Department of Anesthesiology, Pharmacology & Therapeutics, University of British Columbia, 2176 Health Sciences Mall, Vancouver, BC, Canada V6T 1Z3.
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):945-54. doi: 10.1016/j.pnpbp.2010.04.024. Epub 2010 May 7.
The therapeutic use of atypical antipsychotics is associated with a high incidence of metabolic side-effects. In the present study we examined the acute effects of both high and low-dose atypical antipsychotic drugs and one typical drug on alterations in glucose and insulin parameters using a rodent model. The effects of administration of clozapine (2mg/kg; 20mg/kg), olanzapine (1.5mg/kg; 15 mg/kg), risperidone (0.5mg/kg; 2.5mg/kg) and haloperidol (0.1mg/kg; 1.0mg/kg) on glucose sensitivity and insulin resistance were determined through HOMA-IR values in fasted rats and glucose clearance during a glucose tolerance test. Acute effects were determined 60, 180 or 360 min following drug administration. The atypical antipsychotics produced significant dose and time dependent effects on fasting plasma glucose and insulin concentrations, HOMA-IR values, insulin resistance and glucose intolerance. The greatest effect on glucose dysregulation was noted primarily with clozapine and olanzapine; however, all four treatments caused significant increases in fasting glucose and/or insulin levels with the high dose, 60 min post-drug administration. Together, these findings indicate that acute administration of antipsychotic drugs has potent effects on metabolic regulation of glucose and insulin sensitivities, which may contribute to metabolic side-effects seen in humans.
非典型抗精神病药物的治疗用途与代谢副作用的高发率有关。在本研究中,我们使用啮齿动物模型检查了高剂量和低剂量非典型抗精神病药物以及一种典型药物对葡萄糖和胰岛素参数变化的急性影响。通过空腹大鼠的 HOMA-IR 值和葡萄糖耐量试验期间的葡萄糖清除率,确定氯氮平(2mg/kg;20mg/kg)、奥氮平(1.5mg/kg;15mg/kg)、利培酮(0.5mg/kg;2.5mg/kg)和氟哌啶醇(0.1mg/kg;1.0mg/kg)对葡萄糖敏感性和胰岛素抵抗的影响。急性作用在给药后 60、180 或 360 分钟确定。非典型抗精神病药对空腹血糖和胰岛素浓度、HOMA-IR 值、胰岛素抵抗和葡萄糖耐量有显著的剂量和时间依赖性影响。氯氮平和奥氮平对血糖失调的影响最大;然而,所有四种治疗方法在高剂量时,即给药后 60 分钟,均导致空腹血糖和/或胰岛素水平显著升高。这些发现表明,抗精神病药物的急性给药对葡萄糖和胰岛素敏感性的代谢调节有强烈影响,这可能导致人类出现代谢副作用。