Queiroz-Neto A, Zamur G, Gonçalves S C, Carregaro A B, Mataqueiro M I, Harkins J D, Tobin T
Faculdade de Ciências Agrárias e Veterinárias, Câmpus de Jaboticabal, FCAV/UNESP, SP, Brazil.
J Vet Pharmacol Ther. 1998 Oct;21(5):400-5. doi: 10.1046/j.1365-2885.1998.00150.x.
Amitraz, an acaricide used to control ectoparasites in animals has a complex pharmacological activity, including alpha2-adrenergic agonist action. The purpose of this research was to investigate the possible antinociceptive and/or sedative effect of amitraz in horses. The sedative effect of the intravenous (i.v.) injection of dimethylformamide (DMF, 5 mL, control) or amitraz (0.05, 0.10, 0.15 mg/kg), was investigated on the head ptosis test. The participation of alpha2-adrenergic receptors in the sedative effect provoked by amitraz was studied by dosing yohimbine (0.12 mg/kg, i.v.). To measure the antinociception, xylazine hydrochloride (1 mg/kg, i.v., positive control) and the same doses of amitraz and DMF were used. A focused radiant light/heat directed onto the fetlock and withers of a horse were used as a noxious stimulus to measure the hoof withdrawal reflex latency (HWRL) and the skin twitch reflex latency (STRL). The three doses of amitraz used (0.05, 0.10 and 0.15 mg/kg) provoked a dose-dependent relaxation of the cervical muscles. The experiments with amitraz and xylazine on the HWRL showed that after i.v. administration of all doses of amitraz there was a significant increase of HWRL up to 150 min after the injections. Additionally, there was a significant difference between control (DMF) and positive control (xylazine) values up to 30 min after drug injection. On the other hand, the experiments on the STRL show that after administration of amitraz at the dose of 0.15 mg/kg, a significant increase in STRL was observed when compared with the control group. This effect lasted up to 120 min after injection. However, no significant antinociceptive effect was observed with the 0.05 and 0.10 mg/kg doses of amitraz or at the 1.0 mg/kg dose of xylazine.
双甲脒是一种用于控制动物体外寄生虫的杀螨剂,具有复杂的药理活性,包括α2-肾上腺素能激动剂作用。本研究的目的是调查双甲脒对马可能产生的镇痛和/或镇静作用。通过头部下垂试验研究了静脉注射二甲基甲酰胺(DMF,5 mL,对照)或双甲脒(0.05、0.10、0.15 mg/kg)的镇静作用。通过静脉注射育亨宾(0.12 mg/kg)研究了α2-肾上腺素能受体在双甲脒引起的镇静作用中的参与情况。为了测量镇痛作用,使用了盐酸赛拉嗪(1 mg/kg,静脉注射,阳性对照)以及相同剂量的双甲脒和DMF。将聚焦的辐射光/热照射到马的球节和肩胛部作为有害刺激,以测量蹄退缩反射潜伏期(HWRL)和皮肤抽搐反射潜伏期(STRL)。所用的三种剂量双甲脒(0.05、0.10和0.15 mg/kg)引起了剂量依赖性的颈部肌肉松弛。双甲脒和赛拉嗪对HWRL的实验表明,静脉注射所有剂量的双甲脒后,注射后长达150分钟HWRL显著增加。此外,在药物注射后长达30分钟,对照(DMF)和阳性对照(赛拉嗪)值之间存在显著差异。另一方面,对STRL的实验表明,在注射0.15 mg/kg剂量的双甲脒后,与对照组相比,STRL显著增加。这种作用在注射后持续长达120分钟。然而,0.05和0.10 mg/kg剂量的双甲脒或1.0 mg/kg剂量的赛拉嗪未观察到显著的镇痛作用。