DOI, a 5-HT2A/2C receptor agonist, attenuates clozapine-induced cortical dopamine release

被引:46
|
作者
Ichikawa, J
Dai, J
Meltzer, HY
机构
[1] Vanderbilt Univ, Sch Med, Dept Psychiat, Div Psychopharmacol, Nashville, TN 37212 USA
[2] Vanderbilt Univ, Sch Med, Dept Pharmacol, Div Psychopharmacol, Nashville, TN 37212 USA
关键词
5-HT2A receptor; 5-HT1A receptor; DOI; clozapine; cortical dopamine release; microdialysis;
D O I
10.1016/S0006-8993(01)02596-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
(+/-)-1-(2,5-Dimethoxy-4-iodophenyl)-2-aminopropane hydrochloride (DOI, 1.25, 2.5 and 5 mg/kg), a serotonin (5-HT)(2A/2C) agonist, produced an inverted U-shaped increase in DA release in rat medial prefrontal cortex (mPFC) with a significant effect only at 2.5 mg/kg. This effect was completely abolished by M100907 (0.1 mg/kg), a 5-HT2A antagonist, and WAY100635 (0.2 mg/kg), a 5-HT1A antagonist, neither of which when given alone affected dopamine release. DOI (2.5 mg/kg), but not the 5-HT2C agonist Ro 60-0175 (3 mg/kg), attenuated clozapine (20 mg/kg)-induced mPFC dopamine release. These results suggest that 5-HT2A receptor stimulation increases basal cortical dopamine release via 5-HT1A receptor stimulation, and inhibits clozapine-induced conical dopamine release by diminishing 5-HT2A receptor blockade. (C) 2001 Published by Elsevier Science B.V.
引用
收藏
页码:151 / 155
页数:5
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