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HDAC/NF-κB信号通路介导类风湿关节炎中的肠道微生物群失调:风湿宁汤的干预机制

HDAC/NF-κB signaling pathway mediates gut microbiota dysbiosis in rheumatoid arthritis: Intervention mechanisms of Fengshining decoction.

作者信息

Wen Ya, Li Mingyang, Hao Yuanhui, Peng Jiehao, Wei Xiuhong, Zhang Zhuanzhuan, Liu Biwang, Wang Yonghui, Peng Tao, Ma Yanmiao

机构信息

College of First Clinical Medicine, Shanxi University of Chinese Medicine, Taiyuan 030619, PR China.

College of Basic Medical Sciences, Shanxi University of Chinese Medicine, Taiyuan 030619, PR China.

出版信息

Phytomedicine. 2025 Sep;145:156976. doi: 10.1016/j.phymed.2025.156976. Epub 2025 Jun 16.

Abstract

BACKGROUND

Gut microbiota dysbiosis has been associated with the development of rheumatoid arthritis (RA). Fengshining (FSN) is a traditional Chinese medicine decoction that can effectively alleviate RA. However, how FSN modulates the gut microbiota to mitigate RA has not been comprehensively studied. This study evaluated the gut microecological mechanisms underlying FSN's effects on RA, focusing on the impact of gut-derived short-chain fatty acids (SCFAs), specifically butyrate, in RA treatment.

METHODS

The pharmacological effects of FSN on type II collagen-induced arthritis (CIA) in mice were assessed via pathological indicators, metagenomics, and metabolomics analyses. Furthermore, the impact of FSN on gut microbiota and metabolic profiles was also evaluated. Moreover, a pseudo-germ-free CIA model was established to validate whether exogenous butyrate alleviates RA. This study also elucidated whether fecal microbiota transplantation (FMT) from FSN-treated mice could mitigate RA symptoms.

RESULTS

The data showed that FSN markedly alleviated CIA symptoms and reduced serum inflammatory cytokine levels. Metagenomic and metabolomic analyses revealed that FSN-enriched SCFA-producing bacteria, including Butyrivibrio, Faecalicatena, and Lacrimispora. Furthermore, FSN increased the activity of carbohydrate metabolism-related enzymes and upregulated the expression patterns of homologous protein families. Moreover, exogenous butyrate supplementation suppressed pro-inflammatory factors, modulating immune responses, and enhanced intestinal barrier function. Further, Western blot analysis validated that FSN inhibited the HDAC/NF-κB pathway.

CONCLUSION

This study indicated that the gut microecological mechanism of FSN might be associated with its herbal components, which regulate gut microbiota diversity, restore the intestinal barrier, and boost microbial metabolite production. Furthermore, butyrate was observed to modulate intestinal mucosa, inhibit inflammatory responses, repair the intestinal barrier, and mitigate joint damage, thus alleviating RA symptoms.

摘要

背景

肠道微生物群失调与类风湿性关节炎(RA)的发展有关。风湿宁(FSN)是一种能有效缓解RA的中药汤剂。然而,FSN如何调节肠道微生物群以减轻RA尚未得到全面研究。本研究评估了FSN对RA作用的肠道微生态机制,重点关注肠道衍生的短链脂肪酸(SCFAs),特别是丁酸盐在RA治疗中的影响。

方法

通过病理指标、宏基因组学和代谢组学分析评估FSN对小鼠II型胶原诱导性关节炎(CIA)的药理作用。此外,还评估了FSN对肠道微生物群和代谢谱的影响。此外,建立了伪无菌CIA模型,以验证外源性丁酸盐是否能减轻RA。本研究还阐明了来自FSN处理小鼠的粪便微生物群移植(FMT)是否能减轻RA症状。

结果

数据显示,FSN显著减轻了CIA症状并降低了血清炎症细胞因子水平。宏基因组学和代谢组学分析表明,FSN富集了产生SCFA的细菌,包括丁酸弧菌属、粪链菌属和泪孢菌属。此外,FSN增加了碳水化合物代谢相关酶的活性,并上调了同源蛋白家族的表达模式。此外,补充外源性丁酸盐可抑制促炎因子,调节免疫反应,并增强肠道屏障功能。此外,蛋白质印迹分析证实FSN抑制了HDAC/NF-κB通路。

结论

本研究表明,FSN的肠道微生态机制可能与其草药成分有关,这些成分调节肠道微生物群多样性,恢复肠道屏障,并促进微生物代谢产物的产生。此外,观察到丁酸盐可调节肠黏膜,抑制炎症反应,修复肠道屏障,并减轻关节损伤,从而减轻RA症状。

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