Bolshakov V Y, Golan H, Kandel E R, Siegelbaum S A
Department of Pharmacology, Howard Hughes Medical Institute, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Neuron. 1997 Sep;19(3):635-51. doi: 10.1016/s0896-6273(00)80377-3.
Long-term potentiation at CA3-CA1 hippocampal synapses exhibits an early phase and a late phase, which can be distinguished by their underlying molecular mechanisms. Unlike the early phase, the late phase is dependent on both cAMP and protein synthesis. Quantal analysis of unitary synaptic transmission between a single presynaptic CA3 neuron and a single postsynaptic CA1 neuron suggests that, under certain conditions, the early phase of LTP involves an increase in the probability of release of a single quantum of transmitter from a single presynaptic release site, with no change in the number of quanta that are released or in postsynaptic sensitivity to transmitter. Here, we show that the cAMP-induced late phase of LTP involves an increase in the number of quanta released in response to a single presynaptic action potential, possibly due to an increase in the number of sites of synaptic transmission between a single CA3 and a single CA1 neuron.
海马体CA3-CA1突触处的长时程增强(LTP)表现出早期阶段和晚期阶段,这两个阶段可通过其潜在的分子机制加以区分。与早期阶段不同,晚期阶段依赖于环磷酸腺苷(cAMP)和蛋白质合成。对单个突触前CA3神经元与单个突触后CA1神经元之间的单突触传递进行量子分析表明,在某些条件下,LTP的早期阶段涉及单个突触前释放位点释放单个量子递质的概率增加,而释放的量子数量或突触后对递质的敏感性没有变化。在此,我们表明,cAMP诱导的LTP晚期阶段涉及单个突触前动作电位引发的释放量子数量增加,这可能是由于单个CA3神经元与单个CA1神经元之间突触传递位点数量增加所致。