MD-PhD Program, School of Medicine, Wayne State University, Detroit, Michigan; Department of Biomedical Engineering, Wayne State University, Detroit, Michigan; School of Medicine, Wayne State University, Detroit, Michigan;, Email:
Division of Laboratory Animal Resources, Wayne State University, Detroit, Michigan.
J Am Assoc Lab Anim Sci. 2020 Mar 1;59(2):186-196. doi: 10.30802/AALAS-JAALAS-19-000063. Epub 2020 Jan 21.
Effective pain relief in animals relies on the ability to discern pain and assess its severity. However, few objective measures exist to assess the presence and severity of pain in axolotls, and few resources are available regarding drugs and appropriate doses to provide pain relief in this species. This study evaluated behavioral tools for cageside pain assessment and validated a reproducible and reliable quantitative method to evaluate analgesic efficacy in axolotls. Animals were divided into control and treatment groups ( = 6 per group); treatment groups received buprenorphine through injection (50 mg/kg every 24 h for 48 h intracelomically) or butorphanol immersion (0.50 or 0.75 mg/L every 24 h for 48 h). Qualitative behavioral tests, adapted from other amphibian studies, included tapping on the home tank, directing water jets or physically touching specific anatomic points on the animal, and placing a novel object in the home tank. Quantitative methods used to produce noxious stimuli were the acetic acid test and von Frey aesthesiometers. Animals that were treated with analgesics did not demonstrate a significant difference compared with controls during behavioral assessment at 1, 6, 12, 25, 30, and 48 h after analgesia administration. The acetic acid test revealed a reproducible, concentration-dependent pain response. However, a significant difference in the AAT response was not observed between control and treated groups with the tested analgesics and doses.
动物的有效止痛依赖于辨别疼痛和评估其严重程度的能力。然而,很少有客观的方法来评估蝾螈的疼痛存在和严重程度,而且关于这种物种的药物和适当剂量的止痛资源也很少。本研究评估了用于笼边疼痛评估的行为工具,并验证了一种可重复和可靠的定量方法来评估蝾螈的镇痛效果。动物被分为对照组和治疗组(每组 6 只);治疗组通过注射(24 小时内每 50 毫克/千克,共 48 小时)或丁丙诺啡浸泡(24 小时内每 0.50 或 0.75 毫克/升,共 48 小时)接受丁丙诺啡。从其他两栖动物研究中改编的定性行为测试包括敲击家箱、引导水流或物理触摸动物的特定解剖点,以及在家箱中放置新物体。用于产生有害刺激的定量方法是醋酸试验和冯弗雷触觉计。与对照组相比,接受镇痛治疗的动物在镇痛后 1、6、12、25、30 和 48 小时的行为评估中没有表现出明显的差异。醋酸试验显示出可重复的、浓度依赖性的疼痛反应。然而,在测试的镇痛剂和剂量下,对照组和治疗组之间的 AAT 反应没有观察到显著差异。