Increased anxiety and 'depressive' symptoms months after MDMA ('ecstasy') in rats: drug-induced hyperthermia does not predict long-term outcomes

被引:71
作者
McGregor, IS [1 ]
Gurtman, CG
Morley, KC
Clemens, KJ
Blokland, A
Li, KM
Cornish, JL
Hunt, GE
机构
[1] Univ Sydney, Sch Psychol, Sydney, NSW 2006, Australia
[2] Univ Maastricht, Dept Psychol, Maastricht, Netherlands
[3] Univ Sydney, Dept Psychol, Sydney, NSW 2006, Australia
[4] Univ Sydney, Concord Hosp, Dept Psychol Med, Sydney, NSW 2139, Australia
关键词
MDMA; ecstasy; anxiety; depression; serotonin; 5-HT; temperature;
D O I
10.1007/s00213-003-1452-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 (4x5 mg/kg i.p. over 4 h on 2 consecutive days) or vehicle at either a high ambient temperature (28degreesC) or a low ambient temperature (16degreesC). 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 28degreesC and hypothermia at 16degreesC. Months later, rats pre-treated with MDMA at either 16 or 28degreesC 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 28degreesC. 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 28degreesC. 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.
引用
收藏
页码:465 / 474
页数:10
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