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阿替美唑和氟马西尼对美托咪定-咪达唑仑诱导的实验猪镇静作用的拮抗效应。

Antagonistic effects of atipamezole and flumazenil on medetomidine-midazolam induced sedation in laboratory pigs.

作者信息

Nishimura R, Kim H, Matsunaga S, Hayashi K, Sasaki N, Tamura H, Takeuchi A

机构信息

Department of Veterinary Surgery, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

J Vet Med Sci. 1993 Oct;55(5):789-93. doi: 10.1292/jvms.55.789.

Abstract

Antagonistic effects of atipamezole (80, 160 and 240 micrograms/kg, im), and flumazenil (100 micrograms/kg, iv) or atipamezole (80 micrograms/kg) and flumazenil (100 micrograms/kg) on medetomidine-midazolam induced sedation were evaluated in laboratory pigs. Atipamezole at each dose effectively reversed sedation, and the arousal time, standing time and total recovery time were significantly shortened. The optimal action of atipamezole was seen at a dose of 160 micrograms/kg. At this dose recovery from the sedation was quick and smooth, and adverse effects such as hyperactivity or tachycardia were minimal. Flumazenil reversed sedation temporary, but the pigs went back to moderate sedation soon after arousal. The combination of atipamezole and flumazenil most effectively reversed the sedation, however atipamezole (160 micrograms/kg) alone was thought to be practically potent enough to antagonize sedation induced by medetomidine-midazolam in laboratory pigs.

摘要

在实验猪中评估了阿替美唑(80、160和240微克/千克,肌肉注射)、氟马西尼(100微克/千克,静脉注射)或阿替美唑(80微克/千克)与氟马西尼(100微克/千克)对美托咪定-咪达唑仑诱导的镇静作用的拮抗效果。各剂量的阿替美唑均能有效逆转镇静作用,且苏醒时间、站立时间和总恢复时间均显著缩短。阿替美唑在160微克/千克剂量时作用最佳。在此剂量下,从镇静状态恢复迅速且平稳,多动或心动过速等不良反应最小。氟马西尼可暂时逆转镇静作用,但猪在苏醒后很快又恢复到中度镇静状态。阿替美唑与氟马西尼联合使用最有效地逆转了镇静作用,然而,单独使用阿替美唑(160微克/千克)被认为在实际应用中足以有效拮抗实验猪中美托咪定-咪达唑仑诱导的镇静作用。

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