Association of caffeine to MDMA does not increase antinociception but potentiates adverse effects of this recreational drug

被引:30
作者
Camarasa, Jordi [1 ]
Pubill, David [1 ]
Escubedo, Elena [1 ]
机构
[1] Univ Barcelona, Fac Farm, Unit Farmacol & Farmacognosia, E-08028 Barcelona, Spain
关键词
MDMA; caffeine; rat; neurotoxicity; antinociception;
D O I
10.1016/j.brainres.2006.06.087
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ecstasy (MDMA) street tablets often contain several other compounds in addition to MDMA, particularly caffeine. Then, it becomes necessary to study the consequences of caffeine plus MDMA combination. MDMA (1 mg/kg) elicited an analgesic response both at the spinal and supraspinal levels. However, when associated, MDMA and caffeine did not show any synergistic interaction. When caffeine was administered prior to MDMA, a potentiation of locomotor activity was observed, which consisted in an increase in maximal values and in a prolonged time of activity. In the neurotoxicity studies, a hyperthermic effect of MDMA was observed. Although caffeine alone failed to alter body temperature, it potentiated MDMA-induced hyperthermia. This association also significantly increased MDMA lethality (from 22% to 34%). Following administration of MDMA to rats, there was a persistent decrease in the number of serotonin transporter sites in the cortex, striatum and hippocampus, which was potentiated by caffeine cotreatment. This MDMA toxicity in rats was accompanied by a transient dopaminergic impairment in the striatum, measured as decreased [H-3]WIN35428 binding sites, by 31% 3 days after treatment, which was not modified by caffeine. A transient down-regulation of 5-HT2 receptors occurred in the cortex of MDMA-treated rats, whose recovery was slowed by co-treatment with caffeine. In conclusion, the association of MDMA with caffeine does not generate any beneficial effects at the antinociceptive level. The acute effects stemming from this association, in tandem with the final potentiation of serotonergic terminals injury, provide evidence of the potentially greater long-term adverse effects of this particular recreational drug combination. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 82
页数:11
相关论文
共 44 条
[1]   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
[2]  
BATTAGLIA G, 1987, J PHARMACOL EXP THER, V242, P911
[3]   Effect of 3,4-methylendioxymethamphetamine (MDMA, "ecstasy") on dopamine transmission in the nucleus accumbens shell and core [J].
Cadoni, C ;
Solinas, M ;
Pisanu, A ;
Zernig, G ;
Acquas, E ;
Di Chiara, G .
BRAIN RESEARCH, 2005, 1055 (1-2) :143-148
[4]   Acute and long-term effects of MDMA on cerebral dopamine biochemistry and function [J].
Colado, MI ;
O'Shea, E ;
Green, AR .
PSYCHOPHARMACOLOGY, 2004, 173 (3-4) :249-263
[5]   3,4-N-methlenedioxymethamphetamine-induced hypophagia is maintained in 5-HT1B receptor knockout mice, but suppressed by the 5-HT2C receptor antagonist RS102221 [J].
Conductier, G ;
Crosson, C ;
Hen, R ;
Bockaert, J ;
Compan, V .
NEUROPSYCHOPHARMACOLOGY, 2005, 30 (06) :1056-1063
[6]   THE ANTINOCICEPTIVE EFFECTS OF 3,4-METHYLENEDIOXYMETHAMPHETAMINE (MDMA) IN THE RAT [J].
CRISP, T ;
STAFINSKY, JL ;
BOJA, JW ;
SCHECHTER, MD .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1989, 34 (03) :497-501
[7]   Microgliosis and down-regulation of adenosine transporter induced by methamphetamine in rats [J].
Escubedo, E ;
Guitart, L ;
Sureda, FX ;
Jiménez, A ;
Pubill, D ;
Pallàs, M ;
Camins, A ;
Camarasa, J .
BRAIN RESEARCH, 1998, 814 (1-2) :120-126
[8]   ADENOSINE DOPAMINE INTERACTIONS IN THE BRAIN [J].
FERRE, S ;
FUXE, K ;
VONEULER, G ;
JOHANSSON, B ;
FREDHOLM, BB .
NEUROSCIENCE, 1992, 51 (03) :501-512
[9]  
Fredholm BB, 1999, PHARMACOL REV, V51, P83
[10]   Caffeine induces central cholinergic analgesia [J].
Ghelardini, C ;
Galeotti, N ;
Bartolini, A .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1997, 356 (05) :590-595