[1]江 东,徐长亮,沈卫星,等.参白解毒方对溃疡性结肠炎肠黏膜上皮细胞保护作用机制研究[J].陕西中医,2022,(1):23-27.[doi:DOI:10.3969/j.issn.1000-7369.2022.01.005]
 JIANG Dong,XU Changliang,SHEN Weixing,et al.Explore protective mechanism of Shenbai Jiedu decoction on colon epithelial cells of ulcerative colitis[J].,2022,(1):23-27.[doi:DOI:10.3969/j.issn.1000-7369.2022.01.005]
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参白解毒方对溃疡性结肠炎肠黏膜上皮细胞保护作用机制研究
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《陕西中医》[ISSN:1000-7369/CN:61-1281/TN]

卷:
期数:
2022年1期
页码:
23-27
栏目:
基础研究
出版日期:
2022-01-05

文章信息/Info

Title:
Explore protective mechanism of Shenbai Jiedu decoction on colon epithelial cells of ulcerative colitis
作者:
江 东1徐长亮2沈卫星2程海波2
(1.南京中医药大学第一临床医学院,江苏 南京 210023; 2.江苏省中医药防治肿瘤协同创新中心 国家中医药管理局名医验方评价与转化重点实验室,江苏 南京 210023)
Author(s):
JIANG DongXU ChangliangSHEN WeixingCHENG Haibo
(The First Clinical College of Nanjing University of Chinese Medicine,Nanjing 210023,China)
关键词:
溃疡性结肠炎 炎症性肠病 癌前病变 参白解毒方 癌毒 结直肠黏膜上皮细胞 细胞周期 细胞增殖
Keywords:
Ulcerative colitis Inflammatory bowel disease Precancerous lesions Shenbai Jiedu decoction Cancer toxin Colorectal mucosal epithelial cells Cell cycle Cell proliferation
分类号:
R 574.62
DOI:
DOI:10.3969/j.issn.1000-7369.2022.01.005
文献标志码:
A
摘要:
目的:研究参白解毒方(SBJDF)对溃疡性结肠炎肠黏膜上皮细胞的保护作用及机制。方法:使用葡聚糖硫酸钠(DSS)刺激人正常结直肠黏膜上皮细胞(FHC),模拟溃疡性结肠炎黏膜上皮细胞的损伤,倒置显微镜观察参白解毒方对PHC损伤模型细胞形态的影响通过MTT法检测DSS对细胞活力的影响,5-乙炔基-2'-脱氧尿苷(EdU)检测参白解毒方对细胞增殖能力的影响,流式细胞仪检测FHC细胞的周期分布变化,通过蛋白免疫印迹法检测细胞周期相关蛋白Cyclin A2、CDK1的表达。结果:DSS能够抑制FHC细胞活力,下调FHC细胞的Cyclin A2、CDK1蛋白表达,将FHC细胞周期阻滞于G0/G1期,抑制细胞增殖; 参白解毒方给药后能减少DSS细胞毒性,增加FHC细胞的Cyclin A2、CDK1蛋白表达,进而逆转DSS导致的FHC细胞G0/G1期阻滞,增加细胞活力。结论:参白解毒方可能通过维持细胞周期稳态发挥对溃疡性结肠炎肠黏膜上皮细胞的保护作用。
Abstract:
Objective:To explore the protective mechanism of Shenbai Jiedu decoction(SBJDF)on ulcerative colitis.Methods:Dextran sodium sulfate(DSS)was used to stimulate normal fetal human colon(FHC)cells to simulate the ulcerative colitis mucosal epithelial cells.After treatment with SBJDF,cell morphology was observed by inverted microscopy,The MTT assay was used to detect the effect of SBJDF on the cell viability of FHC cells,EdU was used to detect the cell proliferation ability,The cell cycle distribution changes was observed by flow cytometry,The expression levels of proteins Cyclin A2,CDK1 were determined by Western blot analysis.Results:DSS decreased viability of FHC cells,DSS induced FHC cell cycle arrest in G0/G1 phase and down-regulated the expression of Cyclin A2 and CDK1,inhibited cell proliferation.After treatment with DSS,SBJDF can inhibit the decrease of FHC cell viability induced by DSS and reverse the down-regulation of Cyclin A2 and CDK1,thereby alleviate the G0/G1 phase block of FHC cells caused by DSS.Conclusion:SBJDF may protect colorectal mucosa cells from inflammatory bowel disease by maintaining cell cycle homeostasis.

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备注/Memo

备注/Memo:
基金项目:国家重点研发计划项目(2017YFC1700602); 江苏省高校优势学科建设工程资助项目(PAPD)
更新日期/Last Update: 2022-01-09