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作 者:李成冲[1,2] 李佳鸣[1,2] 王刚[1,2] 邹德佳[1,2] 耿玉涛[1,2] 李强[1] 牛英才[1]
机构地区:[1]齐齐哈尔医学院医药科学研究所,黑龙江齐齐哈尔161042 [2]佳木斯大学化学与药学院,黑龙江省生物药制剂重点实验室,黑龙江佳木斯154007
出 处:《中国实验方剂学杂志》2010年第9期134-137,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:黑龙江省自然科学基金项目(ZA2006-1);黑龙江省教育厅科学技术研究面上项目(11541413)
摘 要:目的:探讨镇肝熄风汤载药脑脊液对甲基-苯基-吡啶离子(1-methyl-4-phenylpyridinium,MPP+)诱导的PC12细胞损伤的保护作用。方法:不同浓度的镇肝熄风汤载药脑脊液预处理体外培养的PC12细胞后,加入MPP+诱导PC12细胞损伤模型。用MTT法检测PC12细胞活力,实时定量PCR检测Bax和Bcl-2 mRNA的表达,Western blot检测Bax和Bcl-2蛋白表达。结果:MPP+处理72~96 h,与空白对照组比较,模型组细胞活力明显降低,Bcl-2 mRNA和蛋白表达显著下调,Bax mRNA和蛋白表达显著上调(P<0.05)。与模型组比较,不同浓度的镇肝熄风汤载药脑脊液细胞活力明显升高,Bcl-2 mRNA和蛋白表达显著上调,Bax mRNA和蛋白表达显著下调,差异具有统计学意义(P<0.05)。结论:镇肝熄风汤载药脑脊液对MPP+诱导的PC12细胞具有保护作用,可能是通过上调Bcl-2和下调Bax的mRNA和蛋白表达而发挥抑制PC12细胞凋亡的作用。Objective:To investigate the protective effect of cerebrospinal fluid containing Zhenganxifeng decoction(CSF-ZGXF) on pc12 cell induced by 1-methyl-4-phenylpyridinium ion(MPP +).Method:Neurotoxicity was induced by addition of MPP + into PC12 cell cultures.And different doses of CSF-ZGXF were administrated 24 h before addition of MPP + into PC12 cell cutrure.Cell viability,mRNA and protein of Bax and Bcl-2 expression was assayed by MTT,real-time PCR and western blot.Result:Optical density for PC12 cells treated with MPP + for 48-96 h was lower than that of the control group.The mRNA and protein expression of Bcl-2 was down-regulated and those of Bax was up-regulated in MPP + groups compared with the control group.The mRNA and protein expression of Bcl-2 were up-regulated and those of Bax were down-regulated in CSF-ZGXF group compared with the MPP + group.Conclusion:The results suggest that protective effect of CSF-ZGXF on PC12 cells may correlate with downregulation of mRNA and protein expression of Bax and up-regulation of those of Bcl-2.
关 键 词:帕金森病 镇肝熄风汤 载药脑脊液 1-甲基-4-苯基吡啶离子 细胞凋亡
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