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[酸碱变化与肌肉松弛剂]

[Acid base changes and muscle relaxants].

作者信息

Ono K, Ohta Y, Nagano O, Aziz L, Hirakawa M

机构信息

Department of Anesthesiology, Fukuyama Municipal Hospital.

出版信息

Masui. 1996 Jan;45(1):2-14.

PMID:8865718
Abstract

Previous publications have provided conflicting results concerning the effects of respiratory and metabolic acid base changes on the neuromuscular effects of nondepolarizing muscle relaxants. The varying results can be attributed not only to experimental design or species difference, but also to the accompanying changes in the pharmacokinetics in vivo. Using the phrenic nerve-hemidiaphragm preparation of rats, in which many variables of in vivo studies can be eliminated, respiratory and metabolic acid-base changes were induced by varying carbon dioxide (PCO2) and bicarbonate (HCO3) concentrations in the Krebs' solution and their effects on the potencies of muscle relaxants were compared. Decreasing pH by increasing Pco2 or by decreasing HCO3 increased the potencies of the monoquaternary relaxants (d-tubocurarine, vecuronium and rocuronium), while pH changes did not affect the potencies of the bisquaternary relaxants (metocurine, pancuronium and pipecuronium). Above difference between mono- and bisquaternary relaxants may reflect pH-induced changes in the ionization of the tertiary ammonium and resulting in changes in the sensitivity to the anionic nicotinic receptors. Neostigmine-induced antagonism was not affected by acid-base changes. These results in vitro were compared and correlated with the previous results in vivo.

摘要

先前的出版物就呼吸和代谢性酸碱变化对非去极化肌松药神经肌肉效应的影响给出了相互矛盾的结果。结果各异不仅可归因于实验设计或物种差异,还可归因于体内药代动力学的伴随变化。利用大鼠膈神经 - 半膈肌标本,该标本可消除体内研究的许多变量,通过改变 Krebs 溶液中的二氧化碳(PCO2)和碳酸氢盐(HCO3)浓度诱导呼吸和代谢性酸碱变化,并比较它们对肌松药效能的影响。通过增加 Pco2 或降低 HCO3 来降低 pH 值会增加单季铵类肌松药(d - 筒箭毒碱、维库溴铵和罗库溴铵)的效能,而 pH 变化不影响双季铵类肌松药(美索卡明、泮库溴铵和哌库溴铵)的效能。单季铵类和双季铵类肌松药之间的上述差异可能反映了 pH 诱导的叔铵离子化变化,并导致对阴离子型烟碱受体的敏感性改变。新斯的明诱导的拮抗作用不受酸碱变化影响。将这些体外实验结果与先前的体内实验结果进行了比较和关联。

相似文献

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The influence of respiratory-induced acid-base changes on the action of non-depolarizing muscle relaxants in rats.
Anesthesiology. 1988 Mar;68(3):357-62. doi: 10.1097/00000542-198803000-00006.

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