Smith Briony D, Vail Krystal J, Carroll Gwendolyn L, Taylor Maggie C, Jeffery Nicholas D, Vemulapalli Tracy H, Elliott James J
Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, Texas;, Email:
Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, Texas.
J Am Assoc Lab Anim Sci. 2018 Mar 1;57(2):202-209.
Often few alternative anesthetics for exotic species are available, due to the small numbers of these animals used in research. In this study, we evaluated the depth and duration of anesthesia in Xenopus laevis after their immersion in 3 doses of etomidate (15, 22.5, and 30 mg/L) and in 3 doses of benzocaine (0.1%, 0.5%, and 1%) compared with the 'gold standard,' tricaine methanesulfonate (MS222; 2 g/L). We then chose an optimal dose for each alternative anesthetic according to induction time, duration of surgical plane, and time to complete recovery. The optimal etomidate and benzocaine doses (22.5 mg/L and 0.1%, respectively) as well as the MS222 dose were then used to achieve a surgical plane of anesthesia, with the addition of flunixin meglumine (25 or 50 mg/kg) administered in the dorsal lymph sac at the completion of mock oocyte harvest. Efficacy of the analgesic was assessed at 1, 3, 6, and 24 h postoperatively by using acetic acid testing (AAT). Histology of the liver, kidney, and tissues surrounding the dorsal lymph sac was performed at day 3, 14, and 28 in each group of animals. Mild to moderate myocyte degeneration and necrosis were present in tissues surrounding the dorsal lymph sac at both flunixin meglumine doses after etomidate and benzocaine anesthesia. In addition, the 50-mg/kg dose of flunixin meglumine resulted in the death of 5 of the 12 frogs within 24 h, despite an otherwise uneventful anesthetic recovery. In conclusion, benzocaine and etomidate offer alternative anesthetic regimens, according to typical requirements for an anesthetic event. Flunixin meglumine at the 25-mg/kg dose provided analgesic relief at the latest time point during etomidate dosage and at all time points during benzocaine dosage, but further characterization is warranted regarding long-term or repeated analgesic administration.
由于用于研究的这些动物数量较少,通常很少有适合外来物种的替代麻醉剂。在本研究中,我们评估了非洲爪蟾浸入3种剂量的依托咪酯(15、22.5和30 mg/L)和3种剂量的苯佐卡因(0.1%、0.5%和1%)后的麻醉深度和持续时间,并与“金标准”甲磺酸三卡因(MS222;2 g/L)进行比较。然后,我们根据诱导时间、手术平面持续时间和完全恢复时间,为每种替代麻醉剂选择了最佳剂量。然后使用最佳剂量的依托咪酯和苯佐卡因(分别为22.5 mg/L和0.1%)以及MS222剂量来达到麻醉手术平面,并在模拟采卵结束时在背淋巴囊注射氟尼辛葡甲胺(25或50 mg/kg)。术后1、3、6和24小时通过醋酸试验(AAT)评估镇痛效果。在每组动物的第3、14和28天对肝脏、肾脏和背淋巴囊周围组织进行组织学检查。依托咪酯和苯佐卡因麻醉后,两种氟尼辛葡甲胺剂量下背淋巴囊周围组织均出现轻度至中度的心肌细胞变性和坏死。此外,尽管麻醉恢复过程顺利,但50 mg/kg剂量的氟尼辛葡甲胺导致12只青蛙中有5只在24小时内死亡。总之,根据麻醉事件的典型要求,苯佐卡因和依托咪酯提供了替代麻醉方案。25 mg/kg剂量的氟尼辛葡甲胺在依托咪酯给药的最晚时间点以及苯佐卡因给药的所有时间点均提供了镇痛效果,但对于长期或重复镇痛给药,仍需要进一步研究。