Psychiatry Research Department, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Third Avenue, Harlow, Essex CM19 5AD, UK.
J Psychopharmacol. 1995 Jan;9(3):234-41. doi: 10.1177/026988119500900306.
The selective, brain penetrant, 5-HT(1D) receptor agonist SKF 99101H (10-30 mg/kg i.p.) caused a dose-related fall in rectal temperature in guinea pigs which lasted longer than 2 h. Sumatriptan (1.0-100 mg/kg i.p.), a selective 5-HT(1D) agonist which does not penetrate the brain, did not produce hypothermia, suggesting that peripheral mechanisms are not critically involved in the response. The hypothermia induced by SKF 99101H (30 mg/kg i.p.) was dose-dependently blocked by the 5-HT(1D) receptor antagonists GR 127935 (0.01-1 mg/kg i.p.) and GR 125743 (0.01-3 mg/kg i.p.), confirming the role of 5-HT(1D) receptors. Mianserin (0.3-10.0 mg/kg i.p.) and granisetron (0.1-3.0 mg/kg i.p.) were inactive, suggesting that 5-HT(2A/2B/2C) or 5-HT( 3) receptors play no significant role in the generation of the hypothermic response. Nor was the hypothermia reversed by prazosin (0.03-1.0 mg/kg i.p.), idazoxan (0.03-1.0 mg/kg i.p.) or scopolamine (0.01-0.3 mg/kg i.p.), thereby excluding mediation by α(1)- and α(2)-adrenoceptors and muscarinic receptors. WAY 100635 (0.1-1.0 mg/kg) significantly potentiated the effect of SKF 99101H. The antagonists, when given alone, had no effect on body temperature, with the exception of prazosin (0.1 and 1.0 mg/kg). Three days of treatment with parachloroamphetamine (30 mg/kg i.p.) depleted forebrain 5-HT by ∼ 75% in frontal cortex, hypothalamus, hippocampus and striatum, but failed to alter the hypothermic response to SKF 99101H. The hypothermia is, therefore, unlikely to be mediated by 5-HT(1D) receptors located on 5-HT neurons. SKF 99101H-induced hypothermia in the guinea pig may serve as a useful model for investigation of centrally acting 5-HT( 1D) receptor antagonists.
选择性、穿透血脑屏障的 5-HT(1D) 受体激动剂 SKF 99101H(10-30mg/kg 腹腔注射)引起豚鼠直肠温度呈剂量相关性下降,持续时间超过 2 小时。舒马曲坦(1.0-100mg/kg 腹腔注射),一种不穿透大脑的选择性 5-HT(1D) 激动剂,不会引起体温过低,表明外周机制与反应无关。SKF 99101H(30mg/kg 腹腔注射)引起的体温过低剂量依赖性地被 5-HT(1D) 受体拮抗剂 GR 127935(0.01-1mg/kg 腹腔注射)和 GR 125743(0.01-3mg/kg 腹腔注射)阻断,证实了 5-HT(1D) 受体的作用。米氮平(0.3-10.0mg/kg 腹腔注射)和格兰司琼(0.1-3.0mg/kg 腹腔注射)无活性,表明 5-HT(2A/2B/2C)或 5-HT(3)受体在产生体温过低反应中不起重要作用。普萘洛尔(0.03-1.0mg/kg 腹腔注射)、伊达唑(0.03-1.0mg/kg 腹腔注射)或东莨菪碱(0.01-0.3mg/kg 腹腔注射)也不能逆转体温过低,从而排除了α(1)-和α(2)-肾上腺素能受体和毒蕈碱受体的介导。WAY 100635(0.1-1.0mg/kg)显著增强 SKF 99101H 的作用。拮抗剂单独使用时对体温没有影响,除了普萘洛尔(0.1 和 1.0mg/kg)。3 天用对氯苯丙胺(30mg/kg 腹腔注射)处理,使前额皮质、下丘脑、海马和纹状体中的 5-HT 减少约 75%,但不能改变 SKF 99101H 引起的体温过低反应。因此,这种体温过低不太可能是由位于 5-HT 神经元上的 5-HT(1D) 受体介导的。SKF 99101H 引起的豚鼠体温过低可能是一种研究中枢作用 5-HT(1D) 受体拮抗剂的有用模型。