University Laboratory Animal Resources, University of Pennsylvania, Philadelphia, Pennsylvania; University of Pennsylvania School of Veterinary Medicine, Philadelphia, Dept. of Pathobiology, Philadelphia, Pennsylvania.
The Ohio State University College of Veterinary Medicine, Columbus, Ohio.
J Am Assoc Lab Anim Sci. 2021 May 1;60(3):289-297. doi: 10.30802/AALAS-JAALAS-20-000143. Epub 2021 May 10.
Oxygen supplementation is rarely considered when anesthetizing laboratory mice, despite reports that mice become profoundly hypoxic under anesthesia. Little is known about the effects of hypoxia on anesthetic performance. This article focuses on the effects of oxygen supplementation on physiologic parameters and depth of anesthesia in male and female C57BL/6 mice. Anesthesia was performed via common injectable anesthetic protocols and with isoflurane. Mice anesthetized with injectable anesthesia received one of 3 drug protocols. Low-dose ketamine/xylazine (100/8 mg/kg) was chosen to provide immobilization of mice, suitable for imaging procedures. Medium-dose ketamine/xylazine/acepromazine (100/10/1 mg/kg) was chosen as a dose that has been recommended for surgical procedures. High-dose ketamine/xylazine/acepromazine (150/12/3 mg/kg) was chosen after pilot studies to provide a long duration of a deep plane of anesthesia. We also tested the effects of oxygen supplementation on the minimum alveolar concentration (MAC) of isoflurane in mice. Mice breathed supplemental 100% oxygen, room air, or medical air with 21% oxygen. Anesthetized mice that did not receive supplemental oxygen all became hypoxic, while hypoxia was prevented in mice that received oxygen. Oxygen supplementation did not affect the MAC of isoflurane. At the high injectable dose, all mice not receiving oxygen supplementation died while all mice receiving oxygen supplementation survived. At low and medium doses, supplemental oxygen reduced the duration of the surgical plane of anesthesia (low dose with oxygen: 22 ± 14 min; low dose without supplementation: 29 ± 18 min; medium dose with oxygen: 43 ± 18 min; medium dose without supplementation: 61 ± 27 min). These results suggest that mice anesthetized with injectable and inhalant anesthesia without supplemental oxygen are routinely hypoxic. This hypoxia prolongs the duration of anesthesia with injectable drug protocols and affects survival at high doses of injectable anesthetics. Because of variable responses to injectable anesthetics in mice, oxygen supplementation is recommended for all anesthetized mice.
在给实验小鼠麻醉时,很少考虑补充氧气,尽管有报道称小鼠在麻醉下会出现严重缺氧。关于缺氧对麻醉效果的影响知之甚少。本文重点研究了氧补充对雄性和雌性 C57BL/6 小鼠生理参数和麻醉深度的影响。麻醉通过常见的注射麻醉方案和异氟烷进行。接受注射麻醉的小鼠接受了 3 种药物方案之一。选择低剂量的氯胺酮/二甲噻嗪(100/8mg/kg)以提供小鼠的固定,适合成像程序。选择中等剂量的氯胺酮/二甲噻嗪/乙酰丙嗪(100/10/1mg/kg)作为已推荐用于手术程序的剂量。在试点研究后选择高剂量的氯胺酮/二甲噻嗪/乙酰丙嗪(150/12/3mg/kg)以提供深度麻醉的长时间持续时间。我们还测试了氧补充对异氟烷在小鼠中的最低肺泡浓度(MAC)的影响。小鼠呼吸补充的 100%氧气、室内空气或含 21%氧气的医用空气。未接受补充氧气的麻醉小鼠均出现缺氧,而接受氧气的小鼠则防止了缺氧。氧补充不影响异氟烷的 MAC。在高注射剂量下,所有未接受氧补充的小鼠均死亡,而所有接受氧补充的小鼠均存活。在低剂量和中剂量下,补充氧气减少了手术麻醉平面的持续时间(低剂量吸氧:22±14min;低剂量无补充:29±18min;中剂量吸氧:43±18min;中剂量无补充:61±27min)。这些结果表明,未接受补充氧气的注射和吸入麻醉的小鼠常规性缺氧。这种缺氧延长了注射药物方案的麻醉持续时间,并影响高剂量注射麻醉剂的存活。由于小鼠对注射麻醉剂的反应不同,建议所有麻醉的小鼠都进行氧补充。