Bezprozvanny I, Bezprozvannaya S, Ehrlich B E
Department of Medicine, University of Connecticut, Farmington 06030-1305.
Mol Biol Cell. 1994 Jan;5(1):97-103. doi: 10.1091/mbc.5.1.97.
Effects of the xanthine drug caffeine on inositol (1,4,5)-trisphosphate (InsP3)-gated calcium (Ca) channels from canine cerebellum were studied using single channels incorporated into planar lipid bilayers. Caffeine, used widely as an agonist of ryanodine receptors, inhibited the activity of InsP3-gated Ca channels in a noncooperative fashion with half-inhibition at 1.64 mM caffeine. The frequency of channel openings was decreased more than threefold after addition of 5 mM caffeine; there was only a small effect on mean open time of the channels, and the single channel conductance was unchanged. Increased InsP3 concentration overcame the inhibitory action of caffeine, but caffeine did not reduce specific [3H]InsP3 binding to the receptor. The inhibitory action of caffeine on InsP3 receptors suggests that the action of caffeine on the intracellular Ca pool must be interpreted with caution when both ryanodine receptors and InsP3 receptors are present in the cell.
利用整合到平面脂质双分子层中的单通道,研究了黄嘌呤药物咖啡因对犬小脑肌醇(1,4,5)-三磷酸(InsP3)门控钙(Ca)通道的影响。咖啡因作为ryanodine受体的激动剂被广泛使用,它以非协同方式抑制InsP3门控钙通道的活性,在1.64 mM咖啡因时出现半数抑制。加入5 mM咖啡因后,通道开放频率降低了三倍多;对通道的平均开放时间只有很小的影响,单通道电导没有变化。InsP3浓度的增加克服了咖啡因的抑制作用,但咖啡因并没有降低[3H]InsP3与受体的特异性结合。咖啡因对InsP3受体的抑制作用表明,当细胞中同时存在ryanodine受体和InsP3受体时,咖啡因对细胞内钙库的作用必须谨慎解释。