首页 | 本学科首页   官方微博 | 高级检索  
     


Increased anxiety and "depressive" symptoms months after MDMA ("ecstasy") in rats: drug-induced hyperthermia does not predict long-term outcomes
Authors:Iain?S.?McGregor  author-information"  >  author-information__contact u-icon-before"  >  mailto:iain@psych.usyd.edu.au"   title="  iain@psych.usyd.edu.au"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Clint?G.?Gurtman,Kirsten?C.?Morley,Kelly?J.?Clemens,Arjan?Blokland,Kong?M.?Li,Jennifer?L.?Cornish,Glenn?E.?Hunt
Affiliation:(1) School of Psychology, University of Sydney, Sydney, 2006 NSW, Australia;(2) Department of Psychology, University of Maastricht, Maastricht, The Netherlands;(3) Department of Pharmacology, University of Sydney, Sydney, 2006 NSW, Australia;(4) Department of Psychological Medicine, University of Sydney, Concord Hospital, Sydney, 2139 NSW, Australia
Abstract:Rationale There is some uncertainty whether the acute hyperthermia caused by MDMA (ecstasy) plays a significant role in determining the long-term neurotoxic effects on brain 5-HT systems and associated changes in mood and behaviour. Objective The present study assessed whether long-term behavioural and cognitive changes seen in MDMA-treated rats are affected by hyperthermia at the time of drug administration. Method Male Wistar rats were treated with MDMA (4×5 mg/kg i.p. over 4 h on 2 consecutive days) or vehicle at either a high ambient temperature (28°C) or a low ambient temperature (16°C). Eight to 18 weeks later, rats were tested in behavioural measures of anxiety (social interaction and emergence tests), a test of cognition (object recognition test) and the forced swim test of depression. At the conclusion of behavioural testing the rats were killed and their brains analysed using HPLC. Results MDMA treatment caused a clear and consistent hyperthermia at 28°C and hypothermia at 16°C. Months later, rats pre-treated with MDMA at either 16 or 28°C displayed increased anxiety in the social interaction and emergence tests and reduced escape attempts and increased immobility in the forced swim test. MDMA pre-treatment was also associated with poorer memory on the object recognition test, but only in rats given the drug at 28°C. Rats pre-treated with MDMA showed loss of 5-HT in the hippocampus, striatum, amygdala and cortex, regardless of body temperature at the time of dosing. However, 5-HIAA loss in the amygdala and hippocampus was greater in rats pre-treated at 28°C. Dopamine in the striatum was also depleted in rats given MDMA. Conclusions These results indicate that hyperthermia at the time of dosing with MDMA is not necessary to produce subsequent 5-HT depletion and anxiety in rats. They also extend previous findings of long-term effects of brief exposure to MDMA in rats to include apparent "depressive" symptoms in the forced swim model.
Keywords:MDMA  Ecstasy  Anxiety  Depression  Serotonin  5-HT  Temperature
本文献已被 PubMed SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号