Yamada S, Harano M, Yokoo H, Tanaka M
Institute of Brain Diseases, Kurume University School of Medicine, Fukuoka, Japan.
J Pharm Pharmacol. 1997 Feb;49(2):206-8. doi: 10.1111/j.2042-7158.1997.tb06780.x.
The effects of a newly synthesized quinolinone derivative, 7-[4-(4-(2,3-dichlorophenyl)-1-piperazinyl) butoxy)-3,4-dihydro-2-(1H)-quinolinone (OPC-14597), a novel antipsychotic drug, on electrically evoked dopamine release in rat striatal slices were investigated. OPC-14597 (0.1-10 microM) had no effect on the dopamine release evoked in the striatal slices. The decrease induced by quinpirole, a dopamine receptor agonist, in evoked dopamine release was attenuated by superfusion with OPC-14597 (1 and 10 microM) which by itself had no effect on evoked dopamine release. The increase induced by (-)-sulpiride, a dopamine receptor antagonist, in evoked dopamine release was, moreover, also attenuated by 1 and 10 microM OPC-14597. These findings indicate that OPC-14597 antagonizes both dopamine agonist- and antagonist-induced changes in evoked dopamine release in striatal slices in rats.
研究了一种新合成的喹啉酮衍生物7-[4-(4-(2,3-二氯苯基)-1-哌嗪基)丁氧基]-3,4-二氢-2-(1H)-喹啉酮(OPC-14597),一种新型抗精神病药物,对大鼠纹状体切片中电诱发多巴胺释放的影响。OPC-14597(0.1 - 10微摩尔)对纹状体切片中诱发的多巴胺释放没有影响。多巴胺受体激动剂喹吡罗诱导的诱发多巴胺释放的减少,通过用OPC-14597(1和10微摩尔)灌注而减弱,而OPC-14597本身对诱发的多巴胺释放没有影响。此外,多巴胺受体拮抗剂(-)-舒必利诱导的诱发多巴胺释放的增加,也被1和10微摩尔的OPC-14597减弱。这些发现表明,OPC-14597拮抗多巴胺激动剂和拮抗剂诱导的大鼠纹状体切片中诱发多巴胺释放的变化。