Buchanan Katherine A, Mellor Jack R
MRC Centre for Synaptic Plasticity, Department of Anatomy, University of Bristol, University Walk, Bristol BS8 1TD, UK.
J Physiol. 2007 Dec 1;585(Pt 2):429-45. doi: 10.1113/jphysiol.2007.142984. Epub 2007 Oct 11.
Coincident pre- and postsynaptic activity induces synaptic plasticity at the Schaffer collateral synapse onto CA1 pyramidal neurones. The precise timing, frequency and number of coincident action potentials required to induce synaptic plasticity is currently unknown. In this study we show that the postsynaptic activity required for the induction of long-term potentiation (LTP) changes with development. In acute slices from adult rats, coincident pre- and postsynaptic theta burst stimulation (TBS) induced LTP and we show that multiple high-frequency postsynaptic spikes are required. In contrast, in acute slices from juvenile (P14) rats, TBS failed to induce LTP unless the excitatory postsynaptic potentials (EPSPs) were of sufficient magnitude to initiate action potentials. We also show that coincident individual pre- and postsynaptic action potentials are only capable of inducing LTP in the juvenile when given at a frequency greater than 5 Hz and that the timing of individual pre- and postsynaptic action potentials relative to one another is not important. Finally, we show that local tetrodotoxin (TTX) application to the soma blocked LTP in adults, but not juveniles. These data demonstrate that somatic spiking is more important for LTP induction in the adult as opposed to juvenile rats and we hypothesize that the basis for this is the ability of action potentials in the postsynaptic CA1 pyramidal neurone to back-propagate into the dendrites. Therefore, the pre- and postsynaptic activity patterns required to induce LTP mature as the hippocampus develops.
突触前和突触后活动的同时发生会在海马体CA1区锥体神经元的Schaffer侧支突触处诱导突触可塑性。目前尚不清楚诱导突触可塑性所需的精确时间、频率和同时发生的动作电位数量。在本研究中,我们表明诱导长时程增强(LTP)所需的突触后活动会随着发育而变化。在成年大鼠的急性脑片中,突触前和突触后同时进行的theta爆发刺激(TBS)可诱导LTP,并且我们发现需要多个高频突触后尖峰。相比之下,在幼年(P14)大鼠的急性脑片中,TBS未能诱导LTP,除非兴奋性突触后电位(EPSP)的幅度足以引发动作电位。我们还表明,当突触前和突触后单个动作电位以大于5Hz的频率发放时,仅在幼年时能够诱导LTP,并且突触前和突触后单个动作电位之间的相对时间并不重要。最后,我们表明向成年动物的胞体局部应用河豚毒素(TTX)可阻断LTP,但对幼年动物无效。这些数据表明,与幼年大鼠相比,成年大鼠中体细胞发放对于LTP诱导更为重要,我们推测其基础是突触后CA1锥体神经元中的动作电位能够反向传播到树突中。因此,诱导LTP所需的突触前和突触后活动模式会随着海马体的发育而成熟。