基础医学与临床 ›› 2025, Vol. 45 ›› Issue (10): 1306-1312.doi: 10.16352/j.issn.1001-6325.2025.10.1306

• 研究论文 • 上一篇    下一篇

原儿茶酸减轻溃疡性结肠炎大鼠的结肠损伤

李尔萃1, 李伟之2, 韩宁1, 陈思1, 范慧娟1*   

  1. 1.空军军医大学第二附属医院 消化内科,陕西 西安 710032;
    2.西安交通大学第一附属医院 消化内科,陕西 西安 710061
  • 收稿日期:2024-11-12 修回日期:2024-12-31 出版日期:2025-10-05 发布日期:2025-09-22
  • 通讯作者: *578817134@qq.com
  • 基金资助:
    陕西省重点研发计划项目(2021SF-126)

Protocatechuic acid alleviates colon injury in ulcerative colitis rats

LI Ercui1, LI Weizhi2, HAN Ning1, CHEN Si1, FAN Huijuan1*   

  1. 1. Department of Gastroenterology, the Second Affiliated Hospital of Air Force Medical University, Xi'an 710032;
    2. Department of Gastroenterology, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710061, China
  • Received:2024-11-12 Revised:2024-12-31 Online:2025-10-05 Published:2025-09-22
  • Contact: *578817134@qq.com

摘要: 目的 探讨原儿茶酸(PCA)对溃疡性结肠炎(UC)大鼠Toll样受体4(TLR4)/核因子-κB(NF-κB)信号通路的影响。方法 建模后将大鼠分为:对照组、模型组[5%三硝基苯磺酸(TNBS)诱导]、低(L-PCA)、中(M-PCA)、高剂量原儿茶酸组(H-PCA)(分别灌胃2 mL剂量为20、40和80 mg/kg的PCA)和干预模型组(LPS,灌胃2 mL 80 mg/kg的PCA,同时腹腔注射0.8 mg/kg的LPS),每组12只大鼠,均连续给药14 d。治疗结束后对大鼠进行疾病活动指数(DAI)评分,苏木精-伊红(HE)染色和TUNEL染色观察结肠形态和细胞凋亡,Western blot检测结肠Occludin、闭锁小带蛋白-1(ZO-1)、claudin-1、肿瘤坏死因子-α(TNF-α)、白介素(IL)-1β和IL-10、TLR4和p-p65/p65的蛋白水平,免疫组化染色检测结肠TLR4蛋白表达水平。结果 与对照组相比,模型组大鼠结肠出现明显损伤,DAI评分和TUNEL阳性率升高(P<0.05),TNF-α、IL-1β、TLR4和p-p65蛋白相对表达量均升高(P<0.05),Occludin、ZO-1、claudin-1和IL-10蛋白相对表达量均降低(P<0.05)。与模型组相比,L-PCA、M-PCA和H-PCA组大鼠结肠损伤减轻,DAI评分和TUNEL阳性率降低(P<0.05),TNF-α、IL-1β、TLR4和p-p65蛋白相对表达量均降低(P<0.05),Occludin、ZO-1、claudin-1和IL-10蛋白相对表达量均升高(P<0.05)。与H-PCA组相比,LPS组大鼠结肠损伤加重,DAI评分和TUNEL阳性率升高(P<0.05),TNF-α、IL-1β、TLR4和p-p65蛋白相对表达量均升高(P<0.05),Occludin、ZO-1、claudin-1和IL-10蛋白相对表达量均降低(P<0.05)。结论 原儿茶酸可以减轻TNBS诱导的UC大鼠结肠损伤,改善肠道屏障功能,抑制结肠炎性反应,该作用可能与TLR4/NF-κB信号通路有关。

关键词: 原儿茶酸, 溃疡性结肠炎, Toll样受体4, 核因子-κB, 肠屏障功能

Abstract: Objective To investigate the effect of protocatechuic acid (PCA) on Toll-like receptor 4 (TLR4)/nuclear factor-kappa B (NF-κB) signal pathway in rats with ulcerative colitis (UC). Methods After modeling, rats were divided into control group, model group (5% trinitrobenzene sulfonic acid (TNBS) induction), low (L-PCA), middle (M-PCA), high (H-PCA) dose protocatechuic acid group (rats were given with PCA at doses of 20, 40 and 80 mg/kg respectively), and intervention model group (LPS, rats were given with PCA at doses of 80 mg/kg and 0.8 mg/kg LPS solution intraperitoneally), and 12 rats in each group were given the drug continuously for 14 days. After treatment, rats were evaluated by disease activity index (DAI), and the morphology and apoptosis of colon were observed by hematoxylin eosin (HE) staining and TUNEL staining. The protein levels of Occludin, Zona occludens 1 (ZO-1), claudin-1, Tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, IL-10, TLR4 and p-p65/p65 in colon were detected by Western blotting. The expression of TLR4 protein in colon was detected by immunohistochemical staining. Results Compared with control group, the colon of model group rat showed obvious injury, DAI score and positive rate of TUNEL were increased (P<0.05), the relative protein expression of TNF-α, IL-1β, TLR4 and p-p65 were increased (P<0.05), the relative protein expression of Occludin, ZO-1, claudin-1 and IL-10 were decreased (P<0.05). Compared with model group, colonic injury was alleviated in L-PCA, M-PCA and H-PCA groups, DAI score and positive rate of TUNEL were decreased (P<0.05), the relative protein expression of TNF-α, IL-1β, TLR4 and p-p65 were decreased (P<0.05), the relative protein expression of Occludin, ZO-1, claudin-1 and IL-10 were increased (P<0.05). Compared with H-PCA group, colon injury was aggravated in LPS group, DAI score and positive rate of TUNEL were increased (P<0.05), the relative protein expression of TNF-α, IL-1β, TLR4 and p-p65 was increased (P<0.05), the relative protein expression of Occludin, ZO-1, claudin-1 and IL-10 was decreased (P<0.05). Conclusions Protocatechuic acid can alleviate TNBS-induced colon injury in UC rats, improve intestinal barrier function, and inhibit colon inflammatory response, the mechanism of which is related to the activation of TLR4/NF-κB signaling pathway.

Key words: protocatechuic acid, ulcerative colitis, Toll-like receptor 4, NF-κB, intestinal barrier function

中图分类号: