Cullen L K, Reynoldson J A
School of Veterinary Studies, Murdoch University, Western Australia.
J Vet Pharmacol Ther. 1990 Mar;13(1):86-92. doi: 10.1111/j.1365-2885.1990.tb00752.x.
The aim of this study was to determine the contribution of alpha 2- and alpha 1-adrenoceptor agonist activity of the formamidine, amitraz, on peripheral circulation in the dog. Intra-arterial injections of amitraz (0.25-5.0 micrograms/kg) produced a dose-dependent increase in perfusion pressure in the autoperfused hind limbs of methoxyflurane-anaesthetized dogs. A constant blood flow to the hind limbs was maintained using a peristaltic pump. Intravenous phentolamine (0.5 mg/kg), prazosin (35 micrograms/kg) and yohimbine (10 micrograms/kg) in separate experiments antagonized the vasoconstrictor actions of amitraz and produced a parallel shift to the right of the amitraz dose-response curve. Cumulative doses of amitraz (0.5-15 micrograms/kg) given by intracisterna magna (i.c.m.) injections reduced mean arterial pressure and heart rate in a dose-dependent manner. Similar responses were produced by intravenous amitraz but at much higher doses. In separate experiments amitraz-induced hypotension (doses up to 25 micrograms/kg i.c.m.) was prevented by pre-treatment with yohimbine (30 micrograms/kg i.c.m.) but not prazosin (20 micrograms/kg i.c.m.). Both antagonists partially inhibited the bradycardia produced by amitraz. It is concluded that amitraz stimulates alpha 1- and alpha 2-adrenoceptors to produce vascular constriction. The central hypotensive action of amitraz appears to be mediated by alpha 2-adrenoceptors; however, both receptor subtypes appear to be stimulated to produce bradycardia.
本研究的目的是确定甲脒类药物双甲脒的α2 -和α1 -肾上腺素能受体激动活性对犬外周循环的作用。在甲氧氟烷麻醉的犬的自灌注后肢中,动脉内注射双甲脒(0.25 - 5.0微克/千克)可使灌注压呈剂量依赖性升高。使用蠕动泵维持后肢恒定的血流量。在单独的实验中,静脉注射酚妥拉明(0.5毫克/千克)、哌唑嗪(35微克/千克)和育亨宾(10微克/千克)可拮抗双甲脒的血管收缩作用,并使双甲脒剂量 - 反应曲线向右平行移动。经小脑延髓池(i.c.m.)注射双甲脒的累积剂量(0.5 - 15微克/千克)可使平均动脉压和心率呈剂量依赖性降低。静脉注射双甲脒也产生类似反应,但所需剂量更高。在单独的实验中,育亨宾(30微克/千克i.c.m.)预处理可预防双甲脒诱导的低血压(剂量高达25微克/千克i.c.m.),但哌唑嗪(20微克/千克i.c.m.)则不能。两种拮抗剂均部分抑制双甲脒引起的心动过缓。结论是双甲脒刺激α1 -和α2 -肾上腺素能受体产生血管收缩。双甲脒的中枢性降压作用似乎由α2 -肾上腺素能受体介导;然而,两种受体亚型似乎均被刺激而产生心动过缓。