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熊果酸对H22荷瘤小鼠抗肿瘤及免疫调节作用
引用本文:李艳红,李晓波,陆雪莹,高剑峰,肖向文.熊果酸对H22荷瘤小鼠抗肿瘤及免疫调节作用[J].实验动物科学,2013(5):1-5,14.
作者姓名:李艳红  李晓波  陆雪莹  高剑峰  肖向文
作者单位:[1]石河子大学动物科技学院,石河子832003 [2]中国科学院新疆理化技术研究所干旱区植物资源化学重点实验室,乌鲁木齐830011
基金项目:新疆维吾尔自治区自然科学基金(No.2011211B51);中国科学院资源环境科学与技术局重要创新方向“西部行动”项目(KZCX-XB2-17)
摘    要:目的 探讨熊果酸(UA)对H22荷瘤小鼠抗肿瘤作用及免疫功能的影响.方法 皮下移植建立H22荷瘤小鼠模型,腹腔注射不同剂量UA,检测抑瘤率和免疫器官指数,MTT法检测脾脏T、B淋巴细胞增殖能力,流式细胞术检测CD4+、CD8+T细胞亚群含量及比例,ELISA法检测血清细胞因子IL-2、IL-4和TNF-α的表达量.结果 UA对小鼠皮下移植性肿瘤H22有显著的抑制作用,可降低免疫器官中异常增大的脾指数,增强脾脏中T、B淋巴细胞增殖能力,提高淋巴细胞亚群CD4+T细胞表达及CD4+/CD8+T细胞亚群比例,促进血清IL-2、TNF-α表达,降低IL-4表达.结论 UA可抑制小鼠肝癌H22肿瘤生长,体内可以提高荷瘤小鼠的免疫能力,其抗肿瘤作用可能与机体的免疫调节作用相关.

关 键 词:熊果酸  小鼠肝癌H22细胞  抑瘤率  免疫调节

Antitumor Effect and Immune Regulation Activity of Ursolic Acid on Hepatoma H22 in Mice
LI Yan-hong,LI Xiao-bo,LU Xue-ying,GAO Jian-feng,XIAO Xiang-wen.Antitumor Effect and Immune Regulation Activity of Ursolic Acid on Hepatoma H22 in Mice[J].Shiyan Dongwu Kexue,2013(5):1-5,14.
Authors:LI Yan-hong  LI Xiao-bo  LU Xue-ying  GAO Jian-feng  XIAO Xiang-wen
Affiliation:1.College of Animal Science and Technology, Shihezi University, Shihezi 832003, China;Key Laboratory of Chemistry of Plant Resources in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry,Chinese Academy of Sciences, Urumqi 830011, China;)
Abstract:Objective The aim of this study was to investigate the antitumor effect and immune regulation activity of Ursolic acid (UA) on H22 in mice.Method The models of tumor-bearing mice were established by i.p.injection of hepatic cancer H22 and the mice were randomly divided into 5 groups,each groups given by i.p.The tumor inhibitory rate,the thymus index and spleen index were calculated,lymphocyte proliferation of spleen stimulated by ConA and LPS were detected by MTT,T cell subsets CD4+,CD8 + were detected by FCM and the levels of The cytokine IL-2,TNF-α,IL-4 in serum were detected by ELISA.Result In vivo,the inhibitory rate of UA significantly higher than that of the model group.Compared with the model group,spleen index of high dose UA group were significantly lower.The T and B lymphocyte proliferation of spleen were significantly higher.The CD4 +T cell subset and CD4 +/CD8 +T rate were significantly increased,but CD8 +T cells has no significant change.The cytokine IL-2,TNF-oα in serum expression were promoted with high dose UA,meanwhile the IL-4 expression was reduced.Conclusion The results show that UA can inhibit tumor growth both in vitro and in vivo.It could play a role of antitumor activity in vivo by regulating the body's abnormal immune function in tumor-bearing mice.
Keywords:ursolic acid  hepatocellular carcinoma cell line of mice (H22)  inhibiting tumor rate  immune regulation
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