Nagashima M, Yamada K, Kimura H, Matsumoto S, Furukawa T
Department of Pharmacology, School of Medicine, Fukuoka University, Japan.
Pharmacol Biochem Behav. 1992 Dec;43(4):993-7. doi: 10.1016/0091-3057(92)90472-r.
The present experiments were performed to investigate the effects of dopamine D1 receptor agonists given alone or in combination with dopamine D2 receptor agonists on body temperature in rats. The selective dopamine D1 receptor agonist, 1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepine-7,8-diol (SK&F38393), produced hyperthermia. However, the dopamine D2 receptor agonist, B-HT 920 (talipexole), and the newly synthesized dopamine D2 receptor agonist, (S)-2-amino-4,5,6,7-tetrahydro-6-propylamino-benzothiazole (SND 919), did not change the temperature. Interestingly, the SK&F38393-induced hyperthermia was enhanced by talipexole and SND 919. The drastic hyperthermia induced by combined administration of dopamine D1 and D2 receptor agonists was blocked by either the dopamine D1 receptor antagonist, SCH23390, or the dopamine D2 receptor antagonist, spiperone. On the other hand, treatment with prazosin, yohimbine, propranolol, scopolamine, or methysergide failed to affect the marked hyperthermia. The present results suggest that a functional link between dopamine D1 and D2 receptors may be synergistic in the regulation of body temperature and that concurrent stimulation of both dopamine D1 and D2 receptors thereby produces marked hyperthermia in the rat.
进行本实验以研究单独给予多巴胺D1受体激动剂或与多巴胺D2受体激动剂联合使用对大鼠体温的影响。选择性多巴胺D1受体激动剂1-苯基-2,3,4,5-四氢-(1H)-3-苯并氮杂卓-7,8-二醇(SK&F38393)可引起体温升高。然而,多巴胺D2受体激动剂B-HT 920(他利克索)和新合成的多巴胺D2受体激动剂(S)-2-氨基-4,5,6,7-四氢-6-丙基氨基-苯并噻唑(SND 919)并未改变体温。有趣的是,他利克索和SND 919增强了SK&F38393诱导的体温升高。多巴胺D1和D2受体激动剂联合给药引起的剧烈体温升高可被多巴胺D1受体拮抗剂SCH23390或多巴胺D2受体拮抗剂螺哌隆阻断。另一方面,用哌唑嗪、育亨宾、普萘洛尔、东莨菪碱或甲基麦角新碱治疗未能影响明显的体温升高。目前的结果表明,多巴胺D1和D2受体之间的功能联系在体温调节中可能具有协同作用,同时刺激多巴胺D1和D2受体从而在大鼠中产生明显的体温升高。