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The effects of ziprasidone, clozapine and haloperidol on lipid peroxidation in human plasma (in vitro): Comparison

机译:齐拉西酮、氯氮平和氟哌啶醇对人血浆脂质过氧化的影响(体外):比较

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摘要

Oxidative injury in schizophrenia can be caused by the disease itself and probably by antipsychotics treatment. The aim of the study was to establish whether there is a difference between ziprasidone, clozapine and haloperidol effect on lipid peroxidation in human plasma, measured by the level of thiobarbituric acid reactive substances (TBARS). The samples of plasma from healthy subjects were incubated with the drugs (1 and 24 h) and compared with control samples. The levels of TBARS were measured spectrophotometrically, according to the Rice-Evans method. The multifactorial variance analysis ANOVA II test showed that the differences in TBARS levels significantly depended on the studied drugs (ziprasidone 40 ng/ml, haloperidol 4 ng/ml and clozapine 350 ng/ml) (F = 3.248 p = 0.047) and (ziprasidone 139 ng/ml, haloperidol 20 ng/ml and clozapine 420 ng/ml) (F = 2.248, p = 2.9 × 10-5). Statistically increased levels of TBARS after 24 h incubation of plasma with ziprasidone 139 ng/ml and haloperidol 20 ng/ml (p 0.05) increase TBARS level in plasma in comparison with control samples. The results obtained in the study showed that ziprasidone and haloperidol contrary to clozapine induced a significant increase in plasma lipid peroxidation.
机译:精神分裂症的氧化损伤可由疾病本身引起,也可能由抗精神病药物治疗引起。该研究的目的是确定齐拉西酮、氯氮平和氟哌啶醇对人血浆中脂质过氧化的影响是否存在差异,通过硫代巴比妥酸反应物质 (TBARS) 的水平来衡量。将来自健康受试者的血浆样品与药物一起孵育(1和24小时),并与对照样品进行比较。根据Rice-Evans方法,用分光光度法测量TBARS的水平。多因素方差分析方差分析 II 检验显示,TBARS 水平的差异显着取决于所研究药物(齐拉西酮 40 ng/ml、氟哌啶醇 4 ng/ml 和氯氮平 350 ng/ml)(F = 3.248 p = 0.047)和(齐拉西酮 139 ng/ml、氟哌啶醇 20 ng/ml 和氯氮平 420 ng/ml)(F = 2.248、p = 2.9 × 10-5)。与对照样品相比,观察到用齐拉西酮 139 ng/ml 和氟哌啶醇 20 ng/ml(分别为 p 0.05)增加血浆中的TBARS水平。研究结果显示,与氯氮平相反的齐拉西酮和氟哌啶醇诱导血浆脂质过氧化的显着增加。

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