Rivest R, Marsden C A
Department of Pharmacology, Medical School, University of Sherbrooke, Quebec, Canada.
Synapse. 1992 Jan;10(1):71-8. doi: 10.1002/syn.890100110.
This study compares the effects of the nonamphetamine stimulant amfonelic acid on the increase in extracellular 3,4-dihydroxyphenylacetic acid (DOPAC) induced by haloperidol and clozapine in the nucleus accumbens and the striatum of anaesthetized rats. DOPAC was simultaneously recorded in both regions using differential pulse voltammetry with electrically pretreated carbon fibre electrodes. Amfonelic acid (2.5 mg/kg s.c.) did not alter basal striatal DOPAC but produced a significant reduction in extracellular DOPAC in the nucleus accumbens. Haloperidol (1 mg/kg s.c.) increased extracellular DOPAC in both regions. When amfonelic acid was injected 5 min before haloperidol, the increase in DOPAC was potentiated in both the nucleus accumbens and the striatum but with a greater effect in the striatum. Clozapine (30 mg/kg i.p.) increased extracellular DOPAC in both regions, an effect partially attenuated by amfonelic acid in both regions but to a greater extent in the striatum. When ritanserin (5 mg/kg i.p.), a serotonergic antagonist (5-HT-2), was co-administered with haloperidol, the potentiation by amfonelic acid of the increase in extracellular DOPAC induced by haloperidol was attenuated in both the nucleus accumbens and the striatum. The present results confirm that amfonelic acid can be used to discriminate neurochemically between haloperidol and clozapine in vivo. The effects of amfonelic acid on the neuroleptic-induced changes in extracellular DOPAC were greater in the striatum than the nucleus accumbens. These results further demonstrate that both neuroleptics increase dopamine metabolism in the two brain regions but by different mechanisms, supporting the view that the regulation of dopamine metabolism differs in the two regions.(ABSTRACT TRUNCATED AT 250 WORDS)
本研究比较了非苯丙胺类兴奋剂安非他明酸对氟哌啶醇和氯氮平在麻醉大鼠伏隔核和纹状体中诱导的细胞外3,4-二羟基苯乙酸(DOPAC)增加的影响。使用经电预处理的碳纤维电极,通过差分脉冲伏安法同时记录两个区域的DOPAC。安非他明酸(2.5mg/kg皮下注射)不改变纹状体基础DOPAC,但使伏隔核细胞外DOPAC显著降低。氟哌啶醇(1mg/kg皮下注射)使两个区域的细胞外DOPAC增加。当在氟哌啶醇注射前5分钟注射安非他明酸时,伏隔核和纹状体中DOPAC的增加均被增强,但在纹状体中的作用更大。氯氮平(30mg/kg腹腔注射)使两个区域的细胞外DOPAC增加,安非他明酸在两个区域均部分减弱了该作用,但在纹状体中减弱程度更大。当5-羟色胺拮抗剂利坦色林(5mg/kg腹腔注射)与氟哌啶醇共同给药时,安非他明酸对氟哌啶醇诱导的细胞外DOPAC增加的增强作用在伏隔核和纹状体中均减弱。目前的结果证实,安非他明酸可用于在体内从神经化学角度区分氟哌啶醇和氯氮平。安非他明酸对神经阻滞剂诱导的细胞外DOPAC变化的影响在纹状体中比在伏隔核中更大。这些结果进一步证明,两种神经阻滞剂均通过不同机制增加两个脑区的多巴胺代谢,支持两个区域中多巴胺代谢调节不同的观点。(摘要截短至250字)