Nilsson T, Schultz V, Berggren P O, Corkey B E, Tornheim K
Rolf Luft Center for Diabetes Research, Department of Molecular Medicine, Karolinska Institute, Karolinska Hospital, Stockholm, Sweden.
Biochem J. 1996 Feb 15;314 ( Pt 1)(Pt 1):91-4. doi: 10.1042/bj3140091.
Closure of ATP-sensitive K+ (K(ATP)) channels is part of the stimulus-secretion coupling mechanism in the pancreatic beta-cell, leading to membrane depolarization and influx of Ca2+ through voltage-sensitive L-type Ca2+ channels. The elevated ATP/ADP ratio seen in the presence of high levels of glucose has been postulated to mediate the glucose-induced closure of the K(ATP) channels and rise in cytoplasmic free Ca2+ concentration ([Ca2+]i), or alternatively to be a consequence of activation of mitochondrial dehydrogenases by the increase in [Ca2+]i. To distinguish between these two possibilities, the time course of the change in the ATP/ADP ratio was determined in comparison with that of [Ca2+]i. We here show that a severalfold rise in the ATP/ADP ratio occurs rapidly on stimulation of suspensions of mouse pancreatic beta-cells with glucose. The change in the ATP/ADP ratio is an early event that begins within 20-40 s and precedes the rise in [Ca2+]i. The temporal relationship indicates that the adenine nucleotide changes cannot be a consequence of the [Ca2+]i changes and may indeed be the connecting link between glucose metabolism and [Ca2+]i changes. When the cells were sequentially treated with high glucose concentration, clonidine and finally high extracellular Ca2+ concentration to induce synchronized oscillations in [Ca2+]i in the cell suspension, corresponding oscillations in the ATP/ADP ratio were observed. Glucose 6-phosphate levels oscillated out of phase with the ATP/ADP ratio. These results support the hypothesis that the Ca2+ oscillations previously observed in glucose-stimulated single islets or beta-cells may reflect oscillations in the ATP/ADP ratio that accompany oscillatory glycolysis.
ATP敏感性钾通道(K(ATP)通道)的关闭是胰腺β细胞刺激-分泌偶联机制的一部分,会导致膜去极化以及Ca2+通过电压敏感性L型Ca2+通道内流。在高血糖水平下观察到的ATP/ADP比值升高,被认为介导了葡萄糖诱导的K(ATP)通道关闭以及细胞质游离Ca2+浓度([Ca2+]i)升高,或者是[Ca2+]i升高激活线粒体脱氢酶的结果。为了区分这两种可能性,我们测定了ATP/ADP比值变化的时间进程,并与[Ca2+]i的变化时间进程进行比较。我们在此表明,用葡萄糖刺激小鼠胰腺β细胞悬液时,ATP/ADP比值会迅速升高数倍。ATP/ADP比值的变化是一个早期事件,在20 - 40秒内开始,先于[Ca2+]i的升高。这种时间关系表明,腺嘌呤核苷酸的变化不是[Ca2+]i变化的结果,实际上可能是葡萄糖代谢与[Ca2+]i变化之间的联系环节。当细胞依次用高葡萄糖浓度、可乐定处理,最后用高细胞外Ca2+浓度处理,以诱导细胞悬液中[Ca2+]i的同步振荡时,观察到了ATP/ADP比值的相应振荡。6-磷酸葡萄糖水平与ATP/ADP比值呈不同步振荡。这些结果支持了以下假设:先前在葡萄糖刺激的单个胰岛或β细胞中观察到的Ca2+振荡,可能反映了伴随振荡性糖酵解的ATP/ADP比值振荡。