Tanaka H, Matsunaga K, Kawazura H
Faculty of Pharmaceutical Sciences, Josai University, Saitama, Japan.
Biophys J. 1992 Aug;63(2):569-72. doi: 10.1016/S0006-3495(92)81629-6.
A dynamic 23Na nuclear magnetic resonance (NMR) technique was applied to the exchange system of Na+ ions present inside and outside large unilamellar vesicles at an equivalent concentration. Addition of melittin to phosphatidylcholine vesicles did not induce any detectable Na+ transport across the membrane but subsequent addition of a trace of chlorpromazine or imipramine did induce Na+ transport. Because the formation of a drug-melittin adduct in a solution was detected by 1H NMR, the activation of melittin channels was assumed to originate from the direct interaction of the drug and melittin.
一种动态23Na核磁共振(NMR)技术被应用于等浓度存在于大单层囊泡内外的Na+离子交换系统。向磷脂酰胆碱囊泡中添加蜂毒素不会诱导任何可检测到的Na+跨膜转运,但随后添加微量的氯丙嗪或丙咪嗪确实会诱导Na+转运。由于通过1H NMR检测到溶液中药物 - 蜂毒素加合物的形成,因此推测蜂毒素通道的激活源于药物与蜂毒素的直接相互作用。