Relevance of MDMA ("ecstasy")-induced neurotoxicity to long-lasting psychomotor stimulation in mice

被引:42
|
作者
Itzhak, Y
Ali, SF
Achat, CN
Anderson, KL
机构
[1] Univ Miami, Sch Med, Dept Psychiat & Behav Sci R629, Miami, FL 33136 USA
[2] US FDA, Natl Ctr Toxicol Res, Div Neurotoxicol, Jefferson, AR 72079 USA
关键词
MDMA; cocaine; neurotoxicity; sensitization; hyperlocomotion;
D O I
10.1007/S00213-002-1320-y
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Although many studies have focused on the mechanisms underlying MDMA-induced neurotoxicity, little is known about the subsequent longterm response to psychostimulants following exposure to a neurotoxic dose of MDMA. Objectives: We investigated the effect of pre-exposure to neurotoxic and non-neurotoxic doses of MDMA on the response of mice to the psychomotor stimulating effects of MDMA and cocaine. Methods: To investigate MDMA-induced neurotoxicity, male Swiss Webster mice were subjected to three regimens of MDMA: i) 40 mg/kgx2, ii) 30 mg/kgx2, and iii) 15 mg/kgx2 for 2 days. On day 5 following the last exposure to MDMA, the levels of dopaminergic and serotonergic markers were determined. For the behavioral experiments, mice received either a single injection of 10 mg/kg MDMA [MDMA(L)] or one of the following doses of MDMA: 30 mg/kgx2 or 15 mg/kgx2 for 2 days [MDMA (H)]. A third group received saline as a control. On day 5 after the last pretreatment injection, the first MDMA (10 mg/kg) challenge was given, and on day 12, cocaine (20 mg/kg) was administered. Subsequently, mice were re-challenged with MDMA on days 35, 50 and 80, after which locomotor activity was monitored by infrared beam-interrupts. On day 83, mice were killed to detect the levels of doparninergic and serotonergic markers. Results: MDMA-induced mortality and depletion of dopaminergic and serotonergic markers were dose-dependent. MDMA (H) mice endured a sensitized response to MDMA challenge from days 5 through 80, e.g. a persistent 3-fold increase in locomotor activity compared to the response of mice that were not pretreated with a neurotoxic dose of MDMA. The depletion of DAT and 5-HTT binding sites was sustained throughout this time period (64-68% of control). The MDMA (L) mice showed a sensitized response to MDMA only on day 5. Both MDMA (L) and MDMA (H) mice were sensitized to the cocaine challenge. Conclusions: The induction of sensitization to the locomotor stimulating effects of MDMA and cocaine was independent of MDMA-induced neurotoxicity. However, the long-lasting maintenance of the sensitized response to MDMA may be related to the enduring neurotoxicity caused by MDMA.
引用
收藏
页码:241 / 248
页数:8
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