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祛瘀护膜剂调控NLRP3/Caspase-1信号通路对RE模型大鼠食管黏膜修复的影响

徐心怡 杨欣 梁国强 朱惠萍 黄雪 王爱民 孙宏文

徐心怡, 杨欣, 梁国强, 朱惠萍, 黄雪, 王爱民, 孙宏文. 祛瘀护膜剂调控NLRP3/Caspase-1信号通路对RE模型大鼠食管黏膜修复的影响[J]. 南京中医药大学学报, 2022, 38(4): 315-322. doi: 10.14148/j.issn.1672-0482.2022.0315
引用本文: 徐心怡, 杨欣, 梁国强, 朱惠萍, 黄雪, 王爱民, 孙宏文. 祛瘀护膜剂调控NLRP3/Caspase-1信号通路对RE模型大鼠食管黏膜修复的影响[J]. 南京中医药大学学报, 2022, 38(4): 315-322. doi: 10.14148/j.issn.1672-0482.2022.0315
XU Xin-yi, YANG Xin, LIANG Guo-qiang, ZHU Hui-ping, HUANG Xue, WANG Ai-min, SUN Hong-wen. Effect of Quyu Humo Paste on the Repair of Esophageal Mucosa in Rats with Reflux Esophagitis by Regulating NLRP3/Caspase-1 Signaling Pathway[J]. Journal of Nanjing University of traditional Chinese Medicine, 2022, 38(4): 315-322. doi: 10.14148/j.issn.1672-0482.2022.0315
Citation: XU Xin-yi, YANG Xin, LIANG Guo-qiang, ZHU Hui-ping, HUANG Xue, WANG Ai-min, SUN Hong-wen. Effect of Quyu Humo Paste on the Repair of Esophageal Mucosa in Rats with Reflux Esophagitis by Regulating NLRP3/Caspase-1 Signaling Pathway[J]. Journal of Nanjing University of traditional Chinese Medicine, 2022, 38(4): 315-322. doi: 10.14148/j.issn.1672-0482.2022.0315

祛瘀护膜剂调控NLRP3/Caspase-1信号通路对RE模型大鼠食管黏膜修复的影响

doi: 10.14148/j.issn.1672-0482.2022.0315
基金项目: 

苏州市科技发展计划(民生科技)关键技术项目 SS202082

苏州市卫健委重点病种诊疗技术项目 LCZX201817

详细信息
    作者简介:

    徐心怡, 女, 硕士研究生, E-mail: 1304620907@qq.com

    通讯作者:

    孙宏文, 女, 主任中医师, 博士生导师, 主要从事中医内科学脾胃病临床研究, E-mail: shw8101@163.com

  • 中图分类号: R285.5

Effect of Quyu Humo Paste on the Repair of Esophageal Mucosa in Rats with Reflux Esophagitis by Regulating NLRP3/Caspase-1 Signaling Pathway

  • 摘要:   目的  从食管黏膜屏障修复的角度, 探讨祛瘀护膜剂对反流性食管炎(RE)模型大鼠核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)/天冬氨酸特异性半胱氨酸蛋白酶-1(Caspase-1)信号通路的影响, 揭示祛瘀护膜剂治疗RE的作用机制。  方法  将大鼠随机分空白组, 模型组, 西药组, 祛瘀护膜剂低、中、高剂量组, 每组10只。除空白组外, 其余5组均使用“4.2 mm幽门夹+2/3胃底结扎术”方法建立RE大鼠模型, 空白组及模型组予淀粉+蒸馏水, 祛瘀护膜剂低、中、高剂量组分别予祛瘀护膜剂0.54、1.62、4.86 g·kg-1, 西药组予铝镁加混悬液, 灌胃给药14 d。第15天采血后处死大鼠并取出食管组织。ELISA法检测大鼠血清Caspase-1、白细胞介素-1β(IL-1β)、白细胞介素-18(IL-18)水平, Western blot法检测食管组织中NLRP3、Caspase-1蛋白表达情况, HE染色光镜下观察食管组织病理变化。  结果  与空白组比较, 模型组血清Caspase-1、IL-1β、IL-18水平及食管组织中NLRP3、Caspase-1蛋白表达量显著升高(P < 0.001)。与模型组比较, 西药组及祛瘀护膜剂中、高剂量组血清Caspase-1、IL-1β、IL-18水平及食管组织中NLRP3、Caspase-1蛋白表达量显著下降(P < 0.001)。与西药组比较, 祛瘀护膜剂高剂量组食管组织中NLRP3、Caspase-1蛋白表达量明显下降(P < 0.01), 血清Caspase-1水平显著下降(P < 0.001)。  结论  祛瘀护膜剂通过抑制NLRP3信号通路的过度激活, 下调Caspase-1的表达, 降低IL-1β、IL-18水平, 拮抗食管炎症反应, 从而改善食管上皮损伤进而修复食管黏膜, 促进大鼠RE的愈合。

     

  • 图  1  各组大鼠体质量变化比较

    注: 与d1比较, $$P < 0.01;与空白组比较, ##P < 0.01; 与模型组比较, *P < 0.05, * *P < 0.01。x±s, n=9~10。

    Figure  1.  Comparison of body mass changes in each group

    图  2  各组大鼠病理组织学切片(HE, ×100)

    Figure  2.  Comparison of histopathological sections in each group (HE, ×100)

    图  3  各组大鼠光镜下食管黏膜病理组织学评分比较

    注: 与空白组比较, * * *P < 0.001;与模型组比较, #P < 0.05, ##P < 0.01, ###P < 0.001。x±s, n=9~10。

    Figure  3.  Comparison of esophageal mucosal pathological histological scores under photocopy in each group

    图  4  各组大鼠血清Caspase-1、IL-1β、IL-18水平比较

    注: 与空白组比较, * * *P < 0.001;与模型组比较, #P < 0.05, ###P < 0.001; 与西药组比较, $P < 0.05, $$P < 0.01, $$$P < 0.001;与祛瘀护膜剂低剂量组比较, △△P < 0.01, △△△P < 0.001;与祛瘀护膜剂中剂量组比较, ☆☆☆P < 0.001。x±s, n=9~10。

    Figure  4.  Comparison of serum Caspase-1, IL-1β and IL-18 levels in each group

    图  5  各组大鼠食管组织中NLRP3、Caspase-1蛋白表达比较

    注: 与空白组比较, * * *P < 0.001;与模型组比较, ###P < 0.001;与西药组比较, $$P < 0.01;与祛瘀护膜剂低剂量组比较, △△P < 0.01, △△△P < 0.001;与祛瘀护膜剂中剂量组比较, P < 0.05, ☆☆☆P < 0.001。x±s, n=9~10。

    Figure  5.  Comparison of protein expressions of NLRP3 and Caspase-1 in esophageal tissues in each group

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  • 收稿日期:  2021-05-30
  • 网络出版日期:  2022-04-13
  • 发布日期:  2022-04-10

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