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机构地区:[1]中国医科大学盛京医院神经内科,辽宁沈阳110004
出 处:《解剖科学进展》2010年第6期527-530,共4页Progress of Anatomical Sciences
摘 要:目的观察KATP通道开放剂吡那地尔对缺血缺氧PC12细胞凋亡的影响,探讨KATP通道开放剂对缺血缺氧PC12细胞凋亡的信号转导机制。方法取传代后3d的PC12细胞,分为正常对照组、缺血对照组、吡那地尔预处理组、吡那地尔+格列吡嗪处理组共4组。采用Annexin-VFITC/PI双染流式细胞分析仪检测凋亡率,应用Western-blotting检测p-CREB蛋白表达水平,观察KATP开放剂对缺血缺氧PC12细胞凋亡的保护作用。结果与缺血对照组相比,吡那地尔预处理组PC12细胞凋亡率明显降低(p<0.05),吡那地尔预处理组PC12细胞p-CREB蛋白表达增加(p<0.05)。结论 KATP通道开放剂吡那地尔能明显降低缺血缺氧后PC12细胞凋亡,增加p-CREB蛋白表达,CREB可能是KATP通道开放剂减少缺血缺氧后PC12细胞凋亡的途径之一。Objective To observe the effect and mechanism of KATP channel opener(pinacidil) on the apoptosis and the PI3K/Akt/CREB signal pathway of PC12 cells induced by ischemia and hypoxia. Methods PC12 cells cultured 3d after passage were divided into: normal control group, ischemic and hypoxia group, pinacidil treatment, pinacidil+glipizide group. Neuronal apoptosis was detected by Annexin-V FITC/PI double-dyed flow cytometry, the expression of p-CREB protein was detected by Western-blotting. Results Compared with ischemic and hypoxia group, the apoptosis rate of PC12 cells decreased(P〈0.05) and the expression level of p-CREB protein in PC12 cells increased (P〈0.05) in pinacidil treated group. Conclusion The decrease of PC12 cells apoptosis and increase of p-CREB protein expression by pinacidil indicate that CREB might be related to the inhibitory mechanism of apoptosis in hypoxia-ischemia PC12 cells by pinacidil.
关 键 词:吡那地尔 ATP敏感性钾通道 PC12细胞 凋亡 P-CREB
分 类 号:R743.31[医药卫生—神经病学与精神病学]
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