Ko J C, Smith T A, Kuo W C, Nicklin C F
Department of Large Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville 32610-0136, USA.
J Am Anim Hosp Assoc. 1998 Sep-Oct;34(5):407-16. doi: 10.5326/15473317-34-5-407.
Ten ferrets were used in a crossover study to determine the sedative effects of intramuscularly administered diazepam (3 mg/kg body weight)-butorphanol (0.2 mg/kg body weight)-ketamine (15 mg/kg body weight); acepromazine (0.1 mg/kg body weight)-butorphanol (0.2 mg/kg body weight)-ketamine (15 mg/kg body weight); and xylazine (2 mg/kg body weight)-butorphanol (0.2 mg/kg body weight)-ketamine (15 mg/kg body weight). All of the ferrets became laterally recumbent following the administration of each drug combination. The xylazine-butorphanol-ketamine combination induced significantly longer (p less than 0.05) durations of tail-clamp analgesia (mean+/-standard deviation [SD], 81.0+/-19.1 min versus 20.5+/-25.4 min and 30.0+/-26.9 min), dorsal recumbency (mean+/-SD, 94.6+/-13.6 min versus 75. 6+/-34.7 min and 55.2+24.8 min), and muscle relaxation suitable for endotracheal intubation (mean+/-SD, 67.1+/-23.0 min versus 7.0+/-22.1 min and 9.5+/-15.4 min) than the diazepam-butorphanol-ketamine and acepromazine-butorphanol-ketamine combinations, respectively. The recovery time from dorsal recumbency to standing was not significantly different among the three treatment groups. The heart rate was significantly lower in the xylazine-butorphanol-ketamine group; however, systolic blood pressure was not significantly different among the treatment groups. Ventilatory function was more depressed in the diazepam-butorphanol-ketamine and xylazine-butorphanol-ketamine groups than in the acepromazine-butorphanol-ketamine group. A period (approximately 45 minutes) of hypoxia was observed in the xylazine-butorphanol-ketamine-treated ferret. Of the three combinations evaluated in ferrets, xylazine-butorphanol-ketamine was concluded to be the most effective anesthetic combination. However, hypoxemia and ventricular arrhythmias were observed in the xylazine-butorphanol-ketamine-treated ferrets, so the effectiveness of the xylazine-butorphanol-ketamine combination should be weighed against its cardiorespiratory side effects.
在一项交叉研究中,使用了10只雪貂来确定肌肉注射地西泮(3毫克/千克体重)-布托啡诺(0.2毫克/千克体重)-氯胺酮(15毫克/千克体重);乙酰丙嗪(0.1毫克/千克体重)-布托啡诺(0.2毫克/千克体重)-氯胺酮(15毫克/千克体重);以及赛拉嗪(2毫克/千克体重)-布托啡诺(0.2毫克/千克体重)-氯胺酮(15毫克/千克体重)的镇静效果。给予每种药物组合后,所有雪貂均出现侧卧。与地西泮-布托啡诺-氯胺酮组合和乙酰丙嗪-布托啡诺-氯胺酮组合相比,赛拉嗪-布托啡诺-氯胺酮组合诱导的尾夹镇痛持续时间显著更长(p小于0.05)(平均值±标准差[SD],分别为81.0±19.1分钟、20.5±25.4分钟和30.0±26.9分钟),背卧位持续时间(平均值±标准差,分别为94.6±13.6分钟、75.6±34.7分钟和55.2±24.8分钟),以及适合气管插管的肌肉松弛持续时间(平均值±标准差,分别为67.1±23.0分钟、7.0±22.1分钟和9.5±15.4分钟)。三个治疗组从背卧位恢复到站立的时间没有显著差异。赛拉嗪-布托啡诺-氯胺酮组的心率显著更低;然而,治疗组之间的收缩压没有显著差异。地西泮-布托啡诺-氯胺酮组和赛拉嗪-布托啡诺-氯胺酮组的通气功能比乙酰丙嗪-布托啡诺-氯胺酮组更受抑制。在接受赛拉嗪-布托啡诺-氯胺酮治疗的雪貂中观察到一段(约45分钟)缺氧期。在雪貂中评估的三种组合中,赛拉嗪-布托啡诺-氯胺酮被认为是最有效的麻醉组合。然而,在接受赛拉嗪-布托啡诺-氯胺酮治疗的雪貂中观察到低氧血症和室性心律失常,因此赛拉嗪-布托啡诺-氯胺酮组合的有效性应与其心肺副作用相权衡。