Schmidt M H, Lee T
Faculty of Medicine, University of Toronto, Ont., Canada.
Psychiatry Res. 1991 Mar;36(3):319-28. doi: 10.1016/0165-1781(91)90030-s.
To test the hypothesis that neuroleptic blockade impairs the development of striatal dopamine D2 receptors, pregnant rats were given haloperidol, thiothixene, or trifluoperazine for gestational days 15-18 (short-term exposure) or days 5-20 (long-term exposure). All of the drugs were demonstrated to cross the placenta and enter the fetal brains equally well. Striatal dopamine D2 receptors of the pups were assayed on postnatal day 14. Neither receptor density nor receptor affinity was altered significantly by the short- or long-term prenatal neuroleptic treatment.
为了验证抗精神病药物阻断会损害纹状体多巴胺D2受体发育这一假说,给怀孕大鼠在妊娠第15 - 18天(短期暴露)或第5 - 20天(长期暴露)给予氟哌啶醇、替沃噻吨或三氟拉嗪。所有药物均被证明能穿过胎盘并同样良好地进入胎儿大脑。在出生后第14天对幼崽的纹状体多巴胺D2受体进行检测。产前短期或长期使用抗精神病药物治疗均未显著改变受体密度或受体亲和力。