Lyon M, McClure W O
Center for Brain and Behavior Study, University of Arkansas for Medical Sciences, Little Rock.
Psychopharmacology (Berl). 1994 Oct;116(2):226-36. doi: 10.1007/BF02245066.
Recent evidence suggests that mid-pregnancy is a critical period for production of fetal abnormalities that cause behavioral and neuropathological changes in adult offspring. The present experiments provide an animal model of these effects by treating pregnant Sprague-Dawley rats during gestational days 11-14 with d-amphetamine (AM). Offspring were tested for neurological signs, foraging activity, reversal learning, and sensitivity to amphetamine challenge. In the Early Juvenile period, postnatal days (PND) 20-30, female AM offspring initially showed reductions in rearing, holepoking, and midfield activity. On later trials, and as young adults, AM females showed signs of locomotor hyperactivity despite continued poor foraging efficiency, and were also more sensitive to a 1.0 mg/kg d-amphetamine challenge. AM males showed initially slower and more perseverative responding than controls, but then developed excessive response switching. These changes continued during tests for Retention, Reversal, and Extinction in the Late Juvenile/Early Adult stage (PND 50-90), when both AM-exposed sexes showed increased eating time, significantly more perseverative lateral turning preference (right or left), and slower reversal learning than controls. Behavioral data were consistent with aberrations in thalamo-frontal and mesolimbic/nigrostriatal projection systems that have been reported in AM animals and which are also affected by maternal drug abuse and schizophrenia.
最近的证据表明,孕中期是胎儿产生异常的关键时期,这些异常会导致成年后代出现行为和神经病理学变化。本实验通过在妊娠第11 - 14天用右旋苯丙胺(AM)处理怀孕的斯普拉格-道利大鼠,提供了这些影响的动物模型。对后代进行神经体征、觅食活动、逆向学习以及对苯丙胺激发的敏感性测试。在幼年期早期,即出生后第20 - 30天,雌性AM后代最初表现出竖毛、探洞和中场活动减少。在随后的试验中,以及成年后,AM雌性尽管觅食效率持续低下,但仍表现出运动亢进的迹象,并且对1.0 mg/kg的右旋苯丙胺激发也更敏感。AM雄性最初比对照组反应更慢且更具持续性,但随后出现过度的反应转换。在幼年期晚期/成年早期阶段(出生后第50 - 90天)进行的保持、逆向和消退测试中,这些变化持续存在,此时暴露于AM的两性都表现出进食时间增加、明显更多的持续性侧转偏好(向右或向左),并且逆向学习比对照组更慢。行为数据与AM动物中报道的丘脑-额叶和中脑边缘/黑质纹状体投射系统的畸变一致,这些系统也受到母体药物滥用和精神分裂症的影响。