Lappalainen J, Hietala J, Koulu M, Syvälahti E
Department of Pharmacology, University of Turku, Finland.
Eur J Pharmacol. 1990 Nov 13;190(3):403-7. doi: 10.1016/0014-2999(90)94206-d.
The effects of chronic treatment with clozapine (20 mg/kg per day), ritanserin (0.5 mg/kg per day), haloperidol (0.5 mg/kg per day), or the combination of haloperidol and ritanserin, on dopamine (DA) and serotonin (5-HT) metabolism were studied. Chronic haloperidol treatment decreased DA metabolism in nucleus caudatus. Chronic ritanserin treatment failed to alter striatal or mesolimbic DA metabolism but decreased the concentrations of 5-HT and 5-hydroxyindoleacetic acid in the nucleus raphe dorsalis. The effects of chronic haloperidol were not altered by concomitant ritanserin administration. In comparison, chronic clozapine treatment affected neither DA nor 5-HT metabolism. These results show that the biochemical effects of chronic haloperidol treatment on the major ascending DA neurons cannot be modulated by concomitant 5-HT2 receptor blockade.
研究了氯氮平(每天20毫克/千克)、利坦色林(每天0.5毫克/千克)、氟哌啶醇(每天0.5毫克/千克)或氟哌啶醇与利坦色林联合长期治疗对多巴胺(DA)和5-羟色胺(5-HT)代谢的影响。长期氟哌啶醇治疗可降低尾状核中的DA代谢。长期利坦色林治疗未能改变纹状体或中脑边缘DA代谢,但降低了背侧中缝核中5-HT和5-羟吲哚乙酸的浓度。联合给予利坦色林不会改变长期氟哌啶醇的作用。相比之下,长期氯氮平治疗对DA和5-HT代谢均无影响。这些结果表明,5-HT2受体阻断剂不能调节长期氟哌啶醇治疗对主要上行DA神经元的生化作用。