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肌酐代谢产物对人肾小管上皮细胞毒性作用的比较研究
引用本文:杨波,邓薇,蒋云生,段绍斌,谢红萍,赵欢顺,关理.肌酐代谢产物对人肾小管上皮细胞毒性作用的比较研究[J].中国医师杂志,2011,13(6):738-741.
作者姓名:杨波  邓薇  蒋云生  段绍斌  谢红萍  赵欢顺  关理
作者单位:1. 南华大学附属第一医院肾内科,湖南省衡阳,421001
2. 中南大学湘雅二医院肾内科
摘    要:目的比较观察甲基胍、1。甲脲乙醇酸酐对人肾小管上皮细胞的毒性作用。方法HK.2细胞作为研究对象,分为三组培养:正常对照(A)组,甲基胍(B)组、1-甲脲乙醇酸酐(C)组,用MTr比色试验法检测细胞增殖,NAG酶释放检测对细胞的毒性,Hoechst染色及AnnexinV—FITC/PI流式细胞术检测凋亡。结果HK-2细胞加入甲基胍、1-甲脲乙醇酸酐后,较正常对照组吸光度值显著下降(0.188±0.011,0.176±0.010VS0.545±0.021,F=1557.74,P〈0.01),NAG酶浓度显著上升(20.488±0.473,22.225±0.565VS5.1254-0.198,F:3848.22,P〈0.01)。Hoechst33258染色显示凋亡细胞呈现核固缩,染色加深,并出现凋亡小体。流式细胞术显示B组、C组HK-2细胞凋亡率显著高于A组(18.23±1.1581,20.22±1.1433VS2.4734-0.321,F=526.06,P〈0.01)。C组吸光度值显著低于B组(0.176±0.010VS0.1884-0.011,t=2.26,P〈0.05),NAG酶浓度显著高于B组(22.225±0.565VS20.488±0.473,t=-6.67.P〈0.01),凋亡率显著高于B组(20.224-1.1433VS18.23±1.1581,t=-2.762,P〈0.05)。结论1.甲脲乙醇酸酐对肾小管上皮细胞的毒性作用强于甲基胍。

关 键 词:甲基胍/副作用  肌酸酐/副作用  肾小管/细胞学  上皮细胞/药物作用/病理学

The study of cytotoxic effect to creatinine metabolite on HK-2 cells in vitro
YANG Bo,DENG Wei,JIANG Yun-sheng,DUAN Shao-bin,XIE Hong-ping,ZHAO Huang-sun,GUAN Li.The study of cytotoxic effect to creatinine metabolite on HK-2 cells in vitro[J].Journal of Chinese Physician,2011,13(6):738-741.
Authors:YANG Bo  DENG Wei  JIANG Yun-sheng  DUAN Shao-bin  XIE Hong-ping  ZHAO Huang-sun  GUAN Li
Institution:. * Department of Nephrology, the First AJfiliated Hospital of Nanhua University, Hengyang 420001, China
Abstract:Objective To investigate the effect of methylguanidine and 1-methylhydantoin on cells cytotoxicity, apoptosis in human renal tubular epithelial cell line (HK-2). Methods Human PTEC cell line HK-2 was used in this study. HK-2 was cultured and divided into 3 groups: Norma1 control group (A), methylguanidine group(B) and 1-methylhydantoin group (C). The cell inhibitory rate of HK-2 was detected by MTT method. The cytotoxicity of methylguanidine to HK-2 was determined by NAG release test. Cell apoptosis was evaluated by using Hoechst stain and FACS with Annexin-V/PI. Results The OD value and NAG concentration of creatinine, methylguanidine and 1-methylhydantoin group were compared with normal control group. OD value decreased and NAG concentration significantly increased(0.188±0.011, 0.176±0.010 vs 0.545±0.021, F=1557.74, P<0.01; 20.488±0.473, 22.225±0.565 vs 5.125±0.198, F=3848.22, P<0.01). By Hoechst stain, pycnosis and apoptotic body could be found when HK-2 was cultivated in methylguanidine 1-methylhydantoin group. In methylguanidine, 1-methylhydantoin group apoptotic HK-2 apparently increased, compared with that in control group (18.23±1.1581, 20.22±1.1433 vs 2.473±0.321, F=526.06, P<0.01). Compared with group B, the OD value in group C decreased significantly (0.176±0.010 vs 0.188±0.011,t=2.26, P<0.05), NAG concentration increased significantly (22.225±0.565 vs 20.488±0.473,t=-6.67, P<0.01), and apoptotic rate in-creased significantly (20.22±1.1433 vs 18.23±1.1581,t=-2.762, P<0.05). Conclusions 1-methylhydantoin has more powerful cytotoxic effect to renal tubular epithelial cells than that of Methylguanidine.
Keywords:Methylguanidine/AE  Creatinine/AE  Kidney tubules/CY  Epithelial cells/DE/PA
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