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新斯的明而非依酚氯铵可延长米库氯铵的作用时间。

Neostigmine but not edrophonium prolongs the action of mivacurium.

作者信息

Symington M J, Mirakhur R K, Kumar N

机构信息

Department of Anaesthetics, Queen's University of Belfast, N Ireland, UK.

出版信息

Can J Anaesth. 1996 Dec;43(12):1220-3. doi: 10.1007/BF03013428.

DOI:10.1007/BF03013428
PMID:8955970
Abstract

PURPOSE

To examine the influence of anticholinesterase drugs neostigmine and edrophonium (which have different effects on plasma cholinesterase activity) administered for antagonism of neuromuscular block on the duration of action of mivacurium (a neuromuscular blocking drug metabolised by plasma cholinesterase).

METHODS

This was a randomized study where mivacurium 0.15 mg.kg-1 was administered to a control group or after administration of neostigmine 40 micrograms.kg-1 or edrophonium 1 mg.kg-1 (n = 10 for each group) administered 10 min earlier for antagonism of atracurium-induced neuromuscular block. Neuromuscular block was measured by stimulation of the ulnar nerve in a train-of-four mode (TOF) and measuring the force of contraction of the adductor pollicis muscle. Baseline plasma cholinesterase activity was estimated before drug administration in all the groups and following anticholinesterase administration.

RESULTS

The times to recovery of T1 (first response in the TOF) to 25 and 90% of control and of the TOF ratio to 0.7 after 0.15 mg.kg-1 of mivacurium were 47, 65 and 70 min in the neostigmine group; 25, 36 and 36 min in the edrophonium group and 17, 29 and 27 min respectively in the control group (P < 0.01). The plasma cholinesterase activity (PCHE) after neostigmine decreased from 6596 to 1959 U.L-1 (P < 0.001) but there was no change after edrophonium (6140 to 6396 U.L-1).

CONCLUSIONS

The duration of action of mivacurium is prolonged by previous administration of neostigmine and this is most likely to be due to inhibition of PCHE activity.

摘要

目的

研究用于拮抗神经肌肉阻滞的抗胆碱酯酶药物新斯的明和依酚氯铵(它们对血浆胆碱酯酶活性有不同影响)对米库氯铵(一种由血浆胆碱酯酶代谢的神经肌肉阻滞药物)作用持续时间的影响。

方法

这是一项随机研究,给对照组或在提前10分钟给予40微克/千克新斯的明或1毫克/千克依酚氯铵(每组n = 10)以拮抗阿曲库铵诱导的神经肌肉阻滞后,给予0.15毫克/千克的米库氯铵。通过在四个成串刺激模式(TOF)下刺激尺神经并测量拇收肌的收缩力来测量神经肌肉阻滞。在所有组给药前以及给予抗胆碱酯酶药物后估计基线血浆胆碱酯酶活性。

结果

给予0.15毫克/千克米库氯铵后,新斯的明组T1(TOF中的首次反应)恢复到对照的25%和90%以及TOF比值恢复到0.7的时间分别为47、65和70分钟;依酚氯铵组为25、36和36分钟,对照组分别为17、29和27分钟(P < 0.01)。新斯的明给药后血浆胆碱酯酶活性(PCHE)从6596降至1959 U/L(P < 0.001),但依酚氯铵给药后无变化(6140至6396 U/L)。

结论

预先给予新斯的明会延长米库氯铵的作用持续时间,这很可能是由于抑制了PCHE活性。

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