Mamo David, Kapur Shitij, Shammi C M, Papatheodorou George, Mann Steve, Therrien François, Remington Gary
Department of Psychiatry, University of Toronto, Montreal, Canada.
Am J Psychiatry. 2004 May;161(5):818-25. doi: 10.1176/appi.ajp.161.5.818.
Ziprasidone is an atypical antipsychotic drug that shows a higher affinity for serotonin 5-HT(2) receptors compared with dopamine D(2) receptors in vitro. The affinity of ziprasidone for these receptors in vivo in patients was examined in a positron emission tomography (PET) study.
The authors conducted a PET study to evaluate D(2) occupancy (using [(11)C]raclopride) and 5-HT(2) occupancy (using [(18)F]setoperone) in brain regions of interest in 16 patients with schizophrenia or schizoaffective disorder randomly assigned to receive 40, 80, 120, or 160 mg/day of ziprasidone, which reflected the recommended dose range. PET scanning was done after 3 weeks of administration and at trough plasma levels, i.e., 12-16 hours after the last dose.
The mean 5-HT(2) receptor occupancy was significantly higher than the mean D(2) receptor occupancy (mean=76%, SD=15%, and mean=56%, SD=18%, respectively). The estimated plasma ziprasidone concentration associated with 50% maximal 5-HT(2) receptor occupancy was almost four times lower than that for D(2) receptor occupancy.
These data affirm that ziprasidone is similar to other novel antipsychotics in having greater 5-HT(2) than D(2) receptor occupancy at therapeutic doses and suggest that the optimal effective dose of ziprasidone is closer to 120 mg/day than to the lower doses suggested by previous PET studies. The relatively high D(2) receptor occupancy, even at trough plasma levels, suggests that ziprasidone is more similar to risperidone and olanzapine in receptor occupancy profile than to clozapine and quetiapine. Since ziprasidone plasma levels show significant (more than twofold) variation within a single dose cycle, studies that are aimed at peak plasma levels (6 hours after the last dose) and that examine extrastriatal regions are required to fully characterize the in vivo occupancy profile of ziprasidone.
齐拉西酮是一种非典型抗精神病药物,在体外对5-羟色胺5-HT(2)受体的亲和力高于多巴胺D(2)受体。在一项正电子发射断层扫描(PET)研究中检测了齐拉西酮在患者体内对这些受体的亲和力。
作者进行了一项PET研究,以评估16例随机分配接受40、80、120或160mg/日齐拉西酮(反映推荐剂量范围)的精神分裂症或分裂情感性障碍患者感兴趣脑区的D(2)占有率(使用[(11)C]雷氯必利)和5-HT(2)占有率(使用[(18)F]司托哌隆)。给药3周后且在谷血浆水平(即最后一剂后12 - 16小时)时进行PET扫描。
平均5-HT(2)受体占有率显著高于平均D(2)受体占有率(分别为平均 = 76%,标准差 = 15%,以及平均 = 56%,标准差 = 18%)。与50%最大5-HT(2)受体占有率相关的估计血浆齐拉西酮浓度几乎比D(2)受体占有率的浓度低四倍。
这些数据证实,在治疗剂量下,齐拉西酮与其他新型抗精神病药物相似,5-HT(2)受体占有率大于D(2)受体占有率,并表明齐拉西酮的最佳有效剂量更接近120mg/日,而非先前PET研究建议的较低剂量。即使在谷血浆水平时,相对较高的D(2)受体占有率表明,在受体占有率方面,齐拉西酮与利培酮和奥氮平比与氯氮平和喹硫平更相似。由于齐拉西酮血浆水平在单个剂量周期内显示出显著(超过两倍)变化,因此需要针对峰血浆水平(最后一剂后6小时)且检查纹状体以外区域的研究来全面表征齐拉西酮的体内占有率情况。