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布比卡因对甲哌卡因蛋白结合的影响。

Influence of bupivacaine on mepivacaine protein binding.

作者信息

Hartrick C T, Dirkes W E, Coyle D E, Raj P P, Denson D D

出版信息

Clin Pharmacol Ther. 1984 Oct;36(4):546-50. doi: 10.1038/clpt.1984.217.

Abstract

To elucidate the mechanism of any drug displacement interaction, we examined the protein binding of mixtures of mepivacaine and bupivacaine in serum and solutions of albumin or alpha 1-acid glycoprotein. Protein binding data with mepivacaine alone were best described by a model with one class of binding site and a partitioning constant in serum and by a model with one class of binding site in both isolated protein solutions. Binding affinity of mepivacaine in serum was reduced in the presence of bupivacaine. Displacement of mepivacaine by bupivacaine was observed when an alpha 1-acid glycoprotein solution was studied. Classic competitive inhibition was demonstrated. Bupivacaine reduced mepivacaine binding to albumin, but the degree of displacement was not significant. When administered simultaneously, these two amino-amide local anesthetics interact synergistically to produce a higher than expected free concentration of mepivacaine. This interaction increases the risk of toxicity.

摘要

为阐明任何药物置换相互作用的机制,我们研究了甲哌卡因与布比卡因混合物在血清以及白蛋白或α1-酸性糖蛋白溶液中的蛋白结合情况。单独使用甲哌卡因时的蛋白结合数据,在血清中用具有一类结合位点和分配常数的模型能得到最佳描述,在两种分离的蛋白质溶液中则用具有一类结合位点的模型能得到最佳描述。在布比卡因存在的情况下,甲哌卡因在血清中的结合亲和力降低。当研究α1-酸性糖蛋白溶液时,观察到布比卡因对甲哌卡因的置换。证实了典型的竞争性抑制。布比卡因降低了甲哌卡因与白蛋白的结合,但置换程度不显著。当同时给药时,这两种酰胺类局部麻醉药会协同相互作用,产生高于预期的甲哌卡因游离浓度。这种相互作用增加了毒性风险。

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