An NMR study of the structural basis of the wide range of pharmacological functions of acetylsalicylic acid.

J Li, H Huang, M Zhou, S Ning, X Jiang, Y Peng, K Zhao
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引用次数: 4

Abstract

The interaction between acetylsalicylic acid (aspirin) and membrane was studied by NMR spectra. (1) NMR spectra showed acetylsalicylic acid did not insert into membrane; (2) 1H NMR spectrum recorded by spin-echo pulse sequence showed protons of the aromatic ring interacted with membrane; (3) the change of spin-lattice relaxation (T1) of 31P was ascribed to the association of acetylsalicylic acid to the polar head of lecithin; (4) the self-diffusion coefficient measured by pulsed field gradients NMR showed the mobility of acetylsalicylic acid was restricted by membrane and that acetylsalicylic acid changed membrane viscosity. Based on the results, the relationship between the interaction and the mechanism of the wide pharmacological functions of acetylsalicylic acid is discussed.

核磁共振研究了乙酰水杨酸广泛的药理功能的结构基础。
采用核磁共振光谱法研究了乙酰水杨酸(阿司匹林)与膜的相互作用。(1)核磁共振显示乙酰水杨酸未插入膜内;(2)自旋回波脉冲序列记录的1H NMR谱显示芳香环的质子与膜相互作用;(3) 31P的自旋-晶格弛豫(T1)的变化归因于乙酰水杨酸与卵磷脂极性头的缔合;(4)脉冲场梯度核磁共振测量的自扩散系数表明,乙酰水杨酸的迁移受到膜的限制,乙酰水杨酸改变了膜的粘度。在此基础上,讨论了乙酰水杨酸的相互作用关系及其广泛药理作用的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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