Cincotta M, de Vries D J, Beart P M
Neurosci Lett. 1985 Oct 24;61(1-2):85-9. doi: 10.1016/0304-3940(85)90405-7.
The properties of the site labelled by [3H]fluphenazine in membranes prepared from the rat neostriatum were examined using radioligand binding methodology. Binding of [3H]fluphenazine was rapid, saturable and of high affinity (K4 = 0.4 nM). Drug displacement experiments demonstrated that the site labelled by [3H]fluphenazine possessed pharmacological characteristics consistent with those of a D-1 dopamine receptor.
利用放射性配体结合方法,研究了用[³H]氟奋乃静标记的大鼠新纹状体膜位点的特性。[³H]氟奋乃静的结合迅速、可饱和且具有高亲和力(Kd = 0.4 nM)。药物置换实验表明,用[³H]氟奋乃静标记的位点具有与D-1多巴胺受体一致的药理学特性。