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海马体CA1区输入特异性非NMDA受体依赖性长时程增强对NMDA受体的依赖性

NMDA receptor dependence of the input specific NMDA receptor-independent LTP in the hippocampal CA1 region.

作者信息

Pananceau M, Gustafsson B

机构信息

Department of Physiology and Pharmacology, Göteborg University, Sweden.

出版信息

Brain Res. 1997 Mar 28;752(1-2):255-60. doi: 10.1016/s0006-8993(96)01471-0.

Abstract

An important characteristic of long-term potentiation (LTP) in the hippocampal CA1 region is that it is specific for those synapses which are active during the induction event. This input specificity is commonly attributed to the location and properties of the N-methyl-D-aspartate (NMDA) receptor channel. Experiments using strong high-frequency orthodromic activation have suggested that input-specific LTP can occur also in the absence of NMDA receptor activation. The present experiments have re-examined this question. They were performed in the CA1 region of hippocampal slices, and the synaptic strength was evaluated from the initial slope of the dendritically recorded field potential. In agreement with previous reports, 0.5 s, 200 Hz, orthodromic trains were found to lead to a substantial input-specific LTP (averaging 62%) in the presence of the competitive NMDA receptor antagonist D-(-)-2-amino-5-phosphonopentanoic acid (D-AP5) (20 microM). Under conditions of higher NMDA receptor blockade considerably less LTP was evoked. In 50 microM D-AP5 and 20 microM chloro-kynurenate LTP averaged 13.4%, and after addition of 20 microM (+)-dizicilpine maleate (MK-801) LTP averaged 5.9%. On the other hand, in 20 microM D-AP5 and 20 microM of the calcium channel antagonist nifedipine LTP averaged 49.9%. The present results suggest that NMDA receptor activity remaining in high concentrations of AP5 is sufficient to underly LTP induction under strong induction conditions.

摘要

海马体CA1区长期增强(LTP)的一个重要特征是,它对在诱导事件中活跃的那些突触具有特异性。这种输入特异性通常归因于N-甲基-D-天冬氨酸(NMDA)受体通道的位置和特性。使用强高频顺向激活的实验表明,在没有NMDA受体激活的情况下也可能发生输入特异性LTP。本实验重新审视了这个问题。实验在海马切片的CA1区进行,通过树突记录的场电位的初始斜率评估突触强度。与之前的报道一致,发现在存在竞争性NMDA受体拮抗剂D-(-)-2-氨基-5-磷酸戊酸(D-AP5)(20微摩尔)的情况下,0.5秒、200赫兹的顺向电刺激序列会导致大量的输入特异性LTP(平均为62%)。在更高的NMDA受体阻断条件下,诱发的LTP要少得多。在50微摩尔D-AP5和20微摩尔氯犬尿氨酸存在的情况下,LTP平均为13.4%,添加20微摩尔(+)-马来酸二氮嗪(MK-801)后,LTP平均为5.9%。另一方面,在20微摩尔D-AP5和20微摩尔钙通道拮抗剂硝苯地平存在的情况下,LTP平均为49.9%。目前的结果表明,在高浓度AP5中残留的NMDA受体活性足以在强诱导条件下引发LTP诱导。

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