阿替帕美唑对马解毒脒镇静作用的拮抗作用

B. Ramseyer, N. Schmucker, U. Schatzmann, A. Busato, Y. Moens
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引用次数: 26

摘要

在6匹马身上研究了iv阿替帕美唑逆转脱毒脒诱导的镇静作用。所有马均静脉注射10μg和20μg/kg bwt脱毒脒,15分钟后再静脉注射6倍、8倍和10倍剂量的阿替帕美唑。阿替美唑引起所有马的快速觉醒,副作用很小。在15分钟观察期结束时,即使使用最高剂量的阿替帕美唑,也没有完全消除由迪托咪定引起的心动过缓、节律紊乱和上睑下垂。所有的马都保持了轻微的镇静,但没有共济失调。在不同剂量的阿替帕美唑和任何剂量的脱毒脒之间,头部高度、心率和镇静评分没有显著差异。根据镇静程度,100μg至160μg/kg bwt阿替帕美唑的剂量足以对抗脱毒脒诱导的马镇静作用。
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Antagonism of detomidine sedation with atipamezole in horses

The reversal of detomidine-induced sedation with iv atipamezole was studied in 6 horses. All horses were injected iv with 10 μg and 20 μg/kg bwt detomidine and 15 min later this was followed by 6-, 8- and 10-fold doses of iv atipamezole. Atipamezole caused a quick arousal in all horses with minor side effects. Bradycardia, rhythm disturbances and head ptosis caused by detomidine were not abolished completely at the end of the 15 min observation period, even with the highest atipamezole doses. All horses remained slightly sedated but without ataxia. There were no significant differences in head height, heart rate and sedation score between the different doses of atipamezole for either dose of detomidine. According to the degree of sedation, doses of 100 μg to 160 μg/kg bwt atipamezole are adequate to antagonise detomidine-induced sedation in the horse.

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