A review of the mechanisms involved in the acute MDMA (ecstasy)-induced hyperthermic response

被引:119
作者
Green, AR
O'Shea, E
Colado, MI
机构
[1] AstraZeneca R&D Charnwood, Loughborough LE11 5RH, Leics, England
[2] De Montfort Univ, Sch Pharm, Neuropharmacol Res Grp, Leicester LE1 9BH, Leics, England
[3] Univ Complutense Madrid, Fac Med, Dept Farmacol, E-28040 Madrid, Spain
关键词
3,4-methylenedioxymethamphetamine; ecstasy; hyperthermia; neurotoxicity; serotonin; body temperature;
D O I
10.1016/j.ejphar.2004.07.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The predominant severe acute adverse effect following ingestion of 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) by recreational users is hyperthermia which can induce other associated clinical problems and occasionally death. There is no pharmacologically specific treatment. MDMA also induces dose-dependent hyperthermia in experimental animals. This review examines the consequences of MDMA administration on body temperature in humans and rodents. In rats hyperthermia results primarily from dopamine release and is influenced by dose, ambient temperature and other housing conditions. The response is increased in rats with a prior MDMA-induced neurotoxic lesion of 5-hydroxytryptamine (5-HT) nerve endings. Increased MDMA-induced locomotor activity appears to play no role in the hyperthermic response. However, the size of the acute hyperthermic response plays a major role in determining the severity of the subsequent neurotoxicity. These results suggest that any MDMA-induced hyperthermic response will be enhanced in hot, crowded dance club conditions and that ingesting the drug in such conditions increases the possibility of subsequent cerebral neurotoxic effect. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:3 / 13
页数:11
相关论文
共 78 条
[1]   AMPHETAMINE TOXICITY IN AGGREGATED MICE [J].
ASKEW, BM .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1961, 13 (11) :701-&
[2]   ECSTASY AND DANTROLENE [J].
BARRETT, PJ .
BRITISH MEDICAL JOURNAL, 1992, 305 (6863) :1225-1225
[3]   THE SUBSTITUTED AMPHETAMINES 3,4-METHYLENEDIOXYMETHAMPHETAMINE, METHAMPHETAMINE, PARA-CHLOROAMPHETAMINE AND FENFLURAMINE INDUCE 5-HYDROXYTRYPTAMINE RELEASE VIA A COMMON MECHANISM BLOCKED BY FLUOXETINE AND COCAINE [J].
BERGER, UV ;
GU, XF ;
AZMITIA, EC .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 215 (2-3) :153-160
[4]   Effect of 5-HT depletion by MDMA on hyperthermia and Arc mRNA induction in rat brain [J].
Beveridge, TJR ;
Mechan, AO ;
Sprakes, M ;
Pei, Q ;
Zetterstrom, TSC ;
Green, AR ;
Elliott, JM .
PSYCHOPHARMACOLOGY, 2004, 173 (3-4) :346-352
[5]  
BROENING HW, 1995, J PHARMACOL EXP THER, V275, P325
[6]   Brain sites of action of endogenous interleukin-1 in the febrile response to localized inflammation in the rat [J].
Cartmell, T ;
Luheshi, GN ;
Rothwell, NJ .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 518 (02) :585-594
[7]   Effect of 3,4-methylenedioxymethampheta mine ("ecstasy") on body temperature and liver antioxidant status in mice: influence of ambient temperature [J].
Carvalho, M ;
Carvalho, F ;
Remiao, F ;
Pereira, MD ;
Pires-das-Neves, R ;
Bastos, MD .
ARCHIVES OF TOXICOLOGY, 2002, 76 (03) :166-172
[8]  
CHANCE MRA, 1946, J PHARMACOL EXP THER, V87, P214
[9]   Role of hyperthermia in the protective action of clomethiazole against MDMA ('ecstasy')-induced neurodegeneration, comparison with the novel NMDA channel blocker AR-R15896AR [J].
Colado, MI ;
Granados, R ;
O'Shea, E ;
Esteban, B ;
Green, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 124 (03) :479-484
[10]   Studies on the role of dopamine in the degeneration of 5-HT nerve endings in the brain of Dark Agouti rats following 3,4-methylenedioxymethamphetamine (MDMA or 'ecstasy') administration [J].
Colado, MI ;
O'Shea, E ;
Granados, R ;
Esteban, B ;
Martín, AB ;
Green, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 126 (04) :911-924