Skelton Matthew R, Able Jessica A, Grace Curtis E, Herring Nicole R, Schaefer Tori L, Gudelsky Gary A, Vorhees Charles V, Williams Michael T
Division of Neurology, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, Cincinnati, OH 45229-3039, USA.
Neuropharmacology. 2008 Dec;55(7):1121-30. doi: 10.1016/j.neuropharm.2008.07.006. Epub 2008 Jul 12.
3,4-Methlylenedioxymethamphetamine (MDMA) administration (4 x 15 mg/kg) on a single day has been shown to cause path integration deficits in rats. While most animal experiments focus on single binge-type models of MDMA use, many MDMA users take the drug on a recurring basis. The purpose of this study was to compare the effects of repeated single-day treatments with MDMA (4 x 15 mg/kg) once weekly for 5 weeks to animals that only received MDMA on week 5 and saline on weeks 1-4. In animals treated with MDMA for 5 weeks, there was an increase in time spent in the open area of the elevated zero maze suggesting a decrease in anxiety or increase in impulsivity compared to the animals given MDMA for 1 week and saline treated controls. Regardless of dosing regimen, MDMA treatment produced path integration deficits as evidenced by an increase in latency to find the goal in the Cincinnati water maze. Animals treated with MDMA also showed a transient hypoactivity that was not present when the animals were re-tested at the end of cognitive testing. In addition, both MDMA-treated groups showed comparable hyperactive responses to a later methamphetamine challenge. No differences were observed in spatial learning in the Morris water maze during acquisition or reversal but MDMA-related deficits were seen on reduced platform-size trials. Taken together, the data show that a single-day regimen of MDMA induces deficits similar to that of multiple weekly treatments.
已证实,单日给予大鼠3,4-亚甲基二氧甲基苯丙胺(摇头丸,MDMA,4×15毫克/千克)会导致其路径整合能力缺陷。虽然大多数动物实验聚焦于单次大量使用摇头丸的模型,但许多摇头丸使用者会反复服用该药物。本研究的目的是比较每周一次、连续5周给予大鼠单日剂量的摇头丸(4×15毫克/千克),与仅在第5周给予摇头丸、第1至4周给予生理盐水的动物之间的效果差异。与接受1周摇头丸治疗及生理盐水处理的对照组动物相比,接受5周摇头丸治疗的动物在高架零迷宫开放区域停留的时间增加,这表明其焦虑感降低或冲动性增加。无论给药方案如何,摇头丸治疗均导致路径整合能力缺陷,这在辛辛那提水迷宫中寻找目标的潜伏期增加上得到了证明。接受摇头丸治疗的动物还表现出短暂的活动减少,但在认知测试结束时再次测试时未出现这种情况。此外,两个接受摇头丸治疗的组对随后的甲基苯丙胺激发均表现出类似的多动反应。在莫里斯水迷宫的获取或反转过程中,未观察到空间学习方面的差异,但在平台尺寸减小的试验中发现了与摇头丸相关的缺陷。综上所述,数据表明,单日剂量的摇头丸诱导的缺陷与每周多次治疗相似。