Campbell A, Baldessarini R J, Cremens M C
Department of Psychiatry, Harvard Medical School, Boston, MA 02114.
Neuropharmacology. 1988 Nov;27(11):1197-9. doi: 10.1016/0028-3908(88)90018-4.
Haloperidol induced catalepsy with a continuous dose-response between 0 or 0.03 and 10 mg/kg, IP in Brown Norway (BN), Fischer (FR). Long-Evans (LE), and Sprague-Dawley (SD) rats, with similar ED50 values for males (0.23-0.42 mg/kg), and generally greater but more varied drug sensitivity in females (ED50 = 0.13-0.45 mg/kg). Inconsistent findings regarding a biphasic dose-effect relationship in SD male and LE female rats led to testing both sexes and strains up to 200 mg/kg. Females showed a greater tendency than males of both strains to yield lower catalepsy scores at doses greater than 10 mg/kg, but in association with gross neurological toxicity. This paradigm evidently is not an adequate model for a proposed biphasic relationship between doses of high potency neuroleptic agents and acute dystonia in man.
氟哌啶醇在棕色挪威大鼠(BN)、费希尔大鼠(FR)、长-伊文斯大鼠(LE)和斯普拉格-道利大鼠(SD)中通过腹腔注射连续剂量(0或0.03至10mg/kg)诱发僵住症,雄性大鼠的半数有效剂量(ED50)值相似(0.23 - 0.42mg/kg),而雌性大鼠通常对药物更敏感,但敏感度变化更大(ED50 = 0.13 - 0.45mg/kg)。关于SD雄性大鼠和LE雌性大鼠双相剂量效应关系的研究结果不一致,因此对两种性别和品系的大鼠进行了高达200mg/kg剂量的测试。在剂量大于10mg/kg时,两个品系的雌性大鼠比雄性大鼠更倾向于产生较低的僵住症评分,但这与严重的神经毒性有关。显然,这种范式对于拟议的高效能抗精神病药物剂量与人急性肌张力障碍之间的双相关系而言,并不是一个合适的模型。