Kutlu Munir Gunes, Braak David C, Tumolo Jessica M, Gould Thomas J
Department of Psychology, Neuroscience Program, Weiss Hall, Temple University, 1701 N. 13th St, Philadelphia, PA 19122, USA.
Department of Psychology, Neuroscience Program, Weiss Hall, Temple University, 1701 N. 13th St, Philadelphia, PA 19122, USA.
Brain Res. 2016 Jul 1;1642:445-451. doi: 10.1016/j.brainres.2016.04.023. Epub 2016 Apr 13.
Adolescence is a critical developmental period associated with both increased vulnerability to substance abuse and maturation of certain brain regions important for learning and memory such as the hippocampus. In this study, we employed a hippocampus-dependent learning context pre-exposure facilitation effect (CPFE) paradigm in order to test the effects of acute nicotine on contextual processing during adolescence (post-natal day (PND) 38) and adulthood (PND 53). In Experiment 1, adolescent or adult C57BL6/J mice received either saline or one of three nicotine doses (0.09, 0.18, and 0.36mg/kg) prior to contextual pre-exposure and testing. Our results demonstrated that both adolescent and adult mice showed CPFE in the saline groups. However, adolescent mice only showed acute nicotine enhancement of CPFE with the highest nicotine dose whereas adult mice showed the enhancing effects of acute nicotine with all three doses. In Experiment 2, to determine if the lack of nicotine's effects on CPFE shown by adolescent mice is specific to the age when they are tested, mice were either given contextual pre-exposure during adolescence or adulthood and received immediate shock and testing during adulthood after a 15day delay. We found that both adolescent and adult mice showed CPFE in the saline groups when tested during adulthood. However, like Experiment 1, mice that received contextual pre-exposure during adolescence did not show acute nicotine enhancement except at the highest dose (0.36mg/kg) whereas both low (0.09mg/kg) and high (0.36mg/kg) doses enhanced CPFE in adult mice. Finally, we showed that the enhanced freezing response found with 0.36mg/kg nicotine in the 15-day experiment may be a result of decreased locomotor activity as mice that received this dose of nicotine traveled shorter distances in an open field paradigm. Overall, our results indicate that while adolescent mice showed normal contextual processing when tested both during adolescence and adulthood, they are less sensitive to the enhancing effects of nicotine on contextual processing.
青春期是一个关键的发育时期,在此期间,个体对药物滥用的易感性增加,同时某些对学习和记忆很重要的脑区(如海马体)也在成熟。在本研究中,我们采用了一种依赖海马体的学习情境预暴露促进效应(CPFE)范式,以测试急性尼古丁对青春期(出生后第38天)和成年期(出生后第53天)情境处理的影响。在实验1中,青春期或成年C57BL6/J小鼠在情境预暴露和测试前接受生理盐水或三种尼古丁剂量之一(0.09、0.18和0.36mg/kg)。我们的结果表明,生理盐水组的青春期和成年小鼠均表现出CPFE。然而,青春期小鼠仅在最高尼古丁剂量时表现出急性尼古丁增强CPFE,而成年小鼠在所有三种剂量时均表现出急性尼古丁的增强作用。在实验2中,为了确定青春期小鼠对CPFE缺乏尼古丁效应是否特定于测试时的年龄,小鼠在青春期或成年期接受情境预暴露,并在延迟15天后成年期接受即时电击和测试。我们发现,成年期测试时,生理盐水组的青春期和成年小鼠均表现出CPFE。然而,与实验1一样,青春期接受情境预暴露的小鼠除最高剂量(0.36mg/kg)外未表现出急性尼古丁增强作用,而低剂量(0.09mg/kg)和高剂量(0.36mg/kg)均增强了成年小鼠的CPFE。最后,我们表明,在15天实验中用0.36mg/kg尼古丁发现的增强的僵住反应可能是运动活动减少的结果,因为接受该剂量尼古丁的小鼠在旷场范式中移动的距离较短。总体而言,我们的结果表明,虽然青春期小鼠在青春期和成年期测试时均表现出正常的情境处理,但它们对尼古丁对情境处理的增强作用较不敏感。