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首页|期刊导航|海南医学院学报|大黄灵仙方调控肝内胆管细胞炎症大鼠的作用及机制研究

大黄灵仙方调控肝内胆管细胞炎症大鼠的作用及机制研究

庞浇安 李承积 俞渊 付军 叶桂源 陈伟棠 罗艳萍 滕金豪 刘春丽 肖丽君

海南医学院学报2024,Vol.30Issue(16):1201-1209,9.
海南医学院学报2024,Vol.30Issue(16):1201-1209,9.DOI:10.13210/j.cnki.jhmu.20240513.001

大黄灵仙方调控肝内胆管细胞炎症大鼠的作用及机制研究

Study on the effect and mechanism of Dahuang Lingxian formula on regulating intrahepatic bile duct cell inflammation in rats

庞浇安 1李承积 2俞渊 1付军 1叶桂源 1陈伟棠 1罗艳萍 1滕金豪 1刘春丽 3肖丽君4

作者信息

  • 1. 广西中医药大学第一附属医院,广西 南宁 530200
  • 2. 广西靖西市人民医院,广西 靖西 533000
  • 3. 中国人民解放军南部战区总医院,广东 广州 510000
  • 4. 桂林市中医医院,广西 桂林 541000
  • 折叠

摘要

Abstract

Objective:To observe the effects of Dahuang Lingxian formula on the expression levels of IKKα,ASK1,MKK3 and CX3CL1 key factors in the MAPK/NF-κB signaling pathway in the intrahepatic cholangiocyte inflammation model of rats,and to explore the ameliorative effects and possible mechanisms of alleviating intrahepatic cholangiocyte inflammation.Methods:45 SD rats were divided into nine groups according to the complete randomization method,with 5 rats in each group:the blank group,the model group,the Dahuang Lingxian Granules group,the NF-κB group,the p38MAPK group,the NF-κB+p38MAPK group,the NF-κB+Dahuang Lingxian Granules group,the p38MAPK+Dahuang Lingxian Granules group,the NF-κB+p38MAPK+Dahuang Lingxian Granules group.Except for the blank group,rats in the remaining groups were injected with 5 mg/kg LPS into the common bile duct to prepare an intrahepatic bile duct inflammation model.After the intragastric admin-istration on the 7th day,the rat bile duct tree was removed,and HE staining was used to observe the degree of inflammation.Western blotting and real-time fluorescence quantitative PCR were used to detect the protein and mRNA expression of IKKα,ASK1,MKK3,and CX3CL1.Results:HE pathology results showed that the inflammation of intrahepatic bile duct tissue and cells in the model group was obvious.After adding Dahuang Lingxian Granules and signal blockers,the inflammation status of in-trahepatic bile ducts was improved compared with before,and the difference in total pathological scores was statistically significant(P<0.05).Compared with the model group,Dahuang Lingxian granules group,p38MAPK group,NF-κB group,NF-κB+p38MAPK group,NF-κB+Dahuang Lingxiang ranules group,p38MAPK+Dahuang Lingxian granules group,NF-κB+p38MAPK+Dahuang Ling The protein and mRNA expression of ASK1 and CX3CL1 in the Xian Granule group decreased,the expression of MKK3 mRNA increased,and the expression of IKKα in the p38MAPK group and NF-κB+MKK3 protein in the Da-huang Lingxian Granule group increased(P<0.05).Compared with the Dahuang Lingxian Granules group,The expression of ASK1 and CX3CL1 mRNA decreased in the p38MAPK group,the NF-κB group,the NF-κB+p38MAPK group,the p38MAPK+Dahuang Lingxian Granules group,the NF-κB+Dahuang Lingxian Granules group,the NF-κB+p38MAPK+Da-huang Lingxian Granules group.The expression of MKK3 mRNA in the p38MAPK+Dahuang Lingxian Granules group,NF-κB+Dahuang Lingxian Granules group,and NF-κB+p38MAPK+Dahuang Lingxian Granules group increased(P<0.05).Compared with the Dahuang Lingxian Granules group,the IKKα protein expression in the p38MAPK group decreased,and the ASK1 and MKK3 protein expressions in the NF-κB+Dahuang Lingxian Granules group increased(P<0.05),while the NF-κB+p38MAPK+Dahuang Lingxian Granules group increased.The expression of CX3CL1 protein in the granule group decreased(P>0.05).Conclusion:Dahuang Lingxian Recipe can alleviate the LPS-induced intrahepatic bile duct inflammatory reaction in rats and promote the repair of bile duct cells,thereby achieving the purpose of reducing the occurrence and postoperative recurrence of PIS.Its mechanism of action may be related to inhibiting the NF-κB/MAPK signaling pathway.It is related to the activation of key in-flammatory factors such as IKKα,ASK1,MKK3 and CX3CL1.

关键词

大黄灵仙方/胆管炎症/IKKα/ASK1/MKK3/CX3CL1

Key words

Dahuang lingxian formula/Bile duct inflammation/IKKα/ASK1/MKK3/CX3CL1

分类

医药卫生

引用本文复制引用

庞浇安,李承积,俞渊,付军,叶桂源,陈伟棠,罗艳萍,滕金豪,刘春丽,肖丽君..大黄灵仙方调控肝内胆管细胞炎症大鼠的作用及机制研究[J].海南医学院学报,2024,30(16):1201-1209,9.

基金项目

This study was supported by National Natural Science Foundation of China(82360889) (82360889)

Natural Science Foundation of Guangxi(2020GXNSFAA238012) (2020GXNSFAA238012)

2024"Qihuang Project"High-Level Talent Team Cultivation Project of TCM and Western Medicine Prevention and Treatment Of Hepatobiliary Related Diseases Research Team(202411) (202411)

2020 Hospital-level Doctoral Project of the First Affiliated Hospital of Guangxi University of Chinese Medicine(2020BS004) (2020BS004)

2020 Introduction of Doctoral Research Start-up Fund Project of Guangxi University of Traditional Chinese Medicine(2020BS030) (2020BS030)

Graduate Education Innovation Program of Guangxi University of Traditional Chinese Medicine(YCSY2023035)国家自然科学基金资助项目(82360889) (YCSY2023035)

广西自然科学基金(2020GXNSFAA238012) (2020GXNSFAA238012)

2024"岐黄工程"高层次人才团队培育项目 肝胆相关疾病的中西医防治研究团队(202411) (202411)

2020年广西中医药大学第一附属医院院级博士启动基金项目(2020BS004) (2020BS004)

2020 年广西中医药大学引进博士科研启动基金项目(2020BS030) (2020BS030)

广西中医药大研究生教育创新计划项目(YCSY2023035) (YCSY2023035)

海南医学院学报

OA北大核心CSTPCD

1007-1237

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