Xu Chun, Zhao Man-xia, Poo Mu-ming, Zhang Xiao-hui
Institute of Neuroscience, State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road Shanghai 200031, China.
Nat Neurosci. 2008 Dec;11(12):1410-8. doi: 10.1038/nn.2215. Epub 2008 Oct 26.
Activity-induced long-term modification of glutamatergic synapses depends on the frequency of synaptic activation. We found that long-term modification of developing rat hippocampal GABAergic synapses that was induced by repetitive coincident pre- and postsynaptic spiking was also frequency dependent. Spiking at 20-50 Hz resulted in synaptic potentiation, whereas spiking at 5 Hz led to synaptic depression. The potentiation was abolished by blocking GABA(B) receptors (GABA(B)Rs), whereas the depression was independent of GABA(B)R activation and could be converted to potentiation by elevating GABA(B)R activity. The potentiation could be attributed to a local postsynaptic increase in Na(+)/K(+)/2Cl(-) co-transporter activity near activated synapses. The activity of postsynaptic Ca(2+)/calmodulin-dependent protein kinase II was necessary for long-term potentiation of these developing GABAergic synapses and its phosphorylation at Thr286 could be enhanced by activating GABA(B)Rs with baclofen. Together with our finding that activation of GABA(B)Rs is frequency dependent, these results indicate that postsynaptic GABA(B)R activation mediates frequency-dependent potentiation of developing GABAergic synapses.
由活动诱导的谷氨酸能突触的长期修饰取决于突触激活的频率。我们发现,发育中大鼠海马GABA能突触由重复的突触前和突触后同步放电诱导的长期修饰也是频率依赖性的。20 - 50Hz的放电导致突触增强,而5Hz的放电则导致突触抑制。通过阻断GABA(B)受体(GABA(B)Rs)可消除增强作用,而抑制作用独立于GABA(B)R激活,并且通过提高GABA(B)R活性可将其转变为增强作用。增强作用可归因于激活突触附近局部突触后Na(+)/K(+)/2Cl(-)共转运体活性增加。突触后Ca(2+)/钙调蛋白依赖性蛋白激酶II的活性对于这些发育中的GABA能突触的长期增强是必需的,并且用巴氯芬激活GABA(B)Rs可增强其在苏氨酸286位点的磷酸化。连同我们发现GABA(B)R激活是频率依赖性的这一结果,这些结果表明突触后GABA(B)R激活介导发育中GABA能突触的频率依赖性增强。