Larkman A, Hannay T, Stratford K, Jack J
University Laboratory of Physiology, Oxford University, UK.
Nature. 1992 Nov 5;360(6399):70-3. doi: 10.1038/360070a0.
The quantal hypothesis proposes that chemical synaptic transmission involves the probabilistic release of multimolecular packets of transmitter. Analysis of the resulting trial-to-trial fluctuations in postsynaptic response can provide estimates both of the number of quanta released and of the size of their postsynaptic effect. This in turn permits the quantification of the relative contributions of pre- and postsynaptic factors to the strength of a given synapse. Quantal analysis of excitatory synapses in the hippocampus has proved difficult and has led to contradictory conclusions when applied to long-term potentiation. Here we report the use of a combination of quantal analysis procedures to provide evidence that both pre- and postsynaptic changes can contribute substantially to the maintenance of long-term potentiation in the CA1 region of the hippocampus. The initial setting of the presynaptic release mechanism seems to determine their relative importance.
量子假说提出,化学性突触传递涉及递质多分子包的概率性释放。对由此产生的突触后反应中逐次试验波动的分析,既可以估计释放的量子数量,也可以估计其突触后效应的大小。这反过来又能够量化突触前和突触后因素对给定突触强度的相对贡献。事实证明,对海马体中兴奋性突触进行量子分析很困难,并且在应用于长时程增强时得出了相互矛盾的结论。在此,我们报告使用了多种量子分析程序的组合,以提供证据表明突触前和突触后变化都可能对海马体CA1区的长时程增强维持有重大贡献。突触前释放机制的初始设定似乎决定了它们的相对重要性。