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Effect of midazolam and butorphanol premedication on inhalant isofluraneanesthesia in mice

机译:咪达唑仑和布托啡诺处方对吸入异氟醚的影响小鼠麻醉

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摘要

Isoflurane is a representative inhalant anesthesia used in laboratory animals. However, isoflurane mediates respiratory depression and adverse clinical reactions during induction. In the present study, we established a novel balanced anesthesia method in mice that combined isoflurane anesthesia with midazolam and butorphanol (MB). Thirty-four male C57BL/6J mice received either isoflurane alone or isoflurane with an intra-peritoneal MB premedication (3 mg/kg midazolam and 4 mg/kg butorphanol). The minimum alveolar concentration (MAC) in each group was evaluated. Induction time and adverse clinical reactions were recorded in each group. Core body temperature, heart rate, respiratory rate, and oxygen saturation (SPO2) were assessed before and for 1 h after induction. Premedication with MB achieved a significant reduction in MAC compared with isoflurane monoanesthesia (isoflurane, 1.38 ± 0.15%; isoflurane with MB, 0.78 ± 0.10%; P<0.05). Induction time was significantly shortened with MB premedication, and adverse reactions such as excitement or incontinence were observed less frequently. Furthermore, isoflurane anesthesia with MB premedication caused increase of respiratory rates compared to isoflurane monoanesthesia. No significant decrease of SPO2 was observed in MBI anesthesia, while a decrease in SPO2 was apparent with isoflurane monoanesthesia (baseline, 98.3% ± 1.1; 10 min after induction,91.8 ± 6.4%; P<0.05). In conclusion, premedication with MB waseffective for the mitigation of respiratory depression induced by isoflurane in mice, withrapid induction and fewer adverse clinical reactions.
机译:异氟醚是用于实验动物的代表性吸入麻醉剂。但是,异氟烷在诱导过程中会介导呼吸抑制和不良临床反应。在本研究中,我们建立了一种新的平衡麻醉方法,该方法将异氟烷麻醉与咪达唑仑和布托啡诺(MB)结合使用。三十四只C57BL / 6J雄性小鼠单独接受异氟烷或异氟烷联合腹膜内用药(3 mg / kg咪达唑仑和4 mg / kg丁烷醇)。评估每组的最低肺泡浓度(MAC)。每组记录诱导时间和不良临床反应。在诱导之前和之后1小时评估核心体温,心率,呼吸频率和氧饱和度(SPO2)。与异氟烷单麻醉相比,MB的预用药可使MAC显着减少(异氟烷1.38±0.15%; MB的异氟烷0.78±0.10%; P <0.05)。 MB预防性用药可大大缩短诱导时间,而较少观察到不良反应,如兴奋或失禁。此外,与异氟烷单麻醉相比,MB预处理的异氟烷麻醉引起呼吸频率增加。在MBI麻醉中未观察到SPO2的显着降低,而异氟烷单麻醉后SPO2的降低明显(基线,98.3%±1.1;诱导后10分钟,91.8±6.4%; P <0.05)。总之,MB的前药治疗是有效减轻异氟烷引起的小鼠呼吸抑制,快速诱导,减少不良临床反应。

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