Positron Medical Center, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
PLoS One. 2011 Mar 9;6(3):e17723. doi: 10.1371/journal.pone.0017723.
The purpose of this study was to determine the binding sites of pramipexole in extrastriatal dopaminergic regions because its antidepressive effects have been speculated to occur by activating the dopamine D(2) receptor subfamily in extrastriatal areas. Dynamic positron emission tomography (PET) scanning using (11)C-FLB 457 for quantification of D(2)/D(3) receptor subtype was performed on 15 healthy volunteers. Each subject underwent two PET scans before and after receiving a single dose of pramipexole (0, 0.125, or 0.25 mg). The study demonstrated that pramipexole significantly binds to D(2)/D(3) receptors in the prefrontal cortex, amygdala, and medial and lateral thalamus at a dose of 0.25 mg. These regions have been indicated to have some relation to depression and may be part of the target sites where pramipexole exerts its antidepressive effects.
这项研究的目的是确定普拉克索在纹状体外多巴胺能区域的结合位点,因为其抗抑郁作用被推测是通过激活纹状体外区域的多巴胺 D2 受体亚家族而产生的。使用 (11)C-FLB 457 进行的动态正电子发射断层扫描 (PET) 扫描用于定量测定 D2/D3 受体亚型,共对 15 名健康志愿者进行了研究。每个受试者在接受普拉克索(0、0.125 或 0.25mg)单剂量之前和之后进行两次 PET 扫描。研究表明,普拉克索在 0.25mg 剂量下可显著结合前额叶皮层、杏仁核以及内侧和外侧丘脑的 D2/D3 受体。这些区域已被表明与抑郁有一定关系,可能是普拉克索发挥抗抑郁作用的靶点部位之一。