Dilger J P, Brett R S
Department of Anesthesiology, State University of New York, Stony Brook 11794-8480.
Biophys J. 1990 Apr;57(4):723-31. doi: 10.1016/S0006-3495(90)82593-5.
Using the outside-out patch clamp recording technique together with a rapid solution exchange system, we measured ionic currents through nicotinic acetylcholine (ACh) receptor channels from BC3H-1 cells in response to rapid applications of 0.3-1,000 microM ACh. We used nonstationary fluctuation analysis of ensembles of responses to deduce the number of channels in the patch, the maximum open channel probability as a function of ACh concentration and the time course of a fast desensitization process. We found that: (a) Excised patches from BC3H-1 cells typically contain between 50 and 150 functional ACh receptor ion channels. (b) The open channel probability is proportional to [ACh]1.95 at low concentrations of ACh, is half-maximal at 20 microM ACh and saturates above 100 microM ACh. (c) ACh is a very efficacious agonist; 100 microM ACh opens at least 90% of the available channels. This estimate of efficacy is model-independent. (d) The rate of decay of the agonist-induced current is concentration-dependent. In the presence of 100 microM ACh the current decays with a time constant of 50-100 ms. It decays more slowly in the presence of lower concentrations of agonist but is relatively insensitive to voltage.
我们使用外向式膜片钳记录技术并结合快速溶液交换系统,测量了BC3H - 1细胞中烟碱型乙酰胆碱(ACh)受体通道的离子电流,以响应快速施加的0.3 - 1000微摩尔/升的ACh。我们对一系列响应进行非平稳波动分析,以推断膜片中通道的数量、最大开放通道概率作为ACh浓度的函数以及快速脱敏过程的时间进程。我们发现:(a)从BC3H - 1细胞中切除的膜片通常含有50至150个功能性ACh受体离子通道。(b)在低浓度ACh时,开放通道概率与[ACh]的1.95次方成正比,在20微摩尔/升ACh时达到最大值的一半,在100微摩尔/升ACh以上时达到饱和。(c)ACh是一种非常有效的激动剂;100微摩尔/升的ACh可打开至少90%的可用通道。这种对效力的估计与模型无关。(d)激动剂诱导电流的衰减速率与浓度有关。在100微摩尔/升ACh存在下,电流以50 - 100毫秒的时间常数衰减。在较低浓度激动剂存在下,它衰减得更慢,但对电压相对不敏感。