首页> 美国卫生研究院文献>Journal of the American Association for Laboratory Animal Science : JAALAS >Combining Sevoflurane Anesthesia with Fentanyl–Midazolam or S-Ketamine in Laboratory Mice
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Combining Sevoflurane Anesthesia with Fentanyl–Midazolam or S-Ketamine in Laboratory Mice

机译:七氟醚麻醉与芬太尼-咪达唑仑或S-氯胺酮合用在实验小鼠中

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摘要

Laboratory mice typically are anesthetized by either inhalation of volatile anesthetics or injection of drugs. Here we compared the acute and postanesthetic effects of combining both methods with standard inhalant monoanesthesia using sevoflurane in mice. After injection of fentanyl–midazolam or S-ketamine as premedication, a standard 50-min anesthesia was conducted by using sevoflurane. Addition of fentanyl–midazolam (0.04 mg/kg–4 mg/kg) induced sedation, attenuation of aversive behaviors at induction, shortening of the induction phase, and reduced the sevoflurane concentration required by one third (3.3% compared with 5%), compared with S-ketamine (30 mg/kg) premedication or sevoflurane alone. During anesthesia, heart rate and core body temperature were depressed significantly by both premedications but in general remained within normal ranges. In contrast, with or without premedication, substantial respiratory depression was evident, with a marked decline in respiratory rate accompanied by hypoxia, hypercapnia, and acidosis. Arrhythmia, apnea, and occasionally death occurred under S-ketamine–sevoflurane. Postanesthetic telemetric measurements showed unchanged locomotor activity but elevated heart rate and core body temperature at 12 h; these changes were most prominent during sevoflurane monoanesthesia and least pronounced or absent during fentanyl–midazolam–sevoflurane. In conclusion, combining injectable and inhalant anesthetics in mice can be advantageous compared with inhalation monoanesthesia at induction and postanesthetically. However, adverse physiologic side effects during anesthesia can be exacerbated by premedications, requiring careful selection of drugs and dosages.
机译:通常通过吸入挥发性麻醉剂或注射药物来麻醉实验室小鼠。在这里,我们比较了两种方法与七氟醚在小鼠中与标准吸入性单麻醉联合​​使用的急性和麻醉后效果。注射芬太尼-咪达唑仑或S-氯胺酮作为处方药后,使用七氟醚进行标准的50分钟麻醉。加入芬太尼-咪达唑仑(0.04 mg / kg-4 mg / kg)引起的镇静作用,诱导时厌恶行为的减弱,诱导期的缩短以及所需的七氟醚浓度降低了三分之一(3.3%比5%),与单独服用S-氯胺酮(30 mg / kg)或七氟醚相比。在麻醉期间,两种处方药均显着降低了心率和核心体温,但总体上保持在正常范围内。相比之下,无论有无用药,明显的呼吸抑制都是明显的,呼吸频率明显下降,并伴有缺氧,高碳酸血症和酸中毒。 S-氯胺酮-七氟醚引起心律不齐,呼吸暂停,并偶有死亡。麻醉后的遥测测量显示运动能力未改变,但12 h时心率和核心体温升高。这些变化在七氟醚单麻醉期间最明显,而在芬太尼-咪达唑仑-七氟醚中则最不明显或不存在。总而言之,与诱导和麻醉后吸入单麻醉相比,在小鼠中组合注射麻醉剂和吸入麻醉剂可能是有利的。然而,麻醉期间不良的生理副作用可能会因预先用药而加剧,需要仔细选择药物和剂量。

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