Gulat-Marnay C, Lafitte A, Schwartz J C, Protais P
Naunyn Schmiedebergs Arch Pharmacol. 1985 Apr;329(2):117-22. doi: 10.1007/BF00501199.
The in vivo accumulation of 3H-N-propyl norapomorphine in mouse striatum and tuberculum olfactorium and its inhibition by a series of classical neuroleptics and discriminant benzamide derivatives previously identified in behavioural and radioligand experiments has been studied. The ID50 values in the two brain areas did not significantly differ with any studied compound. In addition the regional distribution of a discriminant compound related to sulpiride and administered in tritiated form to rats was rather homogeneous. These data do not indicate a preferential accumulation of these compounds in limbic as opposed to striatal areas.
研究了3H-N-丙基去甲阿朴吗啡在小鼠纹状体和嗅结节中的体内蓄积情况,以及一系列经典抗精神病药物和先前在行为学及放射性配体实验中鉴定出的鉴别性苯甲酰胺衍生物对其的抑制作用。两个脑区中任何所研究化合物的半数抑制浓度(ID50)值均无显著差异。此外,以氚标记形式给予大鼠的一种与舒必利相关的鉴别性化合物在脑中的区域分布相当均匀。这些数据并未表明这些化合物在边缘系统相对于纹状体区域有优先蓄积。