Köhler C, Ogren S O, Haglund L, Angeby T
Neurosci Lett. 1979 Jun;13(1):51-6. doi: 10.1016/0304-3940(79)90074-0.
The regional displacement by sulpiride of [3H]spiperone binding in vivo was studied in the rat. A low dose of sulpiride (20 mg/kg) displaced [3H]spiperone binding in certain limbic regions (olfactory tubercle, septum) and the substantia nigra but not in the nucleus accumbens or striatum. At this does sulpiride preferentially blocked apomorphine induced apomorphine Higher doses of sulpiride (150 and 250 mg/kg), which blocked apomorphine induced stereotypes and induced catalepsy were found to displace [3H]spiperone binding in all regions studied including the striatum and the nucleus accumbens. Haloperidol (0.1 and 1.0 mg/kg) displaced [3H]spiperone to approximately the same extent in all regions studied.
在大鼠体内研究了舒必利对[3H]螺哌隆结合的区域置换作用。低剂量舒必利(20毫克/千克)可置换某些边缘区域(嗅结节、隔区)和黑质中的[3H]螺哌隆结合,但对伏隔核或纹状体无此作用。在此剂量下,舒必利优先阻断阿扑吗啡诱导的刻板行为。高剂量舒必利(150和250毫克/千克)可阻断阿扑吗啡诱导的刻板行为并诱发僵住症,发现其能置换包括纹状体和伏隔核在内的所有研究区域中的[3H]螺哌隆结合。氟哌啶醇(0.1和1.0毫克/千克)在所有研究区域中对[3H]螺哌隆的置换程度大致相同。