Yang Ming-Chang, Chen Kun-Po, Lung For-Wey
Department of Psychiatry, Kaohsiung Armed Forces General Hospital, Kaohsiung City, Taiwan, ROC; Institute of Biological Science, National Sun Yat-sen University, Kaohsiung City, Taiwan, ROC.
Taipei City Hospital, Songde Branch, Taipei, Taiwan, ROC.
Eur J Pharmacol. 2014 Oct 5;740:697-702. doi: 10.1016/j.ejphar.2014.06.007. Epub 2014 Jun 21.
A comparison of the neuroprotective effect of different antipsychotics (APDs) over time on naïve SH-SY5Y against oxidative stressor insults using the generalized estimating equation (GEE). The hydrogen peroxide (H2O2), N-methyl-4-phenylpyridinium ion (MPP+), and β-amyloid peptide were used to treat cells with or without APDs (paliperidone, risperidone, olanzapine and haloperidol); cell survival and oxidative stress markers were measured and analyzed. Only haloperidol had higher baseline cytotoxicity than paliperidone. GEE showed the proper exposure time for evaluating the neuroprotection of APDs was 24 h, rather than 48 or 72 h. Paliperidone was superior to other APDs in protecting naïve SH-SY5Y, had the best effect against H2O2-, MPP+-induced cell death, and caused a significantly higher GST, lower HNE and protein carbonyl productions of naïve SH-SY5Y after stressor insults, which may implicate a molecular mechanism underlying its neuroprotective action. Repeated GEE measurements can correct for the correlation among the clusters to obtain a more accurate result for evaluating drug outcome. The interaction between drugs and stressors should be taken into account when determining the neuroprotective effect of APDs against different stressors. Paliperidone might be useful in alleviating oxidative stress induced by Aβ25-35 and MPP+, and provide neuroprotection against hydrogen peroxide in naïve SH-SY5Y.
使用广义估计方程(GEE)比较不同抗精神病药物(APD)对未处理的SH-SY5Y细胞随时间推移针对氧化应激源损伤的神经保护作用。用过氧化氢(H2O2)、N-甲基-4-苯基吡啶离子(MPP+)和β-淀粉样肽处理有或没有APD(帕利哌酮、利培酮、奥氮平和氟哌啶醇)的细胞;测量并分析细胞存活率和氧化应激标志物。只有氟哌啶醇的基线细胞毒性高于帕利哌酮。GEE显示评估APD神经保护作用的合适暴露时间为24小时,而非48或72小时。在保护未处理的SH-SY5Y细胞方面,帕利哌酮优于其他APD,对H2O2、MPP+诱导的细胞死亡效果最佳,并且在应激源损伤后,使未处理的SH-SY5Y细胞的谷胱甘肽S-转移酶(GST)显著升高、4-羟基壬烯醛(HNE)和蛋白质羰基产物降低,这可能暗示了其神经保护作用的分子机制。重复的GEE测量可以校正聚类之间的相关性,以获得更准确的评估药物效果的结果。在确定APD对不同应激源的神经保护作用时,应考虑药物与应激源之间的相互作用。帕利哌酮可能有助于减轻Aβ25-35和MPP+诱导的氧化应激,并为未处理的SH-SY5Y细胞提供针对过氧化氢的神经保护作用。