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首页|期刊导航|中药药理与临床|枳术丸中饮片炮制前后成分变化及抗溃疡性结肠炎损伤的作用机制

枳术丸中饮片炮制前后成分变化及抗溃疡性结肠炎损伤的作用机制

杨青松 高增祥 黄鹏 余学成 涂济源 刘艳菊 曹国胜 苏文龙

中药药理与临床2026,Vol.42Issue(5):15-24,10.
中药药理与临床2026,Vol.42Issue(5):15-24,10.

枳术丸中饮片炮制前后成分变化及抗溃疡性结肠炎损伤的作用机制

Changes in Components of ZhizhuPill before and after Processing and Mechanism of Its Anti-UC Damage

杨青松 1高增祥 1黄鹏 1余学成 1涂济源 1刘艳菊 1曹国胜 1苏文龙1

作者信息

  • 1. 湖北中医药大学药学院,武汉 430065
  • 折叠

摘要

Abstract

Objective:To elucidate the therapeutic mechanism of Zhizhu Pill(枳术丸)in treating ulcerative colitis(UC)through a combination of chemical analysis,network pharmacology,molecular docking,and animal experimentation and to preliminarily explore its therapeutic material basis and action targets.Methods:The chemical constituents and se-rum components of both raw and processed Zhizhu Pill were identified using UPLC-Q-Exactive MS2 technology to identify the blood components.Potential therapeutic targets were predicted using the SwissTargetPrediction and Genecards data-bases,and the"drug-component-target-disease"and"pathway-target-blood component"networks were constructed.Pro-tein-protein interaction(PPI)networks were generated via the STRING database.Functional enrichment analyses,inclu-ding Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG),were conducted using the David database,with molecular docking employed for validation.For animal experimentation,56 Balb/c mice were randomly di-vided into a normal control group,a model control group,9 g/kg and 18 g/kg raw Zhizhu Pill groups,9 g/kg and 18 g/kg processed Zhizhu Pill groups,and a 0.25 g/kg sulfasalazine(SASP)group.The mice were fed for 3 days for acclimation.The normal control group was fed with normal diet and water,and the other groups were free to drink 3.5%DSS solution.During modeling,the normal control group and the model control group were given normal saline by ga-vage,and each medication group was given the corresponding drug by gavage for 7 days.The effects of Zhizhu Pill on co-lon length,disease activity index(DAI)score,and intestinal mucosal injury were observed.The pathological changes in the colon,as well as the number of goblet cells,were assessed using hematoxylin and eosin(HE)staining and Alcian blue-periodic acid Schiff(AB-PAS)staining.Terminal deoxynucleotidyl transferase dUTP nick end labeling(TUNEL)staining was used to detect apoptosis in colon epithelial cells,and Western blot analysis was performed to analyze the ex-pression of apoptosis-related proteins,including cleaved caspase-3,B-cell lymphoma-2(Bcl-2),and Bcl-2-associated X protein(Bax).Results:38 compounds were identified in Zhizhu Pill,of which 18 were prototypical absorbing compo-nents,including 9 flavonoids,3 terpenoids,2 organic acids,and 4 other types of compounds.Network pharmacology anal-ysis showed that isomeranzin,limonin,tangeretin,atractylenolide I,atractylenolide II,and atractylenolide III were potential active ingredients of Zhizhu Pill that could improve UC,and BCL2 and CASPASE-3 were key targets.Molecular docking results showed high affinity of the six key active ingredients to BCL2 and CASPASE-3.The results of animal experiments showed that compared with those in the normal control group,the body weight,colon length,and DAI score of UC mice in the model control group were decreased significantly(P<0.01).In addition,in the model control group,the expression of Bcl-2 protein in colon was significantly downregulated(P<0.01),while the expression of Bax and cleaved caspase-3 was significantly upregulated(P<0.05 or P<0.01).Compared with the model control group,both the raw and processed forms of Zhizhu Pill significantly improved the body weight,colon length,and DAI score of UC mice(P<0.05 or P<0.01),reduced intestinal mucosal injury,and increased goblet cell number.The 18 g/kg processed Zhizhu Pill group exhibited significantly inhibited apoptosis of intestinal epithelial cells(P<0.05),upregulated expression of Bcl-2(P<0.05),and downregulated expression of Bax and cleaved caspase-3(P<0.01).Conclusion:The chemical components of Zhizhu Pill have no obvious change before and after processing.It can significantly improve UC injury,with the pro-cessed product slightly outperforming the raw form.The results of network pharmacology analysis and animal experiment verification show that it plays its therapeutic role against UC probably by regulating the cell apoptosis pathway and reduc-ing mucosal injury.

关键词

枳术丸/溃疡性结肠炎/超高效液相色谱-四极杆-静电场轨道阱高分辨质谱/网络药理学/细胞凋亡

Key words

Zhizhu Pill/Ulcerative colitis/UPLC-Q-exactive MS2/Network pharmacology/Apoptosis

引用本文复制引用

杨青松,高增祥,黄鹏,余学成,涂济源,刘艳菊,曹国胜,苏文龙..枳术丸中饮片炮制前后成分变化及抗溃疡性结肠炎损伤的作用机制[J].中药药理与临床,2026,42(5):15-24,10.

基金项目

湖北省自然科学基金创新发展联合基金项目(编号:2025FAD569) (编号:2025FAD569)

湖北省教育厅科学研究计划指导项目(编号:B2024091). (编号:B2024091)

中药药理与临床

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