Whole cell recordings from CA1 pyramidal cells were performed to investigate the interaction between excitatory postsynaptic potentials (EPSPs) or currents (EPSCs), and the slow Ca(2+)-dependent K(+) current, I(sAHP). Blockers of the slow afterhyperpolarization (sAHP) such as isoprenaline (ISO) or noradrenaline (NA) reduced the hyperpolarization that followed a short train of EPSPs, and slowed the decay of summated EPSPs or EPSCs. 2. ISO/NA action on synaptic responses was observed in the absence of action potentials, but was curtailed by Ca(2+) chelation (10 mM EGTA in the electrode) and was not observed with a caesium-based recording solution. This suggests the involvement of an ISO/NA-sensitive Ca(2+)-dependent K(+) current without a requirement for regenerative spiking. 3. An ISO/NA-sensitive sAHP was observed following both NMDA and non-NMDA receptor-mediated EPSP trains in nominally zero Mg(2+) medium. Isoprenaline sensitivity was blocked by hyperpolarization during EPSPs or by isradipine, suggesting a requirement for voltage-dependent Ca(2+) influx during EPSPs. The data indicate that bursts of EPSPs can activate voltage-gated Ca(2+) channels, which trigger I(sAHP) during synaptic responses. 4. A decrease in EPSP temporal summation occurred during both spike-evoked sAHPs and persistent activation of sAHP conductance following internal dialysis with diazo-2 (2 mM). At constant membrane potential, diazo-2 caused a decrease in membrane time constant and input resistance and accelerated the rate of EPSP decay. Photolysis of diazo-2 or application of NA reduced the resting sAHP conductance, causing an increased membrane time constant and input resistance in association with an increase in EPSP half-width. 5. These results indicate that short bursts of EPSPs can activate a Ca(2+)-dependent K(+) current resembling I(sAHP), and that activation of this current reduces the postsynaptic response to high-frequency synaptic input. The findings imply that modulation of I(sAHP) can regulate synaptic efficacy and may influence the threshold for tetanus-induced synaptic plasticity.
摘要
对CA1锥体细胞进行全细胞记录,以研究兴奋性突触后电位(EPSP)或电流(EPSC)与缓慢的钙依赖性钾电流I(sAHP)之间的相互作用。异丙肾上腺素(ISO)或去甲肾上腺素(NA)等缓慢超极化后电位(sAHP)阻滞剂可减少短串EPSP后的超极化,并减缓总和EPSP或EPSC的衰减。2. 在无动作电位的情况下观察到ISO/NA对突触反应的作用,但被钙螯合(电极中10 mM EGTA)所抑制,且在基于铯的记录溶液中未观察到。这表明存在一种对ISO/NA敏感的钙依赖性钾电流,且无需再生性动作电位。3. 在名义上零镁(2+)培养基中,NMDA和非NMDA受体介导的EPSP串后均观察到对ISO/NA敏感的sAHP。EPSP期间的超极化或异搏定可阻断异丙肾上腺素敏感性,提示EPSP期间需要电压依赖性钙内流。数据表明,EPSP爆发可激活电压门控钙通道,在突触反应期间触发I(sAHP)。4. 在用重氮-2(2 mM)进行细胞内透析后,在动作电位诱发的sAHP和sAHP电导的持续激活过程中,EPSP时间总和均减少。在恒定膜电位下,重氮-2导致膜时间常数和输入电阻降低,并加速EPSP衰减。重氮-2的光解或NA的应用降低了静息sAHP电导,导致膜时间常数和输入电阻增加,同时EPSP半宽度增加。5. 这些结果表明,短串EPSP可激活类似于I(sAHP)的钙依赖性钾电流,且该电流的激活会降低突触后对高频突触输入的反应。这些发现意味着I(sAHP) 的调节可调控突触效能,并可能影响破伤风诱导的突触可塑性阈值。