Hsu W H, Lu Z X, Hembrough F B
Toxicol Appl Pharmacol. 1986 Jun 30;84(2):418-22. doi: 10.1016/0041-008x(86)90150-x.
The effect of amitraz on heart rate (HR) and mean aortic blood pressure (MAP) were studied in five conscious male dogs. An iv injection of amitraz (1 mg/kg) caused a decrease in HR, which was accompanied by sinus arrhythmia for at least 60 min. Administration of amitraz also caused an increase in MAP for 20 min. Atropine sulfate (0.045 mg/kg, iv) increased HR and prevented amitraz-induced bradycardia. In addition, atropine potentiated amitraz-induced hypertension for 45 min. Yohimbine, an alpha 2-adrenoreceptor antagonist, given iv at 0.1 mg/kg, prevented hypertension, bradycardia, and sinus arrhythmia induced by amitraz. Tolazoline, a nonselective alpha-adrenoreceptor antagonist, given iv at 5 mg/kg, reduced the bradycardia and sinus arrhythmia caused by amitraz administration but did not change amitraz-induced hypertension. Tolazoline alone also increased both HR and MAP. Prazosin, an alpha 1-adrenoreceptor antagonist, given iv at 1 mg/kg, did not affect the cardiovascular actions of amitraz. The results suggest that (1) alpha 2-adrenoreceptors mediate amitraz-induced bradycardia and hypertension, and (2) yohimbine, but not atropine, can be used to control the untoward reactions of amitraz.
在五只清醒雄性犬中研究了双甲脒对心率(HR)和平均主动脉血压(MAP)的影响。静脉注射双甲脒(1毫克/千克)导致心率下降,并伴有至少60分钟的窦性心律失常。给予双甲脒还导致MAP在20分钟内升高。硫酸阿托品(0.045毫克/千克,静脉注射)使心率增加并预防了双甲脒引起的心动过缓。此外,阿托品使双甲脒引起的高血压增强了45分钟。育亨宾,一种α2肾上腺素能受体拮抗剂,以0.1毫克/千克静脉注射,预防了双甲脒引起的高血压、心动过缓和窦性心律失常。妥拉唑啉,一种非选择性α肾上腺素能受体拮抗剂,以5毫克/千克静脉注射,减轻了双甲脒给药引起的心动过缓和窦性心律失常,但未改变双甲脒引起的高血压。单独使用妥拉唑啉也使HR和MAP均升高。哌唑嗪,一种α1肾上腺素能受体拮抗剂,以1毫克/千克静脉注射,不影响双甲脒的心血管作用。结果表明:(1)α2肾上腺素能受体介导双甲脒引起的心动过缓和高血压;(2)育亨宾而非阿托品可用于控制双甲脒的不良反应。