Larkman A, Stratford K, Jack J
University Laboratory of Physiology, Oxford University, UK.
Nature. 1991 Mar 28;350(6316):344-7. doi: 10.1038/350344a0.
Quantal analysis can provide a quantitative description of important aspects of chemical synaptic transmission and its modification. The technique has recently been applied to excitatory synapses within the hippocampus, especially the form of synaptic plasticity known as long-term potentiation. However, these attempts have met with only limited success, in that the individual quantal amplitudes making up the synaptic response generally could not be resolved. Here we have paid attention to the possible instability of the quantal fluctuation pattern over time. We were able to resolve individual quantal component amplitudes for a high proportion of the experiments, and so demonstrate the quantal nature of excitatory transmission in the CA1 region of the hippocampus. Mean quantal amplitudes for individual excitatory postsynaptic potentials were 84-197 microV, with a mean of 131 +/- 29 microV. For periods during which the fluctuation pattern was stable, the variance associated with individual quantal amplitudes was low. We have also used quantal analysis to show that synaptic depression following prolonged stimulation at these synapses is primarily a presynaptic phenomenon.
量子分析可以对化学突触传递及其修饰的重要方面进行定量描述。该技术最近已应用于海马体内的兴奋性突触,尤其是称为长时程增强的突触可塑性形式。然而,这些尝试仅取得了有限的成功,因为构成突触反应的单个量子幅度通常无法分辨。在这里,我们关注了量子波动模式随时间可能存在的不稳定性。我们能够在很大比例的实验中分辨出单个量子成分的幅度,从而证明海马体CA1区兴奋性传递的量子性质。单个兴奋性突触后电位的平均量子幅度为84 - 197微伏,平均为131±29微伏。在波动模式稳定的时期,与单个量子幅度相关的方差较低。我们还使用量子分析表明,在这些突触处长时间刺激后的突触抑制主要是一种突触前现象。