Fink H, Morgenstern R, Oelssner W
Pharmacol Biochem Behav. 1984 Apr;20(4):513-7. doi: 10.1016/0091-3057(84)90297-1.
The effect of clozapine on the central serotonergic transmission system was studied by investigation of open-field motility of rats after microinjection of drugs into nucleus accumbens and median raphe nucleus. Previous work has shown that LSD in low doses potentiates apomorphine-induced hypermotility and that this LSD effect is induced by a serotonin agonist action in median raphe nucleus. Clozapine, injected into median raphe nucleus (0.05 micrograms), suppressed the LSD effect in the same manner as serotonin antagonists did. Since alpha-adrenergic drugs, injected into median raphe nucleus, caused locomotor stimulant effects, an alpha- adrenalytic action of clozapine was excluded. Clozapine, injected into nucleus accumbens (0.2 micrograms), increased apomorphine-induced hypermotility, whereas the dopamine antagonist haloperidol suppressed it. Our results suggest a serotonin antagonist action of clozapine.
通过向大鼠伏隔核和中缝核微量注射药物后观察旷场活动,研究了氯氮平对中枢5-羟色胺能传递系统的影响。先前的研究表明,低剂量的麦角酸二乙胺(LSD)可增强阿扑吗啡诱导的活动亢进,且这种LSD效应是由中缝核中的5-羟色胺激动剂作用所诱导。向中缝核注射氯氮平(0.05微克),其抑制LSD效应的方式与5-羟色胺拮抗剂相同。由于向中缝核注射α-肾上腺素能药物会产生运动兴奋作用,因此排除了氯氮平的α-肾上腺素能阻断作用。向伏隔核注射氯氮平(0.2微克)可增强阿扑吗啡诱导的活动亢进,而多巴胺拮抗剂氟哌啶醇则抑制该作用。我们的结果提示氯氮平具有5-羟色胺拮抗剂作用。