Tuval Avishag, Las Liora, Shilo-Benjamini Yael
1 Department of Veterinary Resources, Weizmann Institute of Science, Israel.
2 Department of Neurobiology, Weizmann Institute of Science, Israel.
Lab Anim. 2018 Oct;52(5):515-525. doi: 10.1177/0023677218756456. Epub 2018 Feb 15.
Egyptian fruit bats are increasingly used as model animals in neuroscience research. Our aim was to characterize suitable injectable anaesthesia for this species, possibly replacing inhalant anaesthesia, thus minimizing occupational health hazards. Eight bats were randomly assigned by a crossover design for subcutaneously administered combinations of medetomidine-midazolam with: saline (MM-Sal), ketamine (MM-Ket), fentanyl (MM-Fen), morphine (MM-Mor), or butorphanol (MM-But). The anaesthetic depth and vital signs were monitored at baseline and every 10 min until bats recovered. If after 180 min the bats did not recover, atipamezole was administered. Mean induction times were 7-11.5 min with all combinations. Twitching during induction was common. All combinations produced anaesthesia, with significantly decreased heart rate (from 400 to 200 bpm) and respiratory rate (from 120-140 to 36-65 rpm). Arrhythmia and irregular breathing patterns occurred. MM-Fen, MM-Mor, and MM-But depressed respiration significantly more than MM-Sal. Time to first movement with MM-Ket and MM-But lasted significantly longer than with MM-Sal. Recovery time was significantly shorter in the MM-Sal (88 min) in comparison to all other treatments, and it was significantly longer in the MM-But (159 min), with atipamezole administered to four of the eight bats. In conclusion, all five anaesthetic protocols are suitable for Egyptian fruit bats; MM-Ket produces long anaesthesia and minimal respiratory depression, but cannot be antagonized completely. MM-Fen, MM-Mor, and MM-But depress respiration, but are known to produce good analgesia, and can be fully antagonized. Administration of atipamezole following the use of MM-But in Egyptian fruit bats is recommended.
埃及果蝠越来越多地被用作神经科学研究的模式动物。我们的目的是确定适合该物种的可注射麻醉剂,以可能取代吸入麻醉,从而将职业健康风险降至最低。八只蝙蝠通过交叉设计被随机分配,皮下注射美托咪定 - 咪达唑仑与以下药物的组合:生理盐水(MM - Sal)、氯胺酮(MM - Ket)、芬太尼(MM - Fen)、吗啡(MM - Mor)或布托啡诺(MM - But)。在基线时以及每隔10分钟监测一次麻醉深度和生命体征,直至蝙蝠恢复。如果180分钟后蝙蝠仍未恢复,则给予阿替美唑。所有组合的平均诱导时间为7 - 11.5分钟。诱导期间抽搐很常见。所有组合均产生麻醉效果,心率(从400次/分钟降至200次/分钟)和呼吸频率(从120 - 140次/分钟降至36 - 65次/分钟)显著降低。出现了心律失常和不规则呼吸模式。MM - Fen、MM - Mor和MM - But对呼吸的抑制明显大于MM - Sal。使用MM - Ket和MM - But后首次活动的时间明显长于MM - Sal。与所有其他治疗相比,MM - Sal组的恢复时间明显更短(88分钟),而MM - But组明显更长(159分钟),八只蝙蝠中有四只使用了阿替美唑。总之,所有五种麻醉方案都适用于埃及果蝠;MM - Ket产生长时间麻醉且呼吸抑制最小,但不能完全拮抗。MM - Fen、MM - Mor和MM - But抑制呼吸,但已知具有良好的镇痛作用,并且可以完全拮抗。建议在埃及果蝠使用MM - But后给予阿替美唑。