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Interactions of Veratrum Alkaloids, Procaine, and Calcium with Monolayers of Stearic Acid and Their Implications for Pharmacological Action

机译:藜芦生物碱,普鲁卡因和钙与硬脂酸单层的相互作用及其对药理作用的影响

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摘要

The interactions of veratridine, cevadine, veracevine, and veratramine with monolayers of stearic acid show marked differences. Veratridine and cevadine, at concentrations that are known from potential, ionic flux, and other measurements to affect living membranes, react strongly with the film and appear to cause an "interfacial dissolution" whereby both the alkaloid and the stearate leave the surface. Veracevine at the same concentration does not interact with the film. The veratramine reaction is weak, much like that of the local anesthetic procaine. The veratridine and cevadine effects are antagonized by 10-3 M Ca++, low pH, and 3.7 and 7.4 x 10-3 M procaine. These differences among the veratrum alkaloids and the antagonisms parallel effects observed in living systems. Such parallelism suggests that similar physical interactions are involved in the stearate film and in natural membranes.
机译:Veratridine,Cevadine,Veracevine和Veratramine与硬脂酸单层的相互作用显示出显着差异。从电位,离子通量和其他测量结果已知会影响活膜的浓度的Veratridine和Cevadine会与薄膜发生强烈反应,并似乎引起“界面溶解”,从而使生物碱和硬脂酸酯均离开表面。浓度相同的Veracevine不会与胶片相互作用。维他命胺反应微弱,很像局部麻醉的普鲁卡因。 10-3 M Ca ++,低pH值和3.7 x 7.4 x 10-3 M普鲁卡因可拮抗维拉替丁和西伐他汀的作用。藜芦生物碱之间的这些差异和在生物系统中观察到的拮抗作用平行。这种平行性表明,硬脂酸酯薄膜和天然膜中也存在类似的物理相互作用。

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