抗抑郁药对分化的PC12细胞中1-甲基-4-苯基吡啶鎓毒性显示出不同的作用。
Antidepressants reveal differential effect against 1-methyl-4-phenylpyridinium toxicity in differentiated PC12 cells.
作者信息
Han Young Su, Lee Chung Soo
机构信息
Department of Pharmacology, College of Medicine, Chung-Ang University, Seoul 156-756, South Korea.
出版信息
Eur J Pharmacol. 2009 Feb 14;604(1-3):36-44. doi: 10.1016/j.ejphar.2008.12.025. Epub 2008 Dec 24.
Treatment of depression may ameliorate the cognitive disability and motor slowness in Parkinson's disease. It has been shown that antidepressants, including fluoxetine, may attenuate or exacerbate neuronal cell death. The present study assessed the effect of antidepressants (amitriptyline, tranylcypromine and fluoxetine) against the toxicity of 1-methyl-4-phenylpyridinium (MPP(+)) in relation to the mitochondria-mediated cell death process in differentiated PC12 cells. Amitriptyline and tranylcypromine attenuated the MPP(+)-induced cell death that may be associated with mitochondrial membrane permeability change and oxidative stress. Both compounds prevented the loss of the mitochondrial transmembrane potential, over-expression of Bax, reduction in Bcl-2 level, cytochrome c release, caspase-3 activation, formation of reactive oxygen species and depletion of GSH. The inhibitory effect of tranylcypromine was greater than that of amitriptyline on the basis of concentration. In contrast, fluoxetine revealed a toxic effect and exhibited an additive effect against the toxicity of MPP(+). Results show that amitriptyline and tranylcypromine may attenuate the MPP(+) toxicity by suppressing the mitochondrial membrane permeability change that leads to cytochrome c release and subsequent caspase-3 activation. The effects seem to be associated with the inhibitory action on the formation of reactive oxygen species and the depletion of GSH. In contrast, fluoxetine seems to exert an additive toxic effect against neuronal cell damage by increasing mitochondrial damage and oxidative stress.
抑郁症的治疗可能会改善帕金森病的认知障碍和运动迟缓。已有研究表明,包括氟西汀在内的抗抑郁药可能会减轻或加剧神经元细胞死亡。本研究评估了抗抑郁药(阿米替林、反苯环丙胺和氟西汀)对1-甲基-4-苯基吡啶离子(MPP(+))毒性的影响,该毒性与分化的PC12细胞中线粒体介导的细胞死亡过程有关。阿米替林和反苯环丙胺减轻了MPP(+)诱导的细胞死亡,这可能与线粒体膜通透性改变和氧化应激有关。这两种化合物都能防止线粒体跨膜电位的丧失、Bax的过度表达、Bcl-2水平的降低、细胞色素c的释放、半胱天冬酶-3的激活、活性氧的形成以及谷胱甘肽的消耗。基于浓度,反苯环丙胺的抑制作用大于阿米替林。相比之下,氟西汀显示出毒性作用,并对MPP(+)的毒性表现出相加作用。结果表明,阿米替林和反苯环丙胺可能通过抑制线粒体膜通透性改变来减轻MPP(+)毒性,而线粒体膜通透性改变会导致细胞色素c释放及随后的半胱天冬酶-3激活。这些作用似乎与对活性氧形成和谷胱甘肽消耗的抑制作用有关。相比之下,氟西汀似乎通过增加线粒体损伤和氧化应激对神经元细胞损伤产生相加毒性作用。