Hehl S, Neumcke B
I. Physiologisches Institut, Universität des Saarlandes, Homburg/Saar, Germany.
Eur Biophys J. 1993;22(1):1-4. doi: 10.1007/BF00205806.
Blockage of ATP-sensitive K+ channels by various drugs has been reported to exhibit a weak concentration dependence with Hill coefficients below unity. This phenomenon is interpreted by a negative cooperativity between K+ channels whereby drug binding to one channel lowers the drug affinities of neighbouring channels. Results are presented for a dimeric and a tetrameric channel model and compared with published experimental data.
据报道,各种药物对ATP敏感性钾通道的阻断表现出较弱的浓度依赖性,希尔系数低于1。这种现象被解释为钾通道之间的负协同作用,即药物与一个通道的结合会降低相邻通道的药物亲和力。给出了二聚体和四聚体通道模型的结果,并与已发表的实验数据进行了比较。