Department of Pharmacology of Chinese Materia Medica, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.
FASEB J. 2019 Nov;33(11):12311-12323. doi: 10.1096/fj.201900425RR. Epub 2019 Aug 19.
The commensal microbiota is one of the environmental triggers of rheumatoid arthritis (RA). Recent studies have identified the characteristics of the gut microbiota in patients with RA. However, it is still unclear how the microbiota can be modulated to slow down disease progression. In the present study, berberine, a modulator of gut microbiota with substantial anti-RA effect, was chosen to explore the mechanisms by which the microbiota modulators ameliorate RA. The results showed that oral administration of berberine alleviated collagen-induced arthritis (CIA) in rats in a gut microbiota-dependent manner. Berberine down-regulated the diversity and richness of the gut bacteria, reduced the abundance of , and elevated the abundance of butyrate-producing bacteria in CIA rats as determined by the 16S rRNA gene sequence, which might function through limiting the generation of nitrate and stabilizing the physiologic hypoxia in the intestine. Moreover, berberine treatment significantly increased the intestinal butyrate level and promoted the expression and activity of butyryl-CoA:acetate-CoA transferase (BUT). The coadministration of a BUT inhibitor largely diminished the adjustment of intestinal environment and the antiarthritic effect of berberine. In conclusion, modulators of the gut microbiota might serve as therapeutic agents for RA by inducing the butyrate generation through promoting the expression and activity of BUT.-Yue, M., Tao, Y., Fang, Y., Lian, X., Zhang, Q., Xia, Y., Wei, Z., Dai, Y. The gut microbiota modulator berberine ameliorates collagen-induced arthritis in rats by facilitating the generation of butyrate and adjusting the intestinal hypoxia and nitrate supply.
共生微生物群是类风湿关节炎 (RA) 的环境触发因素之一。最近的研究已经确定了 RA 患者肠道微生物群的特征。然而,目前尚不清楚如何调节微生物群以减缓疾病进展。在本研究中,选择了具有显著抗 RA 作用的肠道微生物群调节剂小檗碱,以探讨微生物群调节剂改善 RA 的机制。结果表明,小檗碱通过肠道微生物群依赖的方式缓解了胶原诱导性关节炎 (CIA) 大鼠的疾病。小檗碱下调了 CIA 大鼠肠道细菌的多样性和丰富度,降低了的丰度,增加了丁酸产生菌的丰度,16S rRNA 基因序列表明,这可能通过限制硝酸盐的产生和稳定肠道的生理性缺氧来发挥作用。此外,小檗碱治疗显著增加了肠道丁酸水平,并促进了丁酰辅酶 A:乙酸辅酶 A 转移酶 (BUT) 的表达和活性。BUT 抑制剂的共同给药在很大程度上减少了肠道环境的调节和小檗碱的抗关节炎作用。总之,肠道微生物群调节剂可能通过促进 BUT 的表达和活性来诱导丁酸的产生,从而调节肠道缺氧和硝酸盐供应,从而成为 RA 的治疗药物。