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首页|期刊导航|中国药理学与毒理学杂志|胰岛素抵抗小鼠小肠类器官模型构建及黄诺玛苷对此模型肠黏膜屏障的保护作用

胰岛素抵抗小鼠小肠类器官模型构建及黄诺玛苷对此模型肠黏膜屏障的保护作用

依米妮古丽·麦麦提 李琳琳 麦麦提亚森·多力昆 古丽那孜·别克达吾来提 热孜亚·阿不来孜 陈龙 郑梦竹 杨占群 蔡梓恒 许诺

中国药理学与毒理学杂志2024,Vol.38Issue(2):105-112,8.
中国药理学与毒理学杂志2024,Vol.38Issue(2):105-112,8.DOI:10.3867/j.issn.1000-3002.2024.02.004

胰岛素抵抗小鼠小肠类器官模型构建及黄诺玛苷对此模型肠黏膜屏障的保护作用

Construction of small intestinal organoid model in insulin-resistant mice and protective effect of flavanomarein on intestinal mucosal barrier in this model

依米妮古丽·麦麦提 1李琳琳 1麦麦提亚森·多力昆 1古丽那孜·别克达吾来提 1热孜亚·阿不来孜 2陈龙 3郑梦竹 4杨占群 3蔡梓恒 1许诺1

作者信息

  • 1. 新疆医科大学药学院,新疆 乌鲁木齐 830011
  • 2. 新疆喀什地区第一人民医院综合心理科,新疆 喀什 844000
  • 3. 北京大学第三医院药剂科,北京 100191
  • 4. 北京大学第三医院药剂科,北京 100191||北京大学基因组学创新中心,北京 100091
  • 折叠

摘要

Abstract

OBJECTIVE To construct an insulin-resistant(IR)small intestinal organoid model of mice and study the protective effect of flavanomarein(FM)on the intestinal mucosal barrier in the model.METHODS ①Small intestinal organoid models of C57BL/6J and db/db of mice were constructed.The expressions of Ki-67,E-cadherin(E-cad),lysozyme(Lyz)and mucin-2(Muc-2)in small intestinal organ-oids were detected by 3D immunofluorescence.RT-qPCR was used to detect the expressions of fibro-nectin(Fn),glucagon-like peptide-1(GLP-1)and peotide YY(PYY)mRNA while Western blotting was used to detect the expressions of Fn,GLP-1 and PYY protein.The Lyz secretion level was detected by ELISA.② Small intestinal organoids were divided into five groups:C57BL/6J mice 'small intestinal organ-oids as the normal control group,db/db mice' intestinal organoids as the IR model group,db/db mice small intestinal organoids with flavanomarein 25,50 and 100 μmol·L-1 intervention for 48 h as IR model+ FM groups.RT-qPCR was used to detect the expression of Lyz mRNA while Western blotting was used to detect the expression of Lyz protein.RESULTS ① On the 6th day of small intestinal organoid culture,a ring structure with a clear luminal structure was formed and an IR mouse small intestinal organoid model was established.3D Immunofluorescence detection showed that the established small intestinal organoids all expressed Ki-67,E-cad,Lyz and MUC-2.Compared with the normal control group,the expres-sion of Fn mRNA in the IR model group was significantly increased(P<0.05)while the expressions of GLP-1 and PYY mRNA were significantly decreased(P<0.05).Compared with the normal control group,the expression of Fn protein in the IR model group was significantly decreased(P<0.05)while the expressions of GLP-1 and PYY protein were significantly increased(P<0.05).ELISA results showed that compared with the normal control group,the secretion levels of Lyz in the IR model group were signifi-cantly decreased(P<0.01).② RT-qPCR results showed that compared with the normal control group,the expression of Lyz mRNA in the IR model group was significantly decreased(P<0.01).Compared with the IR model group,the expression of Lyz mRNA in the IR model+FM 50 and 100 μmol·L-1 groups was significantly increased(P<0.05,P<0.01).Western blotting results showed that compared with the normal control group,the expression of Lyz protein in the IR model group was significantly decreased(P<0.01).Compared with the IR model group,the expression of Lyz protein in the IR model+FM 50 and 100 μmol·L-1 groups was significantly increased(P<0.05,P<0.01).CONCLUSION The constructed IR mouse small intestinal organoid model provides a more complete in vitro research model for exploring the pathophysiological mechanism by which drug interventions help repair the intestinal mucosal barrier.FM may maintain the intestinal mucosal barrier by reversing the decrease in Lyz expression levels in IR mice,thereby improving IR.

关键词

胰岛素抵抗/小肠类器官/黄诺玛苷/肠黏膜屏障/溶菌酶

Key words

insulin resistance/small intestinal organoids/flavanomarein/intestinal mucosal barrier/lysozymes

分类

医药卫生

引用本文复制引用

依米妮古丽·麦麦提,李琳琳,麦麦提亚森·多力昆,古丽那孜·别克达吾来提,热孜亚·阿不来孜,陈龙,郑梦竹,杨占群,蔡梓恒,许诺..胰岛素抵抗小鼠小肠类器官模型构建及黄诺玛苷对此模型肠黏膜屏障的保护作用[J].中国药理学与毒理学杂志,2024,38(2):105-112,8.

基金项目

新疆维吾尔自治区高等学校科研计划项目(XJE-DU2021I017) Xinjiang Uygur Autonomous Region Higher Education University Scientific Research Program(XJE-DU2021I017) (XJE-DU2021I017)

中国药理学与毒理学杂志

OA北大核心CSTPCD

1000-3002

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