Gramatté T, Wustmann C, Schmidt J, Fischer H D
Biomed Biochim Acta. 1986;45(8):1075-82.
Piracetam (PIR) and dimethylaminoethanol (DMAE) were tested with respect to their ability to prevent changes of the locomotor behaviour and of the dopamine release from striatum slices after an intermittent postnatal hypoxia in the rat (2nd-10th day of postnatal life). The drugs given to pregnant rats (from 12th day of gestation) and continued after delivery to the newborns (till 10th day of postnatal life) displayed antihypoxic effects. Perinatal DMAE- but not PIR-treatment diminishes the consequences of postnatal oxygen deprivation regarding the motor activity as well as the dopamine release of adult animals. Hypoxia-caused open field hyperactivity of developing rats was found to be reduced to control values in PIR-treated rats. Only minor effects were seen after DMAE-treatment, but a marked depressant own effect on the explorative activity was detectable.
在大鼠出生后间歇性缺氧(出生后第2 - 10天)后,对吡拉西坦(PIR)和二甲基乙醇胺(DMAE)预防运动行为变化以及纹状体切片中多巴胺释放变化的能力进行了测试。给怀孕大鼠(从妊娠第12天开始)给药,并在分娩后继续给新生大鼠用药(直至出生后第10天),这些药物显示出抗缺氧作用。围产期使用DMAE而非PIR治疗可减轻出生后缺氧对成年动物运动活动以及多巴胺释放的影响。发现PIR治疗的发育中大鼠因缺氧导致的旷场活动亢进降低至对照值。DMAE治疗后仅观察到轻微影响,但可检测到其对探索活动有明显的自身抑制作用。