Fox Lana, Mans Christoph
Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin;, Email:
J Am Assoc Lab Anim Sci. 2018 May 1;57(3):286-290. doi: 10.30802/AALAS-JAALAS-17-000108. Epub 2018 Apr 24.
Buprenorphine is routinely used in chinchillas at reported doses of 0.01 to 0.1 mg/kg IM or SC. However, these dose recommendations are based on anecdotal reports or extrapolation from studies in other species. Therefore, the purpose of this study was to evaluate the analgesic efficacy and safety of subcutaneously administered buprenorphine in chinchillas. Using a randomized, blind, controlled, complete crossover design, we evaluated buprenorphine at a single dose of 0.05, 0.1 or 0.2 mg/kg SC (experiment A) and 0.2 mg/kg SC (experiment B). Analgesic efficacy was determined by measuring limb withdrawal latencies in response to a thermal noxious stimulus (Hargreaves method) at 0, 3, 6, 12, and 24 h (experiment A) and at 0, 1, 2, 4, and 8 h (experiment B). In a third experiment, food intake and fecal output were monitored after repeated administration of buprenorphine (0.2 mg/kg SC every 6 h for 3 doses). Buprenorphine at 0.2 mg/kg SC, but not at 0.05 or 0.1 mg/kg SC, significantly increased limb withdrawal latencies for less than 4 h. Self-limiting reduction in food intake and fecal output occurred after administration at the 0.2-mg/kg dose in animals undergoing algesiometry. In chinchillas not undergoing algesiometry, the administration of 3 doses at 0.2 mg/kg SC every 6 h did not reduce food intake but significantly decreased fecal output for the first 24 h. Additional studies are needed to evaluate buprenorphine in different algesiometry models and to establish its pharmacokinetic profile in chinchillas.
丁丙诺啡通常以0.01至0.1毫克/千克的剂量肌肉注射或皮下注射用于龙猫。然而,这些剂量建议是基于轶事报告或从其他物种的研究推断而来。因此,本研究的目的是评估皮下注射丁丙诺啡对龙猫的镇痛效果和安全性。我们采用随机、盲法、对照、完全交叉设计,评估了单剂量0.05、0.1或0.2毫克/千克皮下注射丁丙诺啡(实验A)和0.2毫克/千克皮下注射丁丙诺啡(实验B)的情况。通过在0、3、6、12和24小时(实验A)以及0、1、2、4和8小时(实验B)测量对热伤害性刺激的肢体退缩潜伏期(哈格里夫斯方法)来确定镇痛效果。在第三个实验中,在重复给予丁丙诺啡(每6小时皮下注射0.2毫克/千克,共3剂)后监测食物摄入量和粪便排出量。0.2毫克/千克皮下注射的丁丙诺啡,但不是0.05或0.1毫克/千克皮下注射的丁丙诺啡,显著增加了肢体退缩潜伏期,持续时间不到4小时。在进行痛觉测量的动物中,以0.2毫克/千克剂量给药后,食物摄入量和粪便排出量出现自限性减少。在未进行痛觉测量的龙猫中,每6小时皮下注射0.2毫克/千克共3剂,在前24小时内没有减少食物摄入量,但显著减少了粪便排出量。需要进一步的研究来评估丁丙诺啡在不同痛觉测量模型中的效果,并确定其在龙猫中的药代动力学特征。