Farrugia G, Rae J L
Department of Physiology and Biophysics, Mayo Foundation, Rochester, Minnesota 55905.
J Membr Biol. 1992 Jul;129(1):99-107. doi: 10.1007/BF00232058.
The effects of cyclic GMP (cGMP), carbachol and diltiazem on a potassium-selective, delayed-rectifier current in freshly dissociated rabbit corneal epithelial cells were studied using a modified perforated-patch-clamp technique. The current was stimulated by both 500 microM cGMP (2.3-4.5-fold, mean = 2.9) and 250 nM carbachol, a muscarinic agonist (1.12-7.04-fold, mean = 3.8), and the stimulated current was totally blocked by diltiazem (10 microM). The effects of cGMP appeared to be, at least in part, different from those of carbachol as they required the presence of external calcium. Single-channel data suggest that cGMP and carbachol activate the potassium current by increasing the open probability of the channel via a second-messenger system and that the action of diltiazem is probably through a direct blocking effect on the open channel.
采用改良的穿孔膜片钳技术,研究了环磷酸鸟苷(cGMP)、卡巴胆碱和地尔硫䓬对新鲜分离的兔角膜上皮细胞中钾选择性延迟整流电流的影响。500微摩尔/升的cGMP(2.3 - 4.5倍,平均值 = 2.9)和250纳摩尔/升的卡巴胆碱(一种毒蕈碱激动剂,1.12 - 7.04倍,平均值 = 3.8)均可刺激该电流,且刺激电流可被10微摩尔/升的地尔硫䓬完全阻断。cGMP的作用似乎至少部分不同于卡巴胆碱,因为它们需要细胞外钙的存在。单通道数据表明,cGMP和卡巴胆碱通过第二信使系统增加通道的开放概率来激活钾电流,而地尔硫䓬的作用可能是通过对开放通道的直接阻断作用。