Takano Akihiro, Suhara Tetsuya, Ichimiya Tetsuya, Yasuno Fumihiko, Suzuki Kazutoshi
Brain Imaging Project, National Institute of Radiological Sciences, Chiba, Japan.
J Clin Psychopharmacol. 2006 Apr;26(2):188-91. doi: 10.1097/01.jcp.0000203201.34323.d3.
The pharmacokinetics of drugs with specific binding sites in the brain needs to be evaluated at these sites. In this study, we measured the time course of the selective serotonin reuptake inhibitor fluvoxamine in the human brain based on serotonin transporter (5-HTT) occupancy by positron emission tomography. Consecutive positron emission tomography scans were performed using [11C]3-amino-4-(2-dimethylaminomethyl-phenylsulfanyl)-benzonitrile before, 5 hours, 26 hours, and 53 hours after 50 mg of fluvoxamine administration in 6 healthy male volunteers (mean, 24.3 +/- 4.8 years). Quantification was performed using the multilinear reference tissue model 2. Mean 5-HTT occupancies were 72.9% +/- 4.9% at 5 hours, 50.3% +/- 11.0% at 26 hours, and 24.7% +/- 15.3% at 53 hours, and plasma concentrations were 13.9 +/- 5.5 ng/mL at 5 hours, 5.1 +/- 3.2 ng/mL at 26 hours, and 1.5 +/- 1.7 ng/mL at 53 hours. The relationship between the plasma concentration of fluvoxamine and 5-HTT occupancy at these different time points was fitted to the law of mass action.
在大脑中具有特定结合位点的药物的药代动力学需要在这些位点进行评估。在本研究中,我们基于正电子发射断层扫描对血清素转运蛋白(5-HTT)的占据情况,测量了选择性5-羟色胺再摄取抑制剂氟伏沙明在人脑中的时间进程。在6名健康男性志愿者(平均年龄24.3±4.8岁)中,于服用50 mg氟伏沙明前、服用后5小时、26小时和53小时,使用[11C]3-氨基-4-(2-二甲基氨基甲基-苯基硫烷基)-苄腈进行连续的正电子发射断层扫描。使用多线性参考组织模型2进行定量分析。5小时时平均5-HTT占据率为72.9%±4.9%,26小时时为50.3%±11.0%,53小时时为24.7%±15.3%,血浆浓度在5小时时为13.9±5.5 ng/mL,26小时时为5.1±3.2 ng/mL,53小时时为1.5±1.7 ng/mL。氟伏沙明血浆浓度与这些不同时间点的5-HTT占据率之间的关系符合质量作用定律。