Institute of Neuroscience and State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Science, Shanghai 200031, China.
J Neurosci. 2011 Mar 2;31(9):3328-35. doi: 10.1523/JNEUROSCI.5936-10.2011.
Spaced patterns of repetitive synaptic activation often result in a long-lasting, protein synthesis-dependent potentiation of synaptic transmission, known as late-phase long-term potentiation (L-LTP) that may serve as a substrate for long-term memory. Behavioral studies showed that posttraining blockade of NMDA subtype of the glutamate receptor (NMDAR) impaired long-term memory, although NMDAR activation is generally known to be required during LTP induction. In this study, we found that the establishment of L-LTP in vivo requires NMDAR activation within a critical time window after LTP induction. In the developing visual system of Xenopus laevis tadpole, L-LTP of retinotectal synapses could be induced by three episodes of theta burst stimulation (TBS) of the optic nerve with 5 min spacing ("spaced TBS"), but not by three TBS episodes applied en masse or spaced with intervals ≥10 min. Within a time window of ∼30 min after the spaced TBS, local perfusion of the tectum with NMDAR antagonist d-AP5 or Ca(2+)-chelator EGTA-AM impaired the establishment of L-LTP, indicating the requirement of postinduction activation of NMDAR/Ca(2+) signaling. Moreover, inhibiting spontaneous spiking activity in the tectum by local application of tetrodotoxin (TTX) prevented L-LTP when TTX was applied for 15 min immediately after the spaced TBS but not 1 h later, whereas the same postinduction TTX application in the retina had no effect. These findings offer new insights into the synaptic basis for the requirement of postlearning activation of NMDARs and point to the importance of postlearning spontaneous circuit activity in memory formation.
空间模式的重复突触激活通常会导致突触传递的长期、蛋白质合成依赖性增强,称为晚期长时程增强(L-LTP),它可能作为长期记忆的基础。行为研究表明,训练后阻断谷氨酸受体 NMDA 亚型(NMDAR)会损害长期记忆,尽管一般认为 NMDAR 激活是 LTP 诱导所必需的。在这项研究中,我们发现体内 L-LTP 的建立需要在 LTP 诱导后关键时间窗口内激活 NMDAR。在非洲爪蟾幼体的发育视觉系统中,通过视神经的三个θ爆发刺激(TBS)以 5 分钟的间隔(“间隔 TBS”)可以诱导视网膜-视顶盖突触的 L-LTP,但不能通过三个 TBS 以连续或间隔时间≥10 分钟的方式诱导。在间隔 TBS 后约 30 分钟的时间窗口内,用 NMDAR 拮抗剂 d-AP5 或 Ca(2+)螯合剂 EGTA-AM 局部灌注视顶盖会损害 L-LTP 的建立,表明诱导后 NMDAR/Ca(2+)信号的激活是必需的。此外,通过局部应用河豚毒素(TTX)抑制视顶盖中的自发尖峰活动,当 TTX 在间隔 TBS 后立即应用 15 分钟而不是 1 小时后应用时,可防止 L-LTP,但在视网膜中进行相同的诱导后 TTX 应用则没有影响。这些发现为学习后 NMDA 受体激活的突触基础提供了新的见解,并指出学习后自发电路活动在记忆形成中的重要性。