通过阻断K(ATP)通道调节1-甲基-4-苯基吡啶鎓诱导的PC12细胞线粒体功能障碍和细胞死亡。
Modulation of 1-methyl-4-phenylpyridinium-induced mitochondrial dysfunction and cell death in PC12 cells by K(ATP) channel block.
作者信息
Lee C S, Kim Y J, Ko H H, Han E S
机构信息
Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul, South Korea.
出版信息
J Neural Transm (Vienna). 2007 Mar;114(3):297-305. doi: 10.1007/s00702-006-0594-3. Epub 2006 Nov 17.
The present study investigated the effect of 5-hydroxydecanoate, a selective mitochondrial K(ATP) channel blocker, on the cytotoxicity of neurotoxin 1-methyl-4-phenylpyridinium (MPP(+)) in differentiated PC12 cells. 5-Hydroxydecanoate and glibenclamide (a cell surface and mitochondrial K(ATP) channel inhibitor) reduced the MPP(+)-induced cell death and GSH depletion and showed a maximal inhibitory effect at 5 and 10 microM, respectively. Addition of 5-hydroxydecanoate attenuated the MPP(+)-induced nuclear damage, changes in the mitochondrial membrane permeability and increase in the reactive oxygen species formation in PC12 cells. The results show that 5-hydroxydecanote may prevent the MPP(+)-induced viability loss in PC12 cells by suppressing formation of the mitochondrial permeability transition, leading to the cytochrome c release and caspase-3 activation. This effect appears to be accomplished by the inhibitory action on the formation of reactive oxygen species and the depletion of GSH. The blockade of mitochondrial K(ATP) channels seems to prevent the MPP(+)-induced neuronal cell damage.
本研究调查了选择性线粒体ATP敏感性钾通道阻滞剂5-羟基癸酸对分化型PC12细胞中神经毒素1-甲基-4-苯基吡啶离子(MPP⁺)细胞毒性的影响。5-羟基癸酸和格列本脲(一种细胞表面和线粒体ATP敏感性钾通道抑制剂)减少了MPP⁺诱导的细胞死亡和谷胱甘肽耗竭,分别在5和10微摩尔时显示出最大抑制作用。添加5-羟基癸酸可减轻MPP⁺诱导的PC12细胞核损伤、线粒体膜通透性变化以及活性氧生成增加。结果表明,5-羟基癸酸可能通过抑制线粒体通透性转换的形成来防止MPP⁺诱导的PC12细胞活力丧失,从而导致细胞色素c释放和半胱天冬酶-3激活。这种作用似乎是通过对活性氧形成的抑制作用和谷胱甘肽的耗竭来实现的。线粒体ATP敏感性钾通道的阻断似乎可以防止MPP⁺诱导的神经元细胞损伤。