安徽医药
安徽醫藥
안휘의약
ANHUI MEDICAL AND PHARMACEUTICAL JOURNAL
2015年
2期
239-241
,共3页
MPP+%PC12细胞%伊拉地平%氧化应激%帕金森病
MPP+%PC12細胞%伊拉地平%氧化應激%帕金森病
MPP+%PC12세포%이랍지평%양화응격%파금삼병
MPP+%PC12 cells%isradipine%ROS%Parkinson’ s disease
目的:研究伊拉地平( ISR )对1-甲基-4-苯基吡啶离子( MPP+)损伤的PC12细胞的保护作用及可能机制。方法MPP +处理PC12细胞建立帕金森病细胞模型;4-甲基偶氮唑蓝( MTT)比色法检测细胞存活率;双氯荧光黄乙酸乙酯( DCFH-DA)染色流式细胞术检测细胞内活性氧( ROS)的生成;JC-1染色流式细胞术检测细胞线粒体膜电位( MMP)。结果1 mmol · L-1MPP+处理PC12细胞24 h后能明显抑制细胞生长(P<0.01);降低线粒体膜电位;ROS含量增加。2μmol· L-1伊拉地平预处理后, PC12细胞存活率显著增加( P<0.01);线粒体膜电位升高;ROS生成减少。结论伊拉地平对MPP+损伤的PC12细胞具有保护作用,其作用机制可能与维持线粒体正常膜电位,稳定线粒体功能,阻止线粒体氧化应激发生有关。
目的:研究伊拉地平( ISR )對1-甲基-4-苯基吡啶離子( MPP+)損傷的PC12細胞的保護作用及可能機製。方法MPP +處理PC12細胞建立帕金森病細胞模型;4-甲基偶氮唑藍( MTT)比色法檢測細胞存活率;雙氯熒光黃乙痠乙酯( DCFH-DA)染色流式細胞術檢測細胞內活性氧( ROS)的生成;JC-1染色流式細胞術檢測細胞線粒體膜電位( MMP)。結果1 mmol · L-1MPP+處理PC12細胞24 h後能明顯抑製細胞生長(P<0.01);降低線粒體膜電位;ROS含量增加。2μmol· L-1伊拉地平預處理後, PC12細胞存活率顯著增加( P<0.01);線粒體膜電位升高;ROS生成減少。結論伊拉地平對MPP+損傷的PC12細胞具有保護作用,其作用機製可能與維持線粒體正常膜電位,穩定線粒體功能,阻止線粒體氧化應激髮生有關。
목적:연구이랍지평( ISR )대1-갑기-4-분기필정리자( MPP+)손상적PC12세포적보호작용급가능궤제。방법MPP +처리PC12세포건립파금삼병세포모형;4-갑기우담서람( MTT)비색법검측세포존활솔;쌍록형광황을산을지( DCFH-DA)염색류식세포술검측세포내활성양( ROS)적생성;JC-1염색류식세포술검측세포선립체막전위( MMP)。결과1 mmol · L-1MPP+처리PC12세포24 h후능명현억제세포생장(P<0.01);강저선립체막전위;ROS함량증가。2μmol· L-1이랍지평예처리후, PC12세포존활솔현저증가( P<0.01);선립체막전위승고;ROS생성감소。결론이랍지평대MPP+손상적PC12세포구유보호작용,기작용궤제가능여유지선립체정상막전위,은정선립체공능,조지선립체양화응격발생유관。
Objective To stuty the protective effects of isradipine(ISR) against MPP+-induced injury in PC12 cells.Methods Rat pheochromocytoma(PC12) cells treated with MPP+were used as the cell model of Parkinson’s disease.The cell viability was detected by MTT assay.The mitochondrial transmembrane potential and the cellular ROS level were observed by spectrofluorometry.Results Compared with control group,the cell viability of PC12 cells treated with MPP+1 mmol· L -1 for 24 h was significantly declined,ROS markedly generated and mitochondrial membrane potential was increased.Pretreatment with 2 μmmol· L -1 isradipine increased the cell viability and the MMP,and reduced MPP+-induced intracellular ROS production.Conclusion Isradipine could protect against the MPP+-induced injury,whose protective mechanisms may be related to the maintenance of normal mitochondrial membrane poten-tial,stabilization of mitochondrial function and prevention of mitochondrial oxidative stress.