A study of the effect of a single neurotoxic dose of 3,4-methylenedioxymethamphetamine (MDMA; "ecstasy") on the subsequent long-term behaviour of rats in the plus maze and open field

被引:52
作者
Mechan, AO
Moran, PM
Elliott, JM
Young, AMJ
Joseph, MH
Green, AR [1 ]
机构
[1] AstraZeneca R&D Charnwood, Loughborough LE11 5RH, Leics, England
[2] De Montfort Univ, Dept Pharmacol, Sch Pharm, Leicester LE1 9BH, Leics, England
[3] Univ Leicester, Sch Psychol, Leicester LE1 7RH, Leics, England
关键词
3,4-methylenedioxymethamphetarnine; MDMA; ecstasy; anxiety-related behaviour; elevated plus-maze; open field; long-term neurotoxicity;
D O I
10.1007/s002130100900
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale: Decreased 5-HT function has been shown to induce behaviour consistent with an "anxiolytic" effect. Administration of a single dose of 3,4-methylenedioxymethamphetamine (MDMA; "ecstasy" 12.5 mg/kg IP) to rats results in prolonged damage to central serotonergic nerve terminals. Thus we wished to assess whether an MDMA-induced lesion may have longer-term behavioural consequences. Objective: The study was designed to examine the behaviour of MDMA-pretreated and control animals in the elevated plus-maze and open field at a number of time-points, up to 80 days, after the administration of a single neurotoxic dose of MDMA (12.5 mg/kg IP). Results: MDMA-pretreated Dark Agouti rats demonstrated a statistically significant reduction in anxiety-related behaviour, compared to saline-pretreated control rats, in both the elevated plus-maze and open field when the rats were tested on day 73 (open field) and day 80 (plus maze) after MDMA administration. Conclusions: The behavioural consequences of a single neurotoxic dose of MDMA can be demonstrated over 2 months after administration of the compound, thereby indicating that long-term adaptive changes occur within the brain following the neurodegeneration of 5-HT neurones produced by this recreationally used drug.
引用
收藏
页码:167 / 175
页数:9
相关论文
共 71 条
[1]   MDMA ('Ecstasy') enhances 5-HT1A receptor density and 8-OH-DPAT-induced hypothermia:: blockade by drugs preventing 5-hydroxytryptamine depletion [J].
Aguirre, N ;
Ballaz, S ;
Lasheras, B ;
Del Rio, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 346 (2-3) :181-188
[2]  
Anderson IM, 1999, ADV EXP MED BIOL, V467, P43
[3]   Previous maze experience required to increase open arms avoidance in rats submitted to the elevated plus-maze model of anxiety [J].
Bertoglio, LJ ;
Carobrez, AP .
BEHAVIOURAL BRAIN RESEARCH, 2000, 108 (02) :197-203
[4]   EFFECT OF SEROTONERGIC LESION ON ANXIOUS BEHAVIOR MEASURED IN THE ELEVATED PLUS-MAZE TEST IN THE RAT [J].
BRILEY, M ;
CHOPIN, P ;
MORET, C .
PSYCHOPHARMACOLOGY, 1990, 101 (02) :187-189
[5]  
CALLAWAY CW, 1992, NEUROPSYCHOPHARMACOL, V7, P113
[6]  
CALLAWAY CW, 1990, J PHARMACOL EXP THER, V254, P456
[7]  
CALLAWAY CW, 1992, J PHARMACOL EXP THER, V263, P318
[8]   STIMULANT EFFECTS OF 3,4-METHYLENEDIOXYMETHAMPHETAMINE IN THE NUCLEUS-ACCUMBENS OF RAT [J].
CALLAWAY, CW ;
GEYER, MA .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1992, 214 (01) :45-51
[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]   5-HT LOSS IN RAT-BRAIN FOLLOWING 3,4-METHYLENEDIOXYMETHAMPHETAMINE (MDMA), P-CHLOROAMPHETAMINE AND FENFLURAMINE ADMINISTRATION AND EFFECTS OF CHLORMETHIAZOLE AND DIZOCILPINE [J].
COLADO, MI ;
MURRAY, TK ;
GREEN, AR .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :583-589