Gold M R, Martin A R
J Physiol. 1983 Sep;342:85-98. doi: 10.1113/jphysiol.1983.sp014841.
Voltage-clamp techniques were used to record spontaneously occurring inhibitory post-synaptic currents (i.p.s.c.s) from Müller cells in the brain stem of the lamprey. In normal bathing solution, the i.p.s.c.s in most cells had unimodally distributed amplitudes with a mean corresponding to a peak conductance of 107 nS and a coefficient of variation of about 15%. About 20% of the cells displayed, in addition, events of approximately twice the modal amplitude. The falling phase of the i.p.s.c.s was exponential with a mean time constant of about 32 msec. This is the same as the relaxation time constant of glycine-activated channels in these cells under comparable conditions (Gold & Martin, 1983b). When tetrodotoxin (TTX) was added to the bathing solution the spontaneous i.p.s.c.s disappeared, suggesting that they were due to release of transmitter by action potentials in presynaptic terminals. Spontaneous activity was also abolished by removing Ca2+ from the bathing solution. When extracellular Ca2+ was increased, or 4-aminopyridine (4-AP) was added to the bathing solution, the mean amplitude of the i.p.s.c.s increased and the amplitude distribution showed two or more distinct peaks. Analysis of the amplitude distributions suggested that the peaks represented single and multiple quantal events and that the release process obeyed binomial statistics. In TTX-blocked preparations, spontaneous i.p.s.c.s could be induced by raising extracellular K+. These had the same time constant of decay as in normal solution and a unimodal amplitude distribution, with the mean corresponding to a peak conductance of 45 nS. In solutions with raised extracellular K+ and reduced extracellular Cl-, the mean i.p.s.c. amplitude corresponded to a peak conductance of 67 nS. These variations in conductance corresponded closely to variations in conductance with extracellular K+ and Cl- of single glycine-activated channels. It is concluded that the i.p.s.c.s are produced by activation of conductance channels identical to those activated by glycine, and that in normal bathing solution i.p.s.c.s produced by individual presynaptic action potentials are the result of the release of one or, at most, two quanta of transmitter. Each quantum activates approximately 1500 elementary channels.
采用电压钳技术记录七鳃鳗脑干中缪勒细胞自发产生的抑制性突触后电流(i.p.s.c.s)。在正常的灌流液中,大多数细胞的i.p.s.c.s幅度呈单峰分布,其平均值对应于107 nS的峰值电导,变异系数约为15%。此外,约20%的细胞还出现了幅度约为模式幅度两倍的事件。i.p.s.c.s的下降相呈指数形式,平均时间常数约为32毫秒。这与在类似条件下这些细胞中甘氨酸激活通道的松弛时间常数相同(戈尔德和马丁,1983b)。当向灌流液中加入河豚毒素(TTX)时,自发的i.p.s.c.s消失,这表明它们是由突触前终末动作电位释放递质所致。通过从灌流液中去除Ca2+,自发活动也被消除。当细胞外Ca2+增加或向灌流液中加入4-氨基吡啶(4-AP)时,i.p.s.c.s的平均幅度增加,幅度分布显示出两个或更多不同的峰值。对幅度分布的分析表明,这些峰值代表单个和多个量子事件,且释放过程符合二项式统计。在TTX阻断的标本中,提高细胞外K+可诱导出自发的i.p.s.c.s。这些i.p.s.c.s的衰减时间常数与正常溶液中的相同,幅度分布呈单峰,平均值对应于45 nS的峰值电导。在细胞外K+升高和细胞外Cl-降低的溶液中,i.p.s.c.的平均幅度对应于67 nS的峰值电导。这些电导变化与单个甘氨酸激活通道的细胞外K+和Cl-电导变化密切相关。得出的结论是,i.p.s.c.s是由与甘氨酸激活的通道相同的电导通道激活产生的,并且在正常灌流液中,单个突触前动作电位产生的i.p.s.c.s是释放一个或至多两个递质量子的结果。每个量子激活约1500个基本通道。