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成年自由活动大鼠新皮层中的长时程增强。

Long-term potentiation in the neocortex of the adult, freely moving rat.

作者信息

Trepel C, Racine R J

机构信息

Department of Psychology, McMaster University, Hamilton, Ontario, Canada.

出版信息

Cereb Cortex. 1998 Dec;8(8):719-29. doi: 10.1093/cercor/8.8.719.

Abstract

Neocortical preparations have proven highly resistant to the induction of long-term potentiation (LTP), and we have only recently determined the conditions sufficient for the induction of neocortical LTP in the adult, freely moving rat. The stimulation trains must be spaced and repeated over a period of days in order to reach asymptotic levels of potentiation. Here we show that, within these constraints, the neocortex is actually highly responsive. LTP could be induced with as few as one brief high frequency train per day or with extremely low-intensity stimulation trains. We also provide evidence for a critical role for N-methyl-D-aspartate (NMDA) receptor activation in LTP induction in this preparation, and demonstrate that this LTP is input-specific. Control pathways showed no potentiation effects. LTP was found in a monosynaptic and two polysynaptic components (average latencies to peak: 8.1, 15.2 and 20.0 ms) and in the superimposed population spikes. Although LTP could be induced with one train per day or with low-intensity trains, larger and longer-lasting potentiation effects could be induced by increasing the number of trains delivered per session, the number of sessions over which trains were delivered, or the pulse intensity of the trains. The LTP decayed slowly and was still evident 5 weeks later. Administration of the competitive NMDA antagonist 3-[(+/-)-2-carboxypiperazin-4-yl]-propyl-1-phosphonic acid blocked the induction of LTP in a dose-dependent fashion and appeared to unmask a depression of both the population spikes and a polysynaptic component. These results indicate that the neocortex is highly sensitive to LTP induction procedures, as long as the stimulation trains are spaced and applied over a period of days. They are also consistent with the view that the neocortex must operate with a slow learning rate to reduce interference effects in memory.

摘要

新皮质制剂已被证明对长时程增强(LTP)的诱导具有高度抗性,直到最近我们才确定了在成年自由活动大鼠中诱导新皮质LTP的充分条件。刺激序列必须在数天内间隔并重复,以达到增强的渐近水平。在这里我们表明,在这些限制条件下,新皮质实际上具有高度的反应性。每天只需一次短暂的高频序列或极低强度的刺激序列就能诱导LTP。我们还提供证据表明N-甲基-D-天冬氨酸(NMDA)受体激活在该制剂的LTP诱导中起关键作用,并证明这种LTP是输入特异性的。对照通路没有增强效应。在单突触和两个多突触成分中发现了LTP(峰值平均潜伏期:8.1、15.2和20.0毫秒)以及叠加的群体峰电位中。尽管每天一次序列或低强度序列就能诱导LTP,但通过增加每次会话传递的序列数量、传递序列的会话数量或序列的脉冲强度,可以诱导出更大且持续时间更长的增强效应。LTP衰减缓慢,5周后仍很明显。竞争性NMDA拮抗剂3-[(+/-)-2-羧基哌嗪-4-基]-丙基-1-膦酸以剂量依赖的方式阻断了LTP的诱导,并且似乎揭示了群体峰电位和一个多突触成分的抑制。这些结果表明,只要刺激序列间隔并在数天内施加,新皮质对LTP诱导程序高度敏感。它们也与新皮质必须以缓慢的学习速率运作以减少记忆中的干扰效应这一观点一致。

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