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两种局部麻醉药与磷脂膜和非红细胞血影蛋白的差异相互作用:在胆固醇和神经节苷脂GM1存在下的定位

Differential interactions of two local anesthetics with phospholipid membrane and nonerythroid spectrin: Localization in presence of cholesterol and ganglioside, GM1.

作者信息

Chakrabarti Abhijit, Patra Malay

机构信息

Crystallography & Molecular Biology Division, Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata 700064, India.

Chemistry Department, University of Calcutta 92, A. P. C Road, Kolkata 700009, India.

出版信息

Biochim Biophys Acta. 2015 Mar;1848(3):821-32. doi: 10.1016/j.bbamem.2014.11.022. Epub 2014 Dec 5.

Abstract

Interactions of two local anesthetics, dibucaine and tetracaine have been studied with phospholipid vesicles containing cholesterol and/or monosialogangliosides (GM1) using fluorescence spectroscopy. The fluorescence intensity of tetracaine showed a marked increase with the increasing molar ratio of the phospholipid to tetracaine, while that of dibucaine showed opposite effects. Steady state anisotropy and the wavelength of maximum emission (λmax) decreased with the increasing phospholipids to tetracaine ratio. The extent of such changes in anisotropy and λmax in the presence and absence of two important components of neuronal membranes, cholesterol and GM1 indicated differential membrane localization of the two local anesthetics. To understand the intercellular mode of action of local anesthetics, we have also studied the interactions of dibucaine and tetracaine with brain spectrin which indicate differential spectrin interactions with similar binding strength. Thermodynamic parameters associated with such binding reveal that binding is favored by entropy. Tetracaine brings about distinct structural changes in spectrin compared to dibucaine, as reflected in the tryptophan mean lifetime and far-UV CD spectra. Tetracaine also exhibits a detergent-like property inducing concentration dependent decrease in spectrin anisotropy, further indicating structural changes in brain spectrin with probable implications in its anesthetic potential.

摘要

使用荧光光谱法,研究了两种局部麻醉剂丁卡因和地布卡因与含有胆固醇和/或单唾液酸神经节苷脂(GM1)的磷脂囊泡的相互作用。随着磷脂与丁卡因摩尔比的增加,丁卡因的荧光强度显著增加,而地布卡因的荧光强度则呈现相反的变化。随着磷脂与丁卡因比例的增加,稳态各向异性和最大发射波长(λmax)降低。在存在和不存在神经元膜的两个重要成分胆固醇和GM1的情况下,各向异性和λmax的这种变化程度表明了两种局部麻醉剂在膜中的定位差异。为了了解局部麻醉剂的细胞间作用模式,我们还研究了地布卡因和丁卡因与脑血影蛋白的相互作用,结果表明它们与血影蛋白的相互作用存在差异,但结合强度相似。与这种结合相关的热力学参数表明,结合受熵的影响。与地布卡因相比,丁卡因会使血影蛋白发生明显的结构变化,这在色氨酸平均寿命和远紫外圆二色光谱中得到了体现。丁卡因还表现出类似去污剂的性质,导致血影蛋白各向异性浓度依赖性降低,进一步表明脑血影蛋白的结构变化可能与其麻醉潜力有关。

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