Arakawa Ryosuke, Ito Hiroshi, Takano Akihiro, Takahashi Hidehiko, Morimoto Takuya, Sassa Takeshi, Ohta Katsuya, Kato Motoichiro, Okubo Yoshiro, Suhara Tetsuya
Department of Molecular Neuroimaging, Molecular Imaging Center, National Institute of Radiological Sciences, 4-9-1, Anagawa, Inage-ku, Chiba 263-8555, Japan.
Psychopharmacology (Berl). 2008 Apr;197(2):229-35. doi: 10.1007/s00213-007-1029-z. Epub 2007 Dec 6.
Paliperidone ER is a novel antipsychotic drug in an extended-release (ER) formulation. As with all antipsychotics, careful dose setting is necessary to avoid side effects.
In this study, we measured striatal and extrastriatal dopamine D2 receptor occupancy during paliperidone ER treatment in patients with schizophrenia using positron emission tomography (PET) to compare regional occupancy and to estimate the optimal dose.
Thirteen male patients with schizophrenia participated in this 6-week multiple-dose study. Six of them took 3 mg of paliperidone ER per day, four took 9 mg, and three took 15 mg. Two to 6 weeks after first drug intake, two PET scans, one with [11C]raclopride and one with [11C]FLB 457, were performed in each patient on the same day. The relationship between the dose or plasma concentration of paliperidone and dopamine D2 receptor occupancy was calculated.
The dopamine D2 receptor occupancies in the striatum measured with [11C]raclopride and the temporal cortex measured with [11C]FLB 457 were 54.2-85.5% and 34.5-87.3%, respectively. ED50 values of the striatum and temporal cortex were 2.38 and 2.84 mg/day, respectively. There was no significant difference in dopamine D2 receptor occupancy between the striatum and the temporal cortex.
The data from this study suggest that paliperidone ER at 6-9 mg provides an estimated level of dopamine D2 receptor occupancy between 70-80% and that the magnitude of dopamine D2 receptor occupancy is similar between the striatum and temporal cortex.
帕利哌酮缓释片是一种新型的缓释型抗精神病药物。与所有抗精神病药物一样,需要谨慎设定剂量以避免副作用。
在本研究中,我们使用正电子发射断层扫描(PET)测量了精神分裂症患者接受帕利哌酮缓释片治疗期间纹状体和纹状体以外区域的多巴胺D2受体占有率,以比较区域占有率并估计最佳剂量。
13名男性精神分裂症患者参与了这项为期6周的多剂量研究。其中6人每天服用3毫克帕利哌酮缓释片,4人服用9毫克,3人服用15毫克。在首次服药后2至6周,每位患者在同一天进行两次PET扫描,一次使用[11C]雷氯必利,一次使用[11C]FLB 457。计算帕利哌酮的剂量或血浆浓度与多巴胺D2受体占有率之间的关系。
用[11C]雷氯必利测量的纹状体中多巴胺D2受体占有率和用[11C]FLB 457测量的颞叶皮质中多巴胺D2受体占有率分别为54.2 - 85.5%和34.5 - 87.3%。纹状体和颞叶皮质的半数有效剂量(ED50)值分别为2.38和2.84毫克/天。纹状体和颞叶皮质之间的多巴胺D2受体占有率没有显著差异。
本研究数据表明,6 - 9毫克的帕利哌酮缓释片可使多巴胺D2受体占有率估计在70 - 80%之间,且纹状体和颞叶皮质之间的多巴胺D2受体占有率幅度相似。