Sánchez C
Pharmacological Research, H. Lundbeck A/S, Copenhagen-Valby, Denmark.
Eur J Pharmacol. 1989 Nov 21;171(2-3):201-6. doi: 10.1016/0014-2999(89)90108-8.
The effect of dopamine D-1 and D-2 receptor stimulation on body temperature has been investigated in male mice. The selective D-2 receptor agonists, quinpirole and LY 163502, and the mixed D-1/D-2 agonist, apomorphine, induced a dose-dependent hypothermia, whereas the selective D-1 receptor agonists, SK&F 81297, SK&F 38393 and SK&F 75670, induced hyperthermia. The hyperthermic responses of these agents were of a similar magnitude although the relative efficacies determined in vitro with the adenylate cyclase assay were different. The peripherally acting D-1 agonist, fenoldopam, did not influence body temperature, indicating that the hyperthermia is mediated, centrally. Studies with combinations of quinpirole and SK&F 38393 showed that the effect of one of the substances could be counteracted by the other. Furthermore, antagonist studies showed that the hypothermia induced by quinpirole could be inhibited by the D-2-selective antagonist, YM 09151-2, and by the mixed D-1/D-2 antagonist, cis(Z)-flupentixol, but not by the D-1-selective antagonist, SCH 23390. Similar results were found for apomorphine-induced hypothermia. SK&F 38393-induced hyperthermia could be antagonized by all three antagonists. These results suggest that the two receptor subtypes act differentially on body temperature, and that they influence a common out-put system, but in opposite directions. These findings are opposite to those of behavioural studies, where a synergistic function of D-1 and D-2 receptors has been demonstrated in the regulation of motor function.
已在雄性小鼠中研究了多巴胺D - 1和D - 2受体刺激对体温的影响。选择性D - 2受体激动剂喹吡罗和LY 163502,以及混合性D - 1/D - 2激动剂阿扑吗啡,均可诱导剂量依赖性体温降低,而选择性D - 1受体激动剂SK&F 81297、SK&F 38393和SK&F 75670则可诱导体温升高。尽管通过腺苷酸环化酶测定法在体外确定的相对效力不同,但这些药物的体温升高反应幅度相似。外周作用的D - 1激动剂非诺多泮对体温无影响,表明体温升高是由中枢介导的。喹吡罗与SK&F 38393联合使用的研究表明,其中一种物质的作用可被另一种物质抵消。此外,拮抗剂研究表明,喹吡罗诱导的体温降低可被D - 2选择性拮抗剂YM 09151 - 2和混合性D - 1/D - 2拮抗剂顺式(Z) - 氟哌噻吨抑制,但不能被D - 1选择性拮抗剂SCH 23390抑制。阿扑吗啡诱导的体温降低也得到了类似结果。SK&F 38393诱导的体温升高可被所有三种拮抗剂拮抗。这些结果表明,两种受体亚型对体温的作用不同,它们影响一个共同的输出系统,但方向相反。这些发现与行为学研究结果相反,在行为学研究中,已证明D - 1和D - 2受体在运动功能调节中具有协同作用。