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Cholesterol and Cardiolipin Importance in Local Anesthetics–Membrane Interactions: The Langmuir Monolayer Study

机译:局麻药与膜相互作用中胆固醇和心磷脂的重要性:Langmuir单层研究

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摘要

Local anesthetics (LAs) are known to act on membrane level; however, the molecular mechanism of their activity is still not fully understood. One hypothesis holds that these drugs can incorporate into lipid membrane of nerve cells and in this way change conformation of channel proteins responsible for transport of sodium ions. However, the action of anesthetics is not limited to nerve cells. These drugs also affect other types of cells and organelles, causing severe side effects. In this paper, we applied Langmuir monolayers—as model of cellular membranes—and investigated interactions between selected amide-type local anesthetics (lidocaine prilocaine, mepivacaine and ropivacaine, in the form of hydrochlorides) and lipid components of natural membranes: cholesterol, POPC and cardiolipin (CL) and their mixtures (POPC/cholesterol and POPC/CL/cholesterol), which can serve as simplified models of nerve cell membranes, erythrocytes, and mitochondria. The influence of the drug was monitored by registering the surface pressure (π) as a function of surface area per molecule (A) in a monolayer in the presence of the drug in the subphase. The structure of lipid monolayers on subphases containing and devoid of the studied drugs were visualized with Brewster angle microscopy (BAM). Langmuir monolayer studies complemented with surface visualization technique reveal the expansion and fluidization of lipid monolayers, with the most pronounced effect observed for cardiolipin. In mixed systems, the effect of LAs was found to depend on cholesterol proportion. The observed fluidization of membranes by local anesthetics may negatively affect cells functioning and therefore can explain side effects of these drugs both on the cardiovascular and nervous systems.Electronic supplementary materialThe online version of this article (10.1007/s00232-018-0055-6) contains supplementary material, which is available to authorized users.
机译:已知局部麻醉药(LAs)在膜水平起作用。然而,其活性的分子机制仍不完全清楚。一种假设认为,这些药物可以掺入神经细胞的脂质膜,并以此方式改变负责钠离子转运的通道蛋白的构象。但是,麻醉药的作用不仅限于神经细胞。这些药物还会影响其他类型的细胞和细胞器,导致严重的副作用。在本文中,我们将Langmuir单层膜作为细胞膜的模型,并研究了选定的酰胺类局部麻醉药(利多卡因,丙胺卡因和米哌卡因和罗哌卡因,以盐酸盐的形式)与天然膜的脂质成分(胆固醇,POPC和心磷脂(CL)及其混合物(POPC /胆固醇和POPC / CL /胆固醇),可作为神经细胞膜,红细胞和线粒体的简化模型。通过在子相中存在药物的情况下,将表面压力(π)记录为单层中每分子表面积(A)表面积的函数来监测药物的影响。用布鲁斯特角显微镜(BAM)观察含有和不含研究药物的亚相上脂质单层的结构。 Langmuir单层研究与表面可视化技术相辅相成,揭示了脂质单层的膨胀和流态化,其中心磷脂的作用最为明显。在混合系统中,发现LAs的作用取决于胆固醇比例。局部麻醉药观察到的膜流化可能会对细胞功能产生负面影响,因此可以解释这些药物对心血管和神经系统的副作用。电子补充材料本文的在线版本(10.1007 / s00232-018-0055-6)包含补充材料,授权用户可以使用。

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