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Antagonism of pancuronium and its metabolites by neostigmine in cats.

作者信息

Booij L H, Miller R D, Jones M J, Stanski D R

出版信息

Anesth Analg. 1979 Nov-Dec;58(6):483-6. doi: 10.1213/00000539-197911000-00008.

DOI:10.1213/00000539-197911000-00008
PMID:574733
Abstract

Antagonism by neostigmine of neuromuscular blockade produced by pancuronium or its metabolites was studied in the cat anterior or tibialis muscle-peroneal nerve preparation using constant infusions of muscle relaxants. The ED50 of neostigmine (dose which caused a 50% antagonism) was 16, 11, 29, and 26 micrograms/kg for pancuronium, 3-hydroxypancuronium, 17-hydroxypancuronium, and 3, 17-hydroxypancuronium, respectively. Times of onset of neostigmine action were shorter when antagonizing 17-hydroxypancuronium neuromuscular blockade. Duration of neostigmine action when antagonizing 17- or 3, 17-hydroxypancuronium blockade was shorter than with pancuronium or 3-hydroxypancuronium. We conclude that more neostigmine is required to antagonize 17- or 3,17-hydroxypancuronium neuromuscular blockade than is required to antagonize pancuronium. Conversely, less neostigmine was required to antagonize 3-hydroxypancuronium blockade.

摘要

相似文献

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引用本文的文献

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Neuromuscular transmission and its pharmacological blockade. Part 3: Continuous infusion of relaxants and reversal and monitoring of relaxation.神经肌肉传递及其药理学阻断。第3部分:肌肉松弛剂的持续输注以及松弛作用的逆转与监测。
Pharm World Sci. 1997 Feb;19(1):35-44. doi: 10.1023/a:1008645511543.
2
Org-NC45: a new steroidal non-depolarizing muscle relaxant.
Pharm Weekbl Sci. 1982 Feb 19;4(1):1-4. doi: 10.1007/BF02112349.