Gillis K D, Misler S
Department of Medicine (Jewish Hospital), Washington University Medical Center, St. Louis, Mo. 63110.
Pflugers Arch. 1993 Jul;424(2):195-7. doi: 10.1007/BF00374612.
We have investigated the effects of cAMP-enhancing agents on depolarization-induced membrane capacitance increases (delta Cm) in single rat pancreatic B-cells. Concentrations of IBMX, 8-CPT cAMP and forskolin, which enhance cAMP and insulin release, all enhance depolarization-induced delta Cm's seen in response to single voltage-clamp pulses and reduce the depression of delta Cm responses often seen with trains of pulses. These effects often occur in the absence of changes in peak Ca2+ current or the total Ca2+ charge entry during the depolarizing pulse. These data suggest that cAMP-modulating maneuvers may directly affect the mechanism of insulin granule mobilization into a readily releasible store or fusion at a discharge site.
我们研究了环磷酸腺苷(cAMP)增强剂对单个大鼠胰腺β细胞去极化诱导的膜电容增加(δCm)的影响。可增强cAMP和胰岛素释放的异丁基甲基黄嘌呤(IBMX)、8-氯苯基硫代-cAMP(8-CPT cAMP)和福斯可林的浓度,均能增强单个电压钳脉冲诱发的去极化诱导的δCm,并减少脉冲串常出现的δCm反应的抑制。这些效应通常在去极化脉冲期间峰值Ca2+电流或总Ca2+电荷进入无变化的情况下出现。这些数据表明,cAMP调节策略可能直接影响胰岛素颗粒动员到易于释放的储存库或在释放位点融合的机制。