Antipsychotic drugs classified by their effects on the release of dopamine and noradrenaline in the prefrontal cortex and striatum

被引:102
作者
Westerink, BHC
Kawahara, Y
De Boer, P
Geels, C
De Vries, JB
Wikström, HV
Van Kalkeren, A
Van Vliet, B
Kruse, CG
Long, SK
机构
[1] Univ Groningen, Ctr Pharm, Dept Med Chem, NL-9713 AV Groningen, Netherlands
[2] Solvay Pharmaceut, NL-1380 DA Weesp, Netherlands
关键词
antipsychotic drug; prefrontal cortex; striatum;
D O I
10.1016/S0014-2999(00)00935-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dose-effect curves were established for the effects of the antipsychotic drugs haloperidol, clozapine, olanzapine, risperidone and ziprasidone on extracellular levels of dopamine and noradrenaline in the medial prefrontal cortex, and of dopamine in the striatum. Haloperidol was more effective in stimulating the release of dopamine in the striatum, whereas clozapine was much more effective in the medial prefrontal cortex. The efficacy of risperidone, olanzapine and ziprasidone did not differ for the two brain areas. The benzamides sulpiride and raclopride increased dopamine release in the striatum but did not affect the release of dopamine and noradrenaline in the medial prefrontal cortex. In the presence of dopamine/noradrenaline reuptake inhibitors, the benzamides strongly increased the release of dopamine-but not of noradrenaline-in the medial prefrontal cortex. The 5-HT2 receptor antagonist R-(+)-alpha-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol (MDL100,907) (800 nmol/kg) and the dopamine D-2 receptor antagonist raclopride (2 mu mol/kg) displayed a clear synergism in increasing the release of dopamine in the medial prefrontal cortex. No such synergism was seen in the case of noradrenaline. Go-administration of the 5-HT2 receptor agonist (+)-2,5-dimethoxy-4-iodoamphetamine HCl (DOI) (850 nmol/kg) with clozapine (10 mu mol/kg) or haloperidol(800 nmol/kg) blocked the increase in dopamine as well as noradrenaline in the medial prefrontal cortex. It is concluded that typical and non-benzamide atypical antipsychotics increase extracellular dopamine in the medial prefrontal cortex via a synergistic interaction by blocking 5-HT2 as well as dopamine D-2 receptors. The increase in extracellular noradrenaline in the medial prefrontal cortex that was observed after administration of antipsychotics is explained by inhibition of 5-HT2 receptors and not dopamine D-2 receptors. Finally, the significance of the classification of antipsychotic drugs based on their selective action on the release of dopamine and noradrenaline in the medial prefrontal cortex is discussed. In particular, the position of the benzamides is discussed. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
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页码:127 / 138
页数:12
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