Department of Gastroenterology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China; School of Chinese Medicine, Hong Kong Baptist University, Hong Kong, China.
Department of Gastroenterology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Biomed Pharmacother. 2019 Oct;118:109206. doi: 10.1016/j.biopha.2019.109206. Epub 2019 Jul 12.
To investigate effects of berberine exerts on A20 expression and regulation of intestinal epithelial tight junctions via the TNF-α-NF-κB-MLCK pathway in Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D). C57BL/6 wild type (WT) and A20 IEC-KO mice (48 each) were randomly divided into normal control (NC), model control (MC), rifaximin and berberine groups (12 mice per group). An experimental model of IBS-D was established using 4% acetic acid and evaluated by haematoxylin-eosin (HE) staining. rifaximin and berberine mice were treated with rifaximin and berberine, respectively. Intestinal epithelial space of WT berberine mice improved more than A20 IEC-KO berberine mice compared to MC mice. WT berberine mice exhibited greater expression of A20 compared with MC mice(P < 0.01). TNF-α, NF-kB p65, MLCK, MLC, TRAF6 and RIP1 levels in A20 IEC-KO and WT berberine mice were all decreased compared to MC mice(P all<0.05). NF-κB p65, MLCK and TRAF6 levels were increased in A20 IEC-KO berberine mice as compared to WT berberine mice (P all<0.05). Intestinal epithelial levels of occludin, claudin-1, ZO-1 and F-actin increased in all berberine mice (P all<0.01-0.05), while occludin, claudin-1, and ZO-1 levels were lower in A20 IEC-KO berberine mice(P < 0.05). Berberine downregulates abnormal activation of the TNF-α-NF-κB-MLCK pathway by upregulating expression of A20 in a mouse model of IBS-D, thereby protecting intestinal epithelial tight junctions and repairing the damage IBS-D causes to the intestinal epithelial barrier.
研究小檗碱通过 TNF-α-NF-κB-MLCK 通路对 A20 表达的影响及其对腹泻型肠易激综合征(IBS-D)肠上皮紧密连接的调节作用。将 C57BL/6 野生型(WT)和 A20IEC-KO 小鼠(每组 48 只)随机分为正常对照组(NC)、模型对照组(MC)、利福昔明组和小檗碱组(每组 12 只)。采用 4%醋酸法建立 IBS-D 实验模型,采用苏木精-伊红(HE)染色进行评价。利福昔明和小檗碱组分别给予利福昔明和小檗碱处理。与 MC 组相比,WT 小檗碱组小鼠肠上皮细胞间隙改善更为明显,A20IEC-KO 小檗碱组则较 WT 小檗碱组改善更为明显。与 MC 组相比,WT 小檗碱组小鼠 A20 的表达增加更为明显(P<0.01)。与 MC 组相比,A20IEC-KO 和 WT 小檗碱组小鼠的 TNF-α、NF-κB p65、MLCK、MLC、TRAF6 和 RIP1 水平均降低(P<0.05)。与 WT 小檗碱组相比,A20IEC-KO 小檗碱组小鼠 NF-κB p65、MLCK 和 TRAF6 水平升高(P 均<0.05)。与 MC 组相比,所有小檗碱组小鼠的紧密连接蛋白 occludin、claudin-1、ZO-1 和 F-actin 水平均升高(P 均<0.01-0.05),而 A20IEC-KO 小檗碱组小鼠的 occludin、claudin-1 和 ZO-1 水平较低(P<0.05)。小檗碱通过上调 A20 的表达下调 IBS-D 小鼠 TNF-α-NF-κB-MLCK 通路的异常激活,从而保护肠上皮紧密连接,修复 IBS-D 对肠上皮屏障的损伤。