Effect of GBR 12909 and fluoxetine on the acute and long term changes induced by MDMA ('ecstasy') on the 5-HT and dopamine concentrations in mouse brain

被引:85
作者
O'Shea, E
Esteban, B
Camarero, J
Green, AR
Colado, MI [1 ]
机构
[1] Univ Complutense Madrid, Fac Med, Dept Farmacol, Madrid 28040, Spain
[2] De Montfort Univ, Sch Pharm & Pharmaceut Sci, Leicester LE1 9RH, Leics, England
关键词
3,4-methylenedioxymethamphetamine; MDMA; ecstasy; GBR; 12909; fluoxetine; dopamine; 5-hydroxytryptamine; neuroprotection; hyperthermia;
D O I
10.1016/S0028-3908(00)00106-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We examined the long term effect of 3,4 methylenedioxymethamphetamine (MDMA, 10, 20 and 30 mg/kg, i.p.) on the cerebral 5-hydroxytryptamine (5-HT) and dopamine content in Swiss Webster mice. Three injections of MDMA (20 or 30 mg/kg, i.p.) given 3 h apart produced a marked depletion in the striatal content of dopamine and its metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) 7 days later. None of the doses administered altered the concentration of 5-HT or its metabolite 5-hydroxyindoleacetic acid (5-HIAA) in several brain areas. Pre-treatment with the dopamine uptake inhibitor GBR 12909 (10 mg/kg, i.p.), 30 min before each of the three MDMA (30 mg/kg, i.p.) injections, completely prevented the long term loss in the striatal catechol concentrations. However, GBR 12909 (10 mg/kg, i.p.) not only failed to prevent the acute effects induced by MDMA (30 mg/kg x 3, i.p.) on dopamine metabolism 30 min later, but in fact potentiated them. The 5-HT uptake inhibitor, fluoxetine (10 mg/kg, i.p.) failed to prevent both the acute and long term dopaminergic deficits. MDMA (30 mg/kg x 3) altered the body temperature of the mice biphasically, producing a rapid hyperthermia followed by prolonged hypothermia. In contrast, MDMA (20 mg/kg x 3) produced an initial hypothermia followed by hyperthermia. The present experiments therefore appear to rule out any direct relationship between the neurotoxic effects of MDMA and its acute effects on body temperature in mice. Fluoxetine administered 30 min before each MDMA (30 mg/kg) injection prevented these temperature changes, while GBR 12909 was without effect. This suggests that the neuroprotective effect of GBR 12909 against MDMA-induced neurotoxicity is not directly related to its ability to inhibit the MDMA-induced acute effects on dopamine metabolism or alter the MDMA-induced temperature change. The data illustrate major differences in the neurotoxic profile of MDMA in mice and rats. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:65 / 74
页数:10
相关论文
共 55 条
[2]   STRIATAL DOPAMINE RELEASE INVIVO FOLLOWING NEUROTOXIC DOSES OF METHAMPHETAMINE AND EFFECT OF THE NEUROPROTECTIVE DRUGS, CHLORMETHIAZOLE AND DIZOCILPINE [J].
BALDWIN, HA ;
COLADO, MI ;
MURRAY, TK ;
DESOUZA, RJ ;
GREEN, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :590-596
[3]   MDMA-INDUCED NEUROTOXICITY - PARAMETERS OF DEGENERATION AND RECOVERY OF BRAIN-SEROTONIN NEURONS [J].
BATTAGLIA, G ;
YEH, SY ;
DESOUZA, EB .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1988, 29 (02) :269-274
[4]  
BATTAGLIA G, 1987, J PHARMACOL EXP THER, V242, P911
[5]   EFFECTS OF A COLD ENVIRONMENT OR AGE ON METHAMPHETAMINE-INDUCED DOPAMINE RELEASE IN THE CAUDATE PUTAMEN OF FEMALE RATS [J].
BOWYER, JF ;
GOUGH, B ;
SLIKKER, W ;
LIPE, GW ;
NEWPORT, GD ;
HOLSON, RR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1993, 44 (01) :87-98
[6]  
BOWYER JF, 1994, J PHARMACOL EXP THER, V268, P1571
[7]   SUPEROXIDE RADICALS MEDIATE THE BIOCHEMICAL EFFECTS OF METHYLENEDIOXYMETHAMPHETAMINE (MDMA) - EVIDENCE FROM USING CUZN-SUPEROXIDE DISMUTASE TRANSGENIC MICE [J].
CADET, JL ;
LADENHEIM, B ;
HIRATA, H ;
ROTHMAN, RB ;
ALI, S ;
CARLSON, E ;
EPSTEIN, C ;
MORAN, TH .
SYNAPSE, 1995, 21 (02) :169-176
[8]   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
[9]   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
[10]   In vivo evidence for free radical involvement in the degeneration of rat brain 5-HT following administration of MDMA ('ecstasy') and p-chloroamphetamine but not the degeneration following fenfluramine [J].
Colado, MI ;
OShea, E ;
Granados, R ;
Murray, TK ;
Green, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1997, 121 (05) :889-900