University Laboratory Animal Resources, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Comparative Medicine, Stanford University School of Medicine, Stanford, California.
J Am Assoc Lab Anim Sci. 2022 Sep 1;61(5):457-467. doi: 10.30802/AALAS-JAALAS-21-000125. Epub 2022 Aug 8.
Balanced anesthesia-the use of a combination of drugs to achieve a desired anesthetic plane-offers many benefits, including smoother induction and recovery and fewer adverse effects than occur with individual drugs. Although premedication prior to inhalant anesthesia is routine in other species, mice are commonly induced with gas anesthesia alone. The hypothesis of this study was that premedication with ketamine or xylazine would safely reduce the stress of isoflurane induction and lower the minimum alveolar concentration (MAC) of isoflurane. Young adult male and female C57BL/6J mice were premedicated with ketamine (100 mg/kg), xylazine (4 mg/kg), or isotonic crystalloid (0.1 mL) and were used in 4 experiments. First, isoflurane induction was video recorded under all test conditions, and the videos were scored according to a behavioral ethogram to identify signs of distress. Mice in the ketamine group experienced tremors and ataxia before and dur- ing induction. Therefore, ketamine was given after induction with isoflurane in subsequent experiments. Second, the MAC value for each anesthetic protocol was determined by using quantal and bracketing analysis. Third, mice were anesthetized according to the 3 protocols, and vital parameters were monitored for 60 min. Finally, anesthetized mice were challenged with hypoxia and hypovolemia, and vital parameters were monitored. Premedication with xylazine significantly reduced the stress scores for isoflurane induction (control, 7.3 ± 1.5; ketamine, 6.0 ± 3.0; xylazine, 3.1 ± 1.0). Ketamine and xylazine both reduced the MAC of isoflurane (control, 1.89%; ketamine, 0.96%; xylazine, 1.20%). All mice survived 60 min of anesthesia and the hypoxia-hypovolemia challenge. Premedication with xylazine reduced the stress of induction and lowered the necessary dose of isoflurane in C57BL/6J mice to maintain a surgical plane of anesthesia. We recommend administering xylazine before isoflurane induction and anesthesia of healthy mice that are undergoing procedures in which 100% oxygen is provided and anticipated blood loss is less than 10% to 15% of the total blood volume.
平衡麻醉——使用药物组合来达到所需的麻醉平面——具有许多优点,包括诱导和恢复更平稳,以及与单独使用药物相比,不良反应更少。尽管在其他物种中,吸入麻醉前进行预给药是常规做法,但通常单独使用气体麻醉来诱导小鼠。本研究的假设是,氯胺酮或甲苯噻嗪预给药可以安全地减轻异氟烷诱导的应激反应,并降低异氟烷的最低肺泡浓度(MAC)。年轻成年雄性和雌性 C57BL/6J 小鼠分别用氯胺酮(100mg/kg)、甲苯噻嗪(4mg/kg)或等渗晶体(0.1mL)进行预给药,并在 4 项实验中使用。首先,在所有测试条件下对异氟烷诱导进行视频记录,并根据行为行为表对视频进行评分,以确定痛苦的迹象。氯胺酮组的小鼠在诱导前和诱导期间出现震颤和共济失调。因此,在随后的实验中,在使用异氟烷进行诱导后给予氯胺酮。其次,通过定量和区间分析确定每种麻醉方案的 MAC 值。第三,根据 3 种方案对小鼠进行麻醉,并监测 60 分钟的生命体征。最后,用缺氧和低血容量对麻醉后的小鼠进行挑战,并监测生命体征。甲苯噻嗪预给药显著降低了异氟烷诱导的应激评分(对照组,7.3±1.5;氯胺酮组,6.0±3.0;甲苯噻嗪组,3.1±1.0)。氯胺酮和甲苯噻嗪均降低了异氟烷的 MAC(对照组,1.89%;氯胺酮,0.96%;甲苯噻嗪,1.20%)。所有小鼠均在 60 分钟麻醉和缺氧低血容量挑战中存活。甲苯噻嗪预给药降低了诱导的应激反应,并降低了 C57BL/6J 小鼠维持手术麻醉平面所需的异氟烷剂量。我们建议在 100%氧气供应和预计失血量小于总血量的 10%至 15%的情况下,对接受手术的健康小鼠进行异氟烷诱导和麻醉前使用甲苯噻嗪。