Ludwig V, Mihov Y, Schwarting R K W
Experimental and Physiological Psychology, Philipps-University of Marburg, Gutenbergstr. 18, 35037 Marburg, Germany.
Behav Brain Res. 2008 May 16;189(1):52-64. doi: 10.1016/j.bbr.2007.12.008. Epub 2007 Dec 23.
Using the elevated plus-maze (EPM), Wistar rats can be distinguished into high (HA) or low anxiety (LA) subjects. These differences seem to reflect traits, since HA and LA rats vary also in other anxiety-dependent tasks, neurochemical mechanisms, and psychopharmacological reactivity, including lasting consequences after single treatment with 3,4-methylenedioxymethamphetamine (MDMA). Here, we tested whether multiple MDMA treatments also have subject-dependent effects. Based on routine EPM screening, male Wistar rats were divided into HA and LA sub-groups, which received five (i.e. multiple) daily injections of MDMA (5 mg/kg) or saline, followed by a test battery, including a challenge test with MDMA, a retest in the EPM, a novel-object test, and a final neurochemical analysis. Acutely, MDMA led to comparable hyperactivity in HA and LA rats. After multiple MDMA, behavioral sensitization was observed, especially in LA rats. Open arm time during the EPM retest (min 0-5) correlated with that of the initial one only in those rats, which had received a single injection of MDMA. Rats with multiple MDMA, especially LA-rats, showed more open-arm time and locomotion during the subsequent 5-10 min of the retest. In a novel-object test, rats with multiple MDMA, again especially LA subjects, showed more exploratory bouts towards the novel object. Neurochemically, multiple MDMA led to moderately lower serotonin in the ventral striatum, and higher dopamine levels in the frontal cortex as compared to single MDMA; these effects were also moderated by subject-dependent factors. Our data show that low-dosed multiple MDMA can lead to behavioral sensitization and outlasting consequences, which affect behavior in the EPM and a novel object task. Detecting such sequels partly requires consideration of individual differences.
使用高架十字迷宫(EPM),可以将Wistar大鼠区分为高焦虑(HA)或低焦虑(LA)个体。这些差异似乎反映了特质,因为HA和LA大鼠在其他依赖焦虑的任务、神经化学机制以及精神药理反应性方面也存在差异,包括单次使用3,4-亚甲基二氧甲基苯丙胺(MDMA)治疗后的长期后果。在此,我们测试了多次MDMA治疗是否也有个体依赖性效应。基于常规的EPM筛选,将雄性Wistar大鼠分为HA和LA亚组,分别每日接受五次(即多次)MDMA(5mg/kg)或生理盐水注射,随后进行一系列测试,包括MDMA激发试验、EPM重测、新物体试验以及最终的神经化学分析。急性给药时,MDMA在HA和LA大鼠中引起了相当的多动。多次给予MDMA后,观察到行为敏化现象,尤其是在LA大鼠中。只有在那些接受过单次MDMA注射的大鼠中,EPM重测(0-5分钟)期间的开臂时间才与初始时相关。多次接受MDMA治疗的大鼠,尤其是LA大鼠,在重测的后续5-10分钟内表现出更多的开臂时间和活动。在新物体试验中,多次接受MDMA治疗的大鼠,同样尤其是LA个体,对新物体表现出更多的探索行为。神经化学方面,与单次MDMA相比,多次MDMA导致腹侧纹状体中的5-羟色胺略有降低,额叶皮质中的多巴胺水平升高;这些效应也受到个体依赖性因素的调节。我们的数据表明,低剂量多次MDMA可导致行为敏化和持久后果,影响EPM和新物体任务中的行为。检测此类后遗症部分需要考虑个体差异。