Hrebíčková I, Malinová-Ševčíková M, Macúchová E, Nohejlová K, Šlamberová R
Department of Normal, Pathological and Clinical Physiology, Third Faculty of Medicine, Prague, Czech Republic.
Physiol Res. 2014;63(Suppl 4):S535-45. doi: 10.33549/physiolres.932927.
It is known that psychostimulants including methamphetamine (MA) have neurotoxic effect, especially, if they are targeting CNS during its critical periods of development. The present study was aimed on evaluation of cognitive changes following scheduled prenatal MA exposure in combination with long-term exposure in adulthood of male rats. Two periods of gestation were targeted: 1(st) half - the embryonic day (ED) 1-11 and 2(nd) half - ED 12-22. Rat mothers received subcutaneously a daily injection of MA (5 mg/kg) or saline (SAL, 1 ml/kg) throughout scheduled periods. Male offspring were tested for cognitive changes in the Morris Water Maze (MWM) in adulthood. Each day of the experiment animals received an injection of MA (1 mg/kg) or SAL (1 ml/kg) during 12 days. Our results demonstrated that in the group of animals exposed to the drug during ED 1-11, neither prenatal MA exposure, nor adult MA treatment changed the performance in the MWM test. Only the velocity was increased in group with long-term MA treatment (SAL/MA and MA/MA). In the group of animals exposed to the drug during ED 12-22, rats exposed to MA prenatally and also in adulthood (MA/MA) swam faster but learned the position of the platform slower in the Place Navigation Test than animals exposed to SAL in adulthood (MA/SAL). In the Probe Test, MA/SAL had decreased velocity and swam shorter distance than MA/MA or SAL/SAL rats suggesting increased floating of these animals. In the Memory Retention Test, SAL/MA rats swam shorter distance than SAL/SAL or MA/MA animals suggesting changes in used strategies in memory recall. As conclusion, our results suggest differences in the effect of combination of prenatal and adult exposure to MA. These effects further depend on the stage of CNS development and schedule of MA exposure affecting intrauterine development in male rats.
众所周知,包括甲基苯丙胺(MA)在内的精神兴奋剂具有神经毒性作用,尤其是在中枢神经系统发育的关键时期作用于中枢神经系统时。本研究旨在评估雄性大鼠在孕期按计划接触MA并在成年期长期接触后的认知变化。研究针对两个妊娠期:第一个半期——胚胎期第1至11天,第二个半期——胚胎期第12至22天。在预定时间段内,大鼠母亲每天皮下注射MA(5毫克/千克)或生理盐水(SAL,1毫升/千克)。成年雄性后代在莫里斯水迷宫(MWM)中接受认知变化测试。在实验的每一天,动物在12天内接受MA(1毫克/千克)或SAL(1毫升/千克)注射。我们的结果表明,在胚胎期第1至11天接触药物的动物组中,孕期MA暴露和成年期MA治疗均未改变MWM测试中的表现。只有长期接受MA治疗的组(SAL/MA和MA/MA)速度有所增加。在胚胎期第12至22天接触药物的动物组中,孕期和成年期均接触MA的大鼠(MA/MA)在位置导航测试中游泳速度更快,但学习平台位置的速度比成年期接触SAL的大鼠(MA/SAL)慢。在探针测试中,MA/SAL的速度降低,游泳距离比MA/MA或SAL/SAL大鼠短,表明这些动物漂浮增加。在记忆保持测试中,SAL/MA大鼠游泳的距离比SAL/SAL或MA/MA动物短,表明记忆回忆中使用的策略发生了变化。总之,我们的结果表明孕期和成年期接触MA的联合效应存在差异。这些效应进一步取决于中枢神经系统发育阶段和MA暴露时间表,从而影响雄性大鼠的子宫内发育。