Woodin Melanie A, Ganguly Karunesh, Poo Mu-ming
Division of Neurobiology, Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Neuron. 2003 Aug 28;39(5):807-20. doi: 10.1016/s0896-6273(03)00507-5.
Coincident pre- and postsynaptic activation is known to induce long-term modification of glutamatergic synapses. We report here that, in both hippocampal cultures and acute hippocampal slices, repetitive postsynaptic spiking within 20 ms before and after the activation of GABAergic synapses also led to a persistent change in synaptic strength. This synaptic modification required Ca2+ influx through postsynaptic L-type Ca2+ channels and was due to a local decrease in K+-Cl- cotransport activity, effectively reducing the strength of inhibition. Thus, GABAergic synapses can detect and be modified by coincident pre- and postsynaptic spiking, allowing the level of inhibition to be modulated in accordance to the temporal pattern of postsynaptic excitation.
已知突触前和突触后同时激活可诱导谷氨酸能突触的长期修饰。我们在此报告,在海马体培养物和急性海马体切片中,在GABA能突触激活之前和之后20毫秒内的重复性突触后放电也会导致突触强度的持续变化。这种突触修饰需要Ca2+通过突触后L型Ca2+通道内流,并且是由于K+-Cl-共转运活性的局部降低,有效地降低了抑制强度。因此,GABA能突触可以通过突触前和突触后同时放电来检测并被修饰,从而使抑制水平能够根据突触后兴奋的时间模式进行调节。