Increased CRE-binding activity and tryptophan hydroxylase mRNA expression induced by 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") in the rat frontal cortex but not in the hippocampus

被引:19
|
作者
García-Osta, A [1 ]
Del Río, J [1 ]
Frechilla, D [1 ]
机构
[1] Univ Navarra, Sch Med, Dept Pharmacol, E-31080 Pamplona, Spain
来源
MOLECULAR BRAIN RESEARCH | 2004年 / 126卷 / 02期
关键词
MDMA; amphetamine; tryptophan hydroxylase; DNA binding; CREB;
D O I
10.1016/j.molbrainres.2004.04.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A single administration of either 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") or p-chloroamphetamine (PCA) produced a rapid and marked reduction of serotonin (5-HT) content in rat frontal cortex and hippocampus. In the cortex of MDMA-treated rats, 5-HT levels returned to control values 48 h after drug administration. This recovery was correlated with an induction of CRE-binding activity and an enhanced expression of tryptophan hydroxylase (TPH) mRNA, the rate-limiting enzyme in 5-HT biosynthesis, suggesting that MDMA may up-regulate the TPH gene through a CREB-dependent mechanism. In the cortex of PCA-treated rats, neither a recovery of 5-HT levels nor changes in DNA-binding or TPH mRNA were found at the same time point. In the hippocampus of rats receiving either PCA or MDMA a decrease in TPH mRNA levels was found at all times, along with a reduced CRE-binding at the 8-h time point. The results show region-specific effects of MDMA. In the frontal cortex, the increased TPH expression suggests a compensatory response to MDMA-induced loss of serotonergic function. (C) 2004 Elsevier B.V. All rights reserved.
引用
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页码:181 / 187
页数:7
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