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1 the reversible, competitive muscle relaxant, pancuronium.
2 s resistant to alphaCTxGI was antagonized by pancuronium (3-10 microM) and by a 4-oxystilbene derivat
3  general anesthesia (fentanyl, diazepam, and pancuronium) administered by the surgical team.
4                                Gallamine and pancuronium also acted as competitive inhibitors of feta
5  in outside-out patches by (+)-tubocurarine, pancuronium and cisatracurium.
6                                     However, pancuronium and vecuronium each shifted the apparent IC(
7  by sequential administration of thiopental, pancuronium, and potassium chloride.
8 e-Dawley rats were anesthetized and received pancuronium at a rate to completely suppress neuromuscul
9 ect on UA mechanics in a group of paralyzed (pancuronium bromide) rats, despite similar elevations in
10 rmation upon binding of (+)-tubocurarine and pancuronium but not cisatracurium.
11 ergy for association of (+)-tubocurarine and pancuronium compared with cisatracurium is notable.
12                    The same was observed for pancuronium competing with vecuronium.
13                                              Pancuronium did not potentiate the acetylcholine recepto
14 mg protein) and nonstimulated (38.3 +/- 4.8) pancuronium group, as well as the nonstimulated control
15 ion of the tibial nerve after paralysis with pancuronium had no effect on arterial pressure, findings
16 ylamine and eserine; and mixed antagonism by pancuronium, hexamethonium, and d-tubocurarine.
17 ce of acetylcholine) by (+)-tubocurarine and pancuronium on embryonic receptors.
18 acurium did not shift the apparent IC(50) of pancuronium or vecuronium, indicating independent bindin
19  cord hemisected, anesthetized, vagotomized, pancuronium paralyzed, and artificially ventilated male
20 ld greater than that of (+)-tubocurarine and pancuronium, respectively.
21 and 16-fold higher than (+)-tubocurarine and pancuronium, respectively.
22 (-1) for cisatracurium, (+)-tubocurarine and pancuronium, respectively.
23 ents (atracurium, gallamine, metocurine, and pancuronium) to act as competitive antagonists at mouse
24 sion of the reversible competitive inhibitor pancuronium up to 12 hrs does not reduce acetylcholine r
25 (4-36), and 1.5 (0.3-2.9) for cisatracurium, pancuronium, vecuronium, and rocuronium, respectively.
26 ther competitive antagonists: cisatracurium, pancuronium, vecuronium, and rocuronium.