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苯佐卡因与模型膜的相互作用。

Interaction of benzocaine with model membranes.

作者信息

Pinto L M, Yokaichiya D K, Fraceto L F, de Paula E

机构信息

Departamento de Bioquímica, Instituto de Biologia, Universidade Estadual de Campinas, Sao Paulo, Brazil.

出版信息

Biophys Chem. 2000 Oct 30;87(2-3):213-23. doi: 10.1016/s0301-4622(00)00196-4.

Abstract

We measured the absorption properties, water solubility and partition coefficients (P) between n-octanol, egg phosphatidylcholine (EPC) liposomes and erythrocyte ghosts/water for benzocaine (BZC), an ester-type always uncharged local anesthetic. The interaction of BZC with EPC liposomes was followed using Electron Paramagnetic Resonance, with spin labels at different positions in the acyl chain (5, 7, 12, 16-doxylstearic acid methyl ester). Changes in lipid organization upon BZC addition allowed the determination of P values, without phase separation. The effect of BZC in decreasing membrane organization (maximum of 11.6% at approx. 0.8:1 BZC:EPC) was compared to those caused by the local anesthetics tetracaine and lidocaine. Hemolytic tests revealed a biphasic (protective/inductive) concentration-dependent hemolytic effect for BZC upon rat erythrocytes, with an effective BZC:lipid molar ratio in the membrane for protection (RePROT), onset of hemolysis (ReSAT) and 100% membrane solubilization (ReSOL) of 1.0:1, 1.1:1 and 1.3:1, respectively. The results presented here reinforce the importance of considering hydrophobic interactions in the interpretation of the effects of anesthetics on membranes.

摘要

我们测量了酯型非离子型局部麻醉药苯佐卡因(BZC)的吸收特性、水溶性以及在正辛醇、卵磷脂(EPC)脂质体与红细胞血影/水之间的分配系数(P)。使用电子顺磁共振技术,通过在酰基链不同位置(5, 7, 12, 16-二氧硬脂酸甲酯)标记自旋,跟踪BZC与EPC脂质体的相互作用。添加BZC后脂质组织的变化使得在无相分离的情况下测定P值成为可能。将BZC降低膜组织化的效果(在约0.8:1的BZC:EPC比例下最大降低11.6%)与局部麻醉药丁卡因和利多卡因所引起的效果进行了比较。溶血试验显示,BZC对大鼠红细胞具有双相(保护/诱导)浓度依赖性溶血作用,在膜中起到保护作用(RePROT)、开始溶血(ReSAT)和100%膜溶解(ReSOL)时的有效BZC:脂质摩尔比分别为1.0:1、1.1:1和1.3:1。此处呈现的结果强化了在解释麻醉药对膜的作用时考虑疏水相互作用的重要性。

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