Woodson P B, Schlapfer W T, Tremblay J P, Barondes S H
Brain Res. 1976 Jun 4;109(1):21-40. doi: 10.1016/0006-8993(76)90378-4.
Transmitter release (R) at a synpase in Aplysia californica can be analyzed in terms of a model with the following parameters: A, the available pool of transmitter; F, the fraction of available pool released by a presynaptic action potential; M, the rate of transmitter mobilization into the available pool; D, the rate constant of demobilization of transmitter from the available pool. In the present paper we show that: (1) beginning with an analysis of the recovery from depression of the second of a pair of disolated EPSPs separated by a series of intervals of about 10-60 sec, and assuming that the recovery is due to refilling of a depleted A, it is possible to estimate resting equilibrium values of these parameters; (2) changes in these parameters when a new equilbrium state is reached after prolonged stimulation (e.g., 300 stimuli at 1/sec) can then be quantitatively determined; (3) the increased rate of transmitter release observed during and after repetitive stimulation is the consequence of increases in F and M with changes in A passively following; and (4) there are significant correlations among certain resting parameters and between the values of certain resting parameters and these parameters upon stimulation. Preparations with a large resting F tend to have a relatively small resting A. Preparations with a large resting F or M tend to increase these less with stimulation than preparations with smaller resting values of these parameters. Preparations with large stimulus-dependent increases in F tend to have large stimulus-dependent increases in M.
加利福尼亚海兔突触处的递质释放(R)可依据具有以下参数的模型进行分析:A,递质的可用池;F,由突触前动作电位释放的可用池部分;M,递质向可用池的动员速率;D,递质从可用池的解动员速率常数。在本文中我们表明:(1)从分析一对间隔约10 - 60秒的孤立兴奋性突触后电位(EPSP)中第二个EPSP从抑制中恢复开始,并假设恢复是由于耗尽的A重新填充,就有可能估计这些参数的静息平衡值;(2)在长时间刺激(例如,以1次/秒的频率施加300次刺激)后达到新的平衡状态时,这些参数的变化随后可被定量确定;(3)在重复刺激期间及之后观察到的递质释放速率增加是F和M增加以及A被动随之变化的结果;(4)某些静息参数之间以及某些静息参数的值与刺激时这些参数的值之间存在显著相关性。静息F较大的制剂往往静息A相对较小。静息F或M较大的制剂与这些参数静息值较小的制剂相比,刺激时这些参数的增加往往较少。刺激依赖性F增加较大的制剂往往刺激依赖性M增加也较大。