Learning and memory after neonatal exposure to 3,4-methylenedioxymethamphetamine (Ecstasy) in rats: Interaction with exposure in adulthood

被引:34
作者
Cohen, MA
Skelton, MR
Schaefer, TL
Gudelsky, GA
Vorhees, CV
Williams, MT
机构
[1] Cincinnati Childrens Res Fdn, Div Neurol, MLC 7044, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Cincinnati, OH 45229 USA
[3] Univ Cincinnati, Coll Pharm, Cincinnati, OH 45267 USA
关键词
MDMA; development; amphetamines; serotonin; dopamine; spatial learning; preclinical;
D O I
10.1002/syn.20166
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study determined whether developmental and adult 3,4-methylenedioxymethamphetamine (MDMA) exposures in rats have interactive effects on body temperature, learning, other behaviors, and monoamine concentrations in the hippocampus, prefrontal cortex, and striatum. Learning was assessed in the Cincinnati water maze (CWM), Morris water maze (MWM), and novel object recognition (NOR). On acquisition trials in the MWM, significant differences from developmental MDMA exposure were found on latency, cumulative distance, path length, and angle of first bearing to the goal, but the early and adult MDMA exposure group performed no worse than the developmental-only MDMA group. In the reversal trials, however, an interaction was seen: latency to the goal, cumulative distance, and angle of first bearing were increased in animals treated both developmentally and in adulthood with MDMA compared with those treated only developmentally. Other tests (elevated zero maze, CWM, NOR, and open-field activity) did not show an interaction, nor did hippocampal concentrations of serotonin or dopamine. However, several behavioral tests showed neonatal MDMA effects, including increased errors in the CWM, reduced time spent with a new object in the NOR test, and reduced locomotor activity in the open-field. By contrast, adult MDMA decreased the number of entries into open quadrants of the elevated zero maze. Litter effects were controlled by treating litter as the experimental unit and using mixed models repeated measures analyses. Correlational analyses suggested that the MWM reversal interaction involves multiple monoamine changes. The results indicate that developmental MDMA exposure can interact with adult exposure to interfere with some aspects of learning. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:148 / 159
页数:12
相关论文
共 53 条
[1]  
BAYER SA, 1993, NEUROTOXICOLOGY, V14, P83
[2]   3,4-Methylenedioxymethamphetamine (ecstasy)-induced learning and memory impairments depend on the age of exposure during early development [J].
Broening, HW ;
Morford, LL ;
Inman-Wood, SL ;
Fukumura, M ;
Vorhees, CV .
JOURNAL OF NEUROSCIENCE, 2001, 21 (09) :3228-3235
[3]  
BROENING HW, 1995, J PHARMACOL EXP THER, V275, P325
[4]   Decreased social behaviour following 3,4-methylenedioxymethamphetamine (MDMA) is accompanied by changes in 5-HT2A receptor responsivity [J].
Bull, EJ ;
Hutson, PH ;
Fone, KCF .
NEUROPHARMACOLOGY, 2004, 46 (02) :202-210
[5]  
Clark RE, 2000, J NEUROSCI, V20, P8853
[6]   The pre-clinical behavioural pharmacology of 3,4-methylenedioxymethamphetamine (MDMA) [J].
Cole, JC ;
Sumnall, HR .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2003, 27 (03) :199-217
[7]   Effects of MDMA exposure on the conditioned place preference produced by other drugs of abuse [J].
Cole, JC ;
Sumnall, HR ;
O'Shea, E ;
Marsden, CA .
PSYCHOPHARMACOLOGY, 2003, 166 (04) :383-390
[8]   Contribution of cannabis and MDMA ("ecstasy") to cognitive changes in long-term polydrug users [J].
Dafters R.I. ;
Hoshi R. ;
Talbot A.C. .
Psychopharmacology, 2004, 173 (3-4) :405-410
[9]   Dopamine-mediated stabilization of delay-period activity in a network model of prefrontal cortex [J].
Durstewitz, D ;
Seamans, JK ;
Sejnowski, TJ .
JOURNAL OF NEUROPHYSIOLOGY, 2000, 83 (03) :1733-1750
[10]   A NEW ONE-TRIAL TEST FOR NEUROBIOLOGICAL STUDIES OF MEMORY IN RATS .3. SPATIAL VS NONSPATIAL WORKING MEMORY [J].
ENNACEUR, A ;
MELIANI, K .
BEHAVIOURAL BRAIN RESEARCH, 1992, 51 (01) :83-92