Feldmeyer Dirk, Radnikow Gabriele
Research Centre Jülich, Institute for Neuroscience and Medicine, INM-2, Juelich, Germany.
J Physiol. 2009 May 1;587(Pt 9):1889-96. doi: 10.1113/jphysiol.2009.169458. Epub 2009 Mar 9.
In the neocortex, most excitatory, glutamatergic synapses are established during the first 4-5 weeks after birth. During this period profound changes in the properties of synaptic transmission occur. Excitatory postsynaptic potentials (EPSPs) at immature synaptic connections are profoundly and progressively reduced in response to moderate to high frequency (5-100 Hz) stimulation. With maturation, this frequency-dependent depression becomes progressively weaker and may eventually transform into a weak to moderate EPSP facilitation. In parallel to changes in the short-term plasticity, a reduction in the synaptic reliability occurs at most glutamatergic neocortical synapses: immature synapses show a high probability of neurotransmitter release as indicated by their low failure rate and small EPSP amplitude variation. This high reliability is reduced in mature synapses, which show considerably higher failure rates and more variable EPSP amplitudes. During early neocortical development synaptic vesicle pools are not yet fully differentiated and their replenishment may be slow, thus resulting in EPSP amplitude depression. The decrease in the probability of neurotransmitter release may be the result of an altered Ca(2+) control in the presynaptic terminal with a reduced Ca(2+) influx and/or a higher Ca(2+) buffering capacity. This may lead to a lower synaptic reliability and a weaker short-term synaptic depression with maturation.
在新皮层中,大多数兴奋性谷氨酸能突触在出生后的前4 - 5周内形成。在此期间,突触传递特性会发生深刻变化。在未成熟的突触连接中,对中高频(5 - 100Hz)刺激的兴奋性突触后电位(EPSP)会显著且逐渐降低。随着成熟,这种频率依赖性抑制逐渐减弱,并最终可能转变为轻度到中度的EPSP易化。与短期可塑性变化并行的是,大多数谷氨酸能新皮层突触的突触可靠性降低:未成熟突触显示出高神经递质释放概率,其低失败率和小的EPSP幅度变化表明了这一点。成熟突触的这种高可靠性降低,其显示出相当高的失败率和更可变的EPSP幅度。在新皮层早期发育过程中,突触小泡池尚未完全分化,其补充可能较慢,从而导致EPSP幅度降低。神经递质释放概率的降低可能是由于突触前终末中Ca(2+)控制改变,Ca(2+)内流减少和/或Ca(2+)缓冲能力增强所致。这可能导致较低的突触可靠性和成熟时较弱的短期突触抑制。