMP for severe UC (SUCs) was evaluated by colorectal Mayo scores and systemic inflammatory indicators. The 16S rRNA sequencing and metabolomics were used to analyze intestinal microbiota and metabolite profiles.

Results

Three therapies used alone or combined with mesalazine (MS) were comparable to MS alone in improving Mayo scores and hematic inflammatory parameters. Microbial diversities and architectures of SUCs showed the greatest response to MWMP+MS than other medications, as reflected by the enriched Ruminococcus and Anaerostipes together with the reduced Enterococcus, Streptococcus, and Streptococcus anginosus. Furthermore, MWMP+MS boosted the production of the microbiota-derived short-chain fatty acids (SCFAs) of SUCs. These differential microbes and metabolites further displayed significant statistical relationships with clinical parameters.

Conclusion

Herbal therapies, especially MWMP+MS, effectively improve microbiota composition and SCFA metabolism, which correlates with the improvements of serum inflammatory markers and endoscopic findings in patients.

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三种中药疗法对轻、中、重度溃疡性结肠炎患者肠道菌群和短链脂肪酸代谢的影响:多中心、随机、对照试验
中药作为新兴的药物治疗领域,通过改善肠道菌群代谢来显著缓解溃疡性结肠炎(UC)。我们前期在结肠炎小鼠模型上的研究证实了虎地肠溶胶囊(HDEC)、清肠温中汤(QCWZ)和乌梅丸(MWMP)的显著疗效。然而,这些疗法通过调节微生物群代谢的机制仍不确定。目的设计3项多中心随机对照试验,探讨3种治疗方法对不同严重程度UC患者微生物代谢的影响。方法收集我院10家医院不同程度UC患者143例。HDEC治疗轻度UC, QCWZ治疗中度UC, MWMP治疗重度UC (suc)的临床疗效通过结肠Mayo评分和全身炎症指标进行评估。使用16S rRNA测序和代谢组学分析肠道微生物群和代谢物谱。结果三种单独使用或联合使用美沙拉嗪(MS)的治疗方法在改善Mayo评分和血液炎症参数方面与单独使用MS相当。与其他药物相比,SUCs的微生物多样性和结构对MWMP+MS的反应最大,体现在Ruminococcus和anaerosties的富集以及Enterococcus、Streptococcus和anginosus的减少。此外,MWMP+MS促进了SUCs微生物源性短链脂肪酸(SCFAs)的产生。这些差异微生物和代谢物进一步显示出与临床参数的显著统计学关系。结论中药治疗,特别是MWMP+MS治疗可有效改善患者的微生物群组成和SCFA代谢,这与患者血清炎症标志物和内镜检查结果的改善有关。
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来源期刊
CiteScore
8.40
自引率
3.60%
发文量
935
审稿时长
53 days
期刊介绍: International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome. The subject material appropriate for submission includes: • Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders. • Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state. • Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses. • Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action. • Agents that activate genes or modify transcription and translation within the immune response. • Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active. • Production, function and regulation of cytokines and their receptors. • Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.
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