首页 | 本学科首页   官方微博 | 高级检索  
检索        

艾司西酞普兰对MPTP处理的PC12细胞的保护作用及机制
引用本文:李娜,张君,刘俊骞,张赛,刘惠苗,王文婷,张忠霞,仇福成,顾平.艾司西酞普兰对MPTP处理的PC12细胞的保护作用及机制[J].解剖学杂志,2019,42(1):31-35.
作者姓名:李娜  张君  刘俊骞  张赛  刘惠苗  王文婷  张忠霞  仇福成  顾平
作者单位:河北医科大学第一医院神经内科,石家庄050031;河北医科大学第一医院脑功能科,石家庄050031;河北医科大学第一医院细胞治疗实验室,石家庄,050031;河北医科大学第一医院脑功能科,石家庄,050031;河北医科大学第一医院神经内科,石家庄,050031;河北医科大学第一医院神经内科,石家庄050031;河北省脑老化与认知神经科学实验室,石家庄050031
摘    要:目的 :探讨艾司西酞普兰(ESC)对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的PC12细胞的保护作用及其机制。方法 :用不同浓度ESC或/和不同浓度MPTP处理PC12细胞,再用3-甲基腺嘌呤(3-MA)抑制;通过MTS检测细胞存活率,Hoechst 33258染色观察细胞凋亡,免疫印迹检测自噬标记物LC3B-Ⅱ、LC3B-Ⅰ和凋亡蛋白Bcl-2、Bax的表达。结果 :经筛选得出,10μmol/L ESC预处理PC12细胞1 h,再加入1 000μmol/L MPTP处理24 h,细胞存活率显著提高;Hoechst 33258染色显示细胞核固缩明显减少;ESC+MPTP组LC3B-Ⅱ/Ⅰ、Bcl-2/Bax表达水平较MPTP组显著上升,但ESC+MPTP+3MA组LC3B-Ⅱ/Ⅰ、Bcl-2/Bax表达水平均显著下降。结论 :ESC对MPTP处理的PC12细胞有一定的神经保护作用,可能通过PI3K/Akt途径激发自噬作用,提高了Bcl-2的表达,抑制MPTP引发的细胞凋亡,从而发挥对其保护作用。

关 键 词:帕金森病  艾司西酞普兰  自噬  PC12细胞  1-甲基-4-苯基-1  2  3  6-四氢吡啶  3-甲基腺嘌呤

Protective effect and mechanism of estalopram on PC12 cells treated with MPTP
Li Na,Zhang Jun,Liu Junqian,Zhang Sai,Liu Huimiao,Wang Wenting,Zhang Zhongxia,Qiu Fucheng,Gu Ping.Protective effect and mechanism of estalopram on PC12 cells treated with MPTP[J].Chinese Journal of Anatomy,2019,42(1):31-35.
Authors:Li Na  Zhang Jun  Liu Junqian  Zhang Sai  Liu Huimiao  Wang Wenting  Zhang Zhongxia  Qiu Fucheng  Gu Ping
Institution:(Department of Neurology,First Hospitalof Hebei Medical University,Shijiazhuang 050031,China;Cell Therapy Laboratory,First Hospitalof Hebei Medical University,Shijiazhuang 050031,China;Department of Brain Function,First Hospitalof Hebei Medical University,Shijiazhuang 050031,China;Brain Aging and Cognitive Neuroscience Laboratory of Hebei Province,First Hospitalof Hebei Medical University,Shijiazhuang 050031,China)
Abstract:Objective:To investigate the protective effect and mechanism of estalopram(ESC)on PC12 cells treated with 1-methyl-4-phenyl-6-tetrahydropyridine(MPTP).Methods:PC12 cells were treated with different concentrations of ESC or/and MPTP and then inhibited by 3-methyladenine(3-MA).The cell viability rate was detected by MTS.Cell apoptosis was detected by Hoechst 33258 staining.The expression of autophagy marker LC3B-Ⅱ,LC3B-Ⅰand apoptotic protein Bcl-2,Bax were detected by Western blotting.Results:PC12 cells were pretreated with 10μmol/L ESC for 1 h,and then treated with 1 000μmol/L MPTP for 24 h.The cell viability rate was significantly increased.Hoechst 33258 staining showed that nuclear pyknosis was significantly decreased.The expression of LC3B-Ⅱ/Ⅰand Bcl-2/Bax in ESC+MPTP group was significantly higher than that in MPTP group,but the expression of LC3B-Ⅱ/Ⅰand Bcl-2/Bax in ESC+MPTP+3MA group was significantly lower than that in MPTP group.Conclusion:ESC has a neuroprotective effect on PC12 cells treated with MPTP,which may stimulate autophagy through PI3K/Akt pathway,increase the expression of Bcl-2 and inhibit the apoptosis induced by MPTP.
Keywords:Parkinson's disease  escitalopram  autophagy  PC12 cell  1-methyl-4-phenyl-1-trimethyl-6-tetrahydropyridine  3-methyladenine
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《解剖学杂志》浏览原始摘要信息
点击此处可从《解剖学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号