Nolan A, Livingston A, Waterman A
Department of Pharmacology, Medical School, Bristol, U.K.
J Vet Pharmacol Ther. 1987 Sep;10(3):202-9. doi: 10.1111/j.1365-2885.1987.tb00530.x.
The antinociceptive activity of the intravenously administered alpha 2-adrenoceptor agonists, clonidine and xylazine, was measured in sheep using thermal and mechanical pressure threshold detection systems. Both drugs demonstrated clear antinociceptive activity for both forms of threshold stimuli and clonidine at 6 micrograms/kg i.v. was more potent and longer lasting than xylazine at 50 micrograms/kg i.v. The antinociceptive effects were reversed by idazoxan (0.1 mg/kg i.v.), but were not affected by naloxone at 0.2 mg/kg i.v. indicating that these effects were mediated by alpha 2-adrenoceptors.
采用热和机械压力阈值检测系统,在绵羊中测定静脉注射α₂ - 肾上腺素能受体激动剂可乐定和赛拉嗪的抗伤害感受活性。两种药物对两种形式的阈值刺激均表现出明显的抗伤害感受活性,静脉注射6微克/千克的可乐定比静脉注射50微克/千克的赛拉嗪更有效且作用更持久。抗伤害感受作用可被静脉注射的咪唑克生(0.1毫克/千克)逆转,但不受静脉注射0.2毫克/千克纳洛酮的影响,这表明这些作用是由α₂ - 肾上腺素能受体介导的。