Reinhard U, Büchi J, Perlia X
Arzneimittelforschung. 1975 Sep;25(9):1340-51.
The general part consists of a review on nerve stimulus mechanism as well as the nerve structure and the function of nerve membrane as the site of action of local anesthetics. Furthermore a possibility of interaction between local anesthetics and the membrane components especially phospholipids is discussed. These phospholipids show interesting properties with respect to ions as well as local-anesthetics, which allow us to suppose that they are important participants in nervous stimulus transmission. In the experimental part two methods are described. The first deals with the measurement of electrical resistance as function of time at cephalin and cholesterin impregnated filter membrane in solutions of cinchocain homologues. An increase in the resistance with the increase in concentration of test substances was observed. The same was the effect of increasing chain length in alkoxy group where after butoxy derivative, a deformation of membrane was observed. In the second method the drug binding capacity of cephalin dispersed in aqueous medium was measured. Here, too, the increase in the binding capacity with the increase in alkoxy chain was observed. The large difference in free binding energy between two subsequent homologues is explained as the effect of increase in van der Waals' forces and hydrophobic interactions on one hand, and a change in colloidal form of cephalin dispersion on the other hand.
总论部分包括对神经刺激机制、神经结构以及作为局部麻醉药作用部位的神经膜功能的综述。此外,还讨论了局部麻醉药与膜成分尤其是磷脂之间相互作用的可能性。这些磷脂在离子和局部麻醉药方面表现出有趣的特性,这使我们推测它们是神经刺激传递的重要参与者。实验部分描述了两种方法。第一种方法涉及在辛可卡因同系物溶液中,测量在脑磷脂和胆固醇浸渍的滤膜上电阻随时间的变化。观察到随着测试物质浓度的增加电阻增大。烷氧基链长度增加也有同样的效果,丁氧基衍生物之后观察到膜的变形。第二种方法是测量分散在水介质中的脑磷脂的药物结合能力。在此也观察到随着烷氧基链长度增加结合能力增强。两个连续同系物之间自由结合能的巨大差异一方面解释为范德华力和疏水相互作用增加的结果,另一方面解释为脑磷脂分散体胶体形式的变化。