Department of Psychiatry, Seoul National University College of Medicine, 28 Yeongon-dong, Chongno-gu, Seoul 110-744, South Korea.
Psychopharmacology (Berl). 2011 Oct;217(4):515-23. doi: 10.1007/s00213-011-2306-4. Epub 2011 Apr 19.
Receptor occupancy study has been performed to evaluate pharmacokinetic profiles in new antipsychotic drug development. While these findings highlight the value of positron emission tomography (PET) for dose-finding study, what is unclear is if it is necessary to conduct these studies in patients with schizophrenia or whether studies in healthy volunteers are adequate.
To determine if it is necessary to conduct dopamine receptor occupancy studies in patients with schizophrenia or whether studies in healthy volunteers are adequate for dose-finding study, we compared the concentration-occupancy relationship in terms of EC(50) between patients and healthy volunteers.
Ten healthy volunteers and eight patients with schizophrenia participated in the study. We measured dopamine receptor occupancy using [(11)C]raclopride PET and plasma concentration of YKP1358, a novel antipsychotic drug under clinical development, at a number of time points after the administration of YKP1358. Pharmacokinetic data including area under the plasma concentration versus time curve, elimination half-life, maximum observed plasma concentration, and the time to reach the maximum observed plasma concentration were obtained. We explored the relationship between plasma concentration and dopamine D(2) receptor occupancy using E (max) model and calculated EC(50).
The elimination half-life was longer in healthy volunteers than in patients. Other pharmacokinetic parameters were not significantly different between two groups. The EC(50) was 7.6 ng/ml (95% confidence interval (CI) 6.2-9.0) in healthy volunteers and 8.6 (95% CI 7.4-9.9) in patients.
The antipsychotic concentration-occupancy relationship in patients can be estimated from the EC(50) data of healthy volunteers.
受体占有率研究已被用于评估新型抗精神病药物开发中的药代动力学特征。虽然这些研究结果强调了正电子发射断层扫描(PET)在剂量发现研究中的价值,但尚不清楚是否有必要在精神分裂症患者中进行这些研究,或者在健康志愿者中进行的研究是否足够。
为了确定是否有必要在精神分裂症患者中进行多巴胺受体占有率研究,或者在健康志愿者中进行的研究是否足以进行剂量发现研究,我们比较了患者和健康志愿者之间 EC(50)的浓度-占有率关系。
10 名健康志愿者和 8 名精神分裂症患者参加了这项研究。我们使用 [(11)C]raclopride PET 测量多巴胺受体占有率,并在 YKP1358 给药后多个时间点测量新型抗精神病药物 YKP1358 的血浆浓度。获得了包括血浆浓度-时间曲线下面积、消除半衰期、最大观测血浆浓度和达到最大观测血浆浓度的时间在内的药代动力学数据。我们使用 E(max)模型探索了血浆浓度与多巴胺 D(2)受体占有率之间的关系,并计算了 EC(50)。
健康志愿者的消除半衰期长于患者。两组间其他药代动力学参数无显著差异。健康志愿者的 EC(50)为 7.6ng/ml(95%置信区间 6.2-9.0),患者为 8.6(95%置信区间 7.4-9.9)。
可以从健康志愿者的 EC(50)数据中估计患者的抗精神病药物浓度-占有率关系。