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非去极化肌松药在其受体部位相互作用的等效线分析

Isobolographic analysis of non-depolarising muscle relaxant interactions at their receptor site.

作者信息

Paul Matthias, Kindler Christoph H, Fokt Ralf M, Dipp Natalie C J, Yost C Spencer

机构信息

Department of Anaesthesia and Perioperative Care, University of California, 513 Parnassus Avenue, Box 0542, San Francisco, CA 94143-0542, USA.

出版信息

Eur J Pharmacol. 2002 Mar 1;438(1-2):35-43. doi: 10.1016/s0014-2999(02)01271-2.

Abstract

Administration of certain combinations of non-depolarising muscle relaxants produces greater than expected neuromuscular blockade. Synergistic effects may be explained by drug interactions with the postsynaptic muscle nicotinic acetylcholine receptor. To investigate this hypothesis, the adult mouse muscle nicotinic acetylcholine receptor (alpha(2)beta delta epsilon) was heterologously expressed in Xenopus laevis oocytes and activated by the application of acetylcholine (10 microM). The effects of five individually applied muscle relaxants and six combinations of structurally similar and dissimilar compounds were studied. Drug combinations containing equipotent concentrations of two agents were tested and dose-response curves were determined. All compounds tested alone and in combination produced rapid and readily reversible, concentration-dependent inhibition. Isobolographic and fractional analyses indicated additive interactions for all six tested combinations. These findings suggest that synergistic neuromuscular blocking effects, observed for the administration of certain combinations of muscle relaxants, do not result from purely postsynaptic binding events at the muscle nicotinic acetylcholine receptor, but rather from differential actions on pre- and postsynaptic sites.

摘要

给予某些非去极化肌松药组合会产生比预期更强的神经肌肉阻滞作用。协同效应可能是由于药物与突触后肌肉烟碱型乙酰胆碱受体相互作用所致。为了研究这一假说,将成年小鼠肌肉烟碱型乙酰胆碱受体(α(2)βδε)在非洲爪蟾卵母细胞中进行异源表达,并通过施加乙酰胆碱(10 μM)来激活。研究了五种单独应用的肌松药以及六种结构相似和不同的化合物组合的作用。测试了含有等效浓度两种药物的组合,并确定了剂量反应曲线。所有单独和联合测试的化合物均产生快速且易于逆转的浓度依赖性抑制作用。等效线图和分数分析表明,所有六种测试组合均存在相加相互作用。这些发现表明,给予某些肌松药组合时观察到的协同神经肌肉阻滞作用并非源于肌肉烟碱型乙酰胆碱受体处纯粹的突触后结合事件,而是源于对突触前和突触后位点的不同作用。

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