Department of Pharmacology, Toxicology and Neuroscience, LSU Health Sciences Center - Shreveport, Shreveport, LA 71130-3932, USA.
Behav Brain Res. 2010 Sep 1;212(1):27-34. doi: 10.1016/j.bbr.2010.03.022. Epub 2010 Mar 20.
Recent changes in demographic patterns of drug use have resulted in the increased non-medical use of prescription opiates. These users are younger and more likely to be female, which has the potential for increasing rates of in utero exposure. Therefore, we developed a rat model that simulates a prescription opiate-dependent woman who becomes pregnant. Adult female Sprague-Dawley rats were treated for 30 days via oral gavage with ascending doses of oxycodone HCl up to a final dose of 15mg/kg/day, which was maintained during breeding and gestation. Controls were treated with water. The adult male offspring of these treated dams were tested on the radial arm maze, the Morris water maze (with a short and a long intertrial interval), and a spatial T-maze. Prenatal oxycodone exposure led to a deficit in the radial arm maze characterized by a greater number of reference memory errors, especially in the beginning of testing. In contrast, in the T-maze, prenatal oxycodone-exposed rats learned the task as well as well as the prenatal water controls. However, they had a modest deficit in retention of the task when assessed 5 days after acquisition training ended. For the Morris water maze, the intertrial interval affected the pattern of learning. While there was no deficit when the training had a short intertrial interval, when there was a long intertrial interval, prenatal oxycodone-exposed rats had poorer acquisition. The spatial learning deficit was characterized by and increased latency to find and a greater distance traveled to the platform in the prenatal oxycodone-exposed rats. These data were corroborated by analysis of the behavioral search strategy, which showed a decreased use of spatial strategies and an increase in non-spatial strategies, especially wall-hugging, in prenatal oxycodone-exposed rats as compared to prenatal water control rats on day 2 of acquisition. These results indicate that prenatal oxycodone exposure consistently impairs learning and memory in a battery of spatial tasks.
最近药物使用的人口统计学模式发生了变化,导致非医疗用途的处方阿片类药物增加。这些使用者更年轻,更有可能是女性,这有可能增加胎儿暴露的风险。因此,我们建立了一个模拟依赖处方阿片类药物的怀孕女性的大鼠模型。成年雌性 Sprague-Dawley 大鼠通过口服灌胃接受 30 天递增剂量的盐酸羟考酮,最高剂量为 15mg/kg/天,在繁殖和妊娠期间维持该剂量。对照组给予水。这些处理后的母鼠的成年雄性后代在放射臂迷宫、莫里斯水迷宫(短和长的间隔时间)和空间 T 迷宫上进行测试。产前羟考酮暴露导致在放射臂迷宫中出现参考记忆错误的数量增加,特别是在测试开始时,表现出缺陷。相比之下,在 T 迷宫中,产前羟考酮暴露的大鼠与产前水对照组一样学习任务。然而,在获得训练结束后 5 天进行评估时,它们在保留任务方面存在适度的缺陷。对于 Morris 水迷宫,试验间隔时间影响学习模式。当训练间隔时间较短时,没有缺陷,而当训练间隔时间较长时,产前羟考酮暴露的大鼠则获得能力较差。空间学习缺陷的特征是潜伏期增加,找到平台的距离增加,产前羟考酮暴露的大鼠的距离增加。这些数据通过分析行为搜索策略得到证实,该策略显示产前羟考酮暴露的大鼠在获得训练的第 2 天比产前水对照组大鼠减少了空间策略的使用,并增加了非空间策略的使用,尤其是壁式抱。这些结果表明,产前羟考酮暴露一致地损害了一系列空间任务中的学习和记忆能力。