Choi S J, Mazzio E, Soliman K F
College of Pharmacy and Pharmaceutical Sciences, Florida A & M University, Tallahassee 32307, USA.
Ann N Y Acad Sci. 1998 May 30;844:324-35.
Pregnant female Sprague-Dawley rats were injected with either 40 mg/kg (-)cocaine hydrochloride or an equivalent volume of 0.9% saline, subcutaneously (s.c.), once daily from gestational day 12 (GD 12) to GD 21. Gestational cocaine exposure had no effect on maternal weight gain, length of gestation, birthweight, fetal mortality, postnatal weight gain or locomotive activity in offspring. There was an unusual reduction in the male/female offspring ratio in the treated group (1:0.65) verses controls (1:1.04) (p < 0.01). Male offspring scored significantly lower on memory and learning tasks on postnatal day 30 (PND30) as determined by the water maze test (p < 0.01). Exposure to cocaine in utero had no effect on postnatal female sexual maturation or cognitive function. The present study indicated that gestational cocaine exposure can lead to cognitive impairment selectively in male offspring, without any apparent postnatal physical abnormalities or adverse effects on maternal health status.
从妊娠第12天(GD 12)至GD 21,每天一次给怀孕的雌性斯普拉格-道利大鼠皮下注射40毫克/千克的(-)盐酸可卡因或等量体积的0.9%生理盐水。孕期接触可卡因对母体体重增加、妊娠期长度、出生体重、胎儿死亡率、产后体重增加或后代的运动活动均无影响。与对照组(1:1.04)相比,治疗组的雄性/雌性后代比例出现异常降低(1:0.65)(p < 0.01)。根据水迷宫试验测定,雄性后代在出生后第30天(PND30)的记忆和学习任务中得分显著较低(p < 0.01)。子宫内接触可卡因对产后雌性性成熟或认知功能没有影响。本研究表明,孕期接触可卡因可选择性地导致雄性后代认知障碍,且产后无明显身体异常或对母体健康状况无不良影响。