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在氟烷麻醉的小马中使用新斯的明和依酚氯铵对抗泮库溴铵的神经肌肉阻滞作用。

Antagonism of pancuronium neuromuscular blockade in halothane-anesthetized ponies using neostigmine and edrophonium.

作者信息

Hildebrand S V, Howitt G A

出版信息

Am J Vet Res. 1984 Nov;45(11):2276-80.

PMID:6524720
Abstract

Efficacy of neostigmine (0.04 mg/kg of body weight) and edrophonium (1 mg/kg), as antagonists for pancuronium neuromuscular blockade in halothane-anesthetized ponies, was evaluated. Neostigmine and edrophonium were satisfactory antagonists, with edrophonium having a significantly (P less than 0.01) more rapid onset of action than did neostigmine. Muscarinic activity of neostigmine and edrophonium was also evaluated. Neither antagonist was administered with atropine. Gastrointestinal effects, increased salivation, and increased airway secretions were minimal with edrophonium, but were marked after neostigmine. Blood pressure increased within 1 to 2 minutes of antagonist administration. Heart rate decreased after edrophonium injection, but this occurred after blood pressure increase. Heart rate increased or did not change after neostigmine administration.

摘要

评估了新斯的明(0.04毫克/千克体重)和依酚氯铵(1毫克/千克)作为氟烷麻醉小马泮库溴铵神经肌肉阻滞拮抗剂的效果。新斯的明和依酚氯铵都是满意的拮抗剂,依酚氯铵的起效时间比新斯的明快得多(P小于0.01)。还评估了新斯的明和依酚氯铵的毒蕈碱活性。两种拮抗剂均未与阿托品合用。依酚氯铵引起的胃肠道效应、唾液分泌增加和气道分泌物增加很轻微,但新斯的明给药后这些反应很明显。给药后1至2分钟内血压升高。注射依酚氯铵后心率下降,但这发生在血压升高之后。新斯的明给药后心率增加或未改变。

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