ライフサイエンスコーパス: pancuronium

コーパス検索結果 (１語後でソート)

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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 ylamine and eserine; and mixed antagonism by pancuronium, hexamethonium, and d-tubocurarine.

16 ce of acetylcholine) by (+)-tubocurarine and pancuronium on embryonic receptors.

17 acurium did not shift the apparent IC(50) of pancuronium or vecuronium, indicating independent bindin

18 cord hemisected, anesthetized, vagotomized, pancuronium paralyzed, and artificially ventilated male

19 ld greater than that of (+)-tubocurarine and pancuronium, respectively.

20 and 16-fold higher than (+)-tubocurarine and pancuronium, respectively.

21 (-1) for cisatracurium, (+)-tubocurarine and pancuronium, respectively.

22 ents (atracurium, gallamine, metocurine, and pancuronium) to act as competitive antagonists at mouse

23 sion of the reversible competitive inhibitor pancuronium up to 12 hrs does not reduce acetylcholine r

24 (4-36), and 1.5 (0.3-2.9) for cisatracurium, pancuronium, vecuronium, and rocuronium, respectively.

25 ther competitive antagonists: cisatracurium, pancuronium, vecuronium, and rocuronium.

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