Trautmann A
Proc R Soc Lond B Biol Sci. 1983 May 23;218(1211):241-51. doi: 10.1098/rspb.1983.0037.
At the frog neuromuscular junction, a dose-response curve for the activation of the nicotinic receptor by carbachol has been determined under conditions where desensitization could be estimated and corrected for. The value of the Hill coefficient was 2 and that of the dissociation constant for carbachol was 400 microM, the two binding sites of the receptor being assumed identical. The properties of six cholinergic agonists were then compared. the potencies and mean open times of these agonists are ranked in the same order, but the range of the potencies is much larger (1-200) than that of the mean open times (1-4). The differences in the properties of the different agonists could simply be due to differences in the rate of dissociation of the agonists, if it is assumed that one apparent opening of the channel is in fact a burst of several oscillations between the open and closed conformations, such that a burst is interrupted by the dissociation of one agonist molecule.
在青蛙神经肌肉接头处,已在可估计和校正脱敏作用的条件下,确定了卡巴胆碱激活烟碱受体的剂量反应曲线。希尔系数的值为2,卡巴胆碱的解离常数为400微摩尔,假定受体的两个结合位点相同。然后比较了六种胆碱能激动剂的特性。这些激动剂的效力和平均开放时间按相同顺序排列,但效力范围(1 - 200)比平均开放时间范围(1 - 4)大得多。如果假设通道的一次明显开放实际上是在开放和关闭构象之间的几次振荡爆发,以至于一次爆发会因一个激动剂分子的解离而中断,那么不同激动剂特性的差异可能仅仅是由于激动剂解离速率的差异。