Skingle M, Higgins G A, Feniuk W
Department of Neuropharmacology, Glaxo Group Research, Ware, Hertfordsire SG12 ODP.
J Psychopharmacol. 1994 Jan;8(1):14-21. doi: 10.1177/026988119400800103.
The 5-HT(1) receptor agonist GR46611 (3-30 mg/kg s.c.) caused a dose-related decrease in rectal temperature in the adult guinea-pig. A lower dose (20 μg) administered directly into the lateral cerebral ventricle also caused a hypothermic response, suggesting that this effect is centrally mediated. GR46611-induced (10 mg/kg s.c.) hypothermia was not attenuated by WAY100135 (3-10 mg/kg s.c.), ritanserin (0.3-1 mg/kg s.c.), spiperone (0.1-0.3 mg/kg s.c.) and ondansetron (0.1-1 mg/kg s.c.), suggesting that 5-HT(1A), 5-HT(2A), 5-HT( 2C) and 5-HT(3) receptors are unlikely to be involved in this response. In contrast, the poorly selective 5-HT receptor antagonist, metergoline (1-10 mg/kg s.c.), and the potent 5-HT(1D) receptor antagonist, GR127935 (0.1-1 mg/kg p.o.), antagonized the effects of GR46611. The present data suggest that antagonism of GR46611-induced hypothermia may be useful for assessing the potency and duration of action of centrally-acting 5-HT( 1D) receptor antagonists in the guinea-pig.
5-羟色胺(5-HT)1受体激动剂GR46611(皮下注射3 - 30毫克/千克)可使成年豚鼠的直肠温度呈剂量依赖性下降。直接向侧脑室注射较低剂量(20微克)也会引起体温过低反应,表明这种效应是由中枢介导的。GR46611诱导的(皮下注射10毫克/千克)体温过低并未被WAY100135(皮下注射3 - 10毫克/千克)、利坦色林(皮下注射0.3 - 1毫克/千克)、螺哌隆(皮下注射0.1 - 0.3毫克/千克)和昂丹司琼(皮下注射0.1 - 1毫克/千克)减弱,这表明5-HT1A、5-HT2A、5-HT2C和5-HT3受体不太可能参与此反应。相比之下,选择性较差的5-HT受体拮抗剂麦角乙脲(皮下注射1 - 10毫克/千克)和强效5-HT1D受体拮抗剂GR127935(口服0.1 - 1毫克/千克)可拮抗GR46611的作用。目前的数据表明,拮抗GR46611诱导的体温过低可能有助于评估豚鼠体内中枢作用的5-HT1D受体拮抗剂的效力和作用持续时间。