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八种钙通道阻滞剂对由大鼠脑总脂质制备的脂质体膜的扰动作用。

Perturbation effect of eight calcium channel blockers on liposomal membranes prepared from rat brain total lipids.

作者信息

Ondrias K, Ondriasová E, Stasko A

机构信息

Institute of Experimental Pharmacology, Slovak Academy of Sciences, Bratislava, CSFR.

出版信息

Chem Phys Lipids. 1992 Jul;62(1):11-7. doi: 10.1016/0009-3084(92)90049-u.

Abstract

EPR spectroscopy of phosphatidylcholine or stearic acid labeled at the doxyl group at the 16-carbon position was used to compare the perturbation effect of eight calcium channel blockers (CB) on overall dynamics/disorder of the hydrophobic part of liposome membranes prepared from rat brain total lipids at the drug/lipid molar ratio of 1/2. Nifedipine (NIF), nimodipine, niludipine and nitrendipine had a minor effect on the dynamics/disorder of the liposome membranes, whereas the disordering effect of verapamil (VER), mepamil, gallopamil and diltiazem was more pronounced. Concentration dependence of the overall disordering effect of VER on liposomal membranes was found at the VER/lipid ratio greater than 0.02 and for the tranquilizer thioridazine greater than 0.005. VER exerted a disordering effect at the hydrophobic part of synaptosomal membranes at concentrations greater than or equal to 0.32 mmol/l, whereas NIF did not exhibit a disordering effect even at concentrations of 10-20 mmol/l.

摘要

采用电子顺磁共振光谱法(EPR)研究了在16-碳位置的多昔基团处标记的磷脂酰胆碱或硬脂酸,以比较八种钙通道阻滞剂(CB)对由大鼠脑总脂质制备的脂质体膜疏水部分的整体动力学/无序性的扰动效应,药物/脂质摩尔比为1/2。硝苯地平(NIF)、尼莫地平、尼鲁地平及尼群地平对脂质体膜的动力学/无序性影响较小,而维拉帕米(VER)、美帕米、加洛帕米及地尔硫䓬的无序化作用更为显著。当VER/脂质比大于0.02以及安定药硫利达嗪大于0.005时,发现VER对脂质体膜的整体无序化效应存在浓度依赖性。当浓度大于或等于0.32 mmol/L时,VER对突触体膜的疏水部分产生无序化作用,而即使在10 - 20 mmol/L的浓度下,NIF也未表现出无序化作用。

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