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低强度和高强度θ波模式刺激诱导和逆转长时程增强效应。

Induction and reversal of long-term potentiation by low- and high-intensity theta pattern stimulation.

作者信息

Barr D S, Lambert N A, Hoyt K L, Moore S D, Wilson W A

机构信息

Department of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Neurosci. 1995 Jul;15(7 Pt 2):5402-10. doi: 10.1523/JNEUROSCI.15-07-05402.1995.

Abstract

Reversal of long-term potentiation by low-frequency stimulation is often referred to as depotentiation. However, it is not clear whether depotentiation induced by low-frequency stimulation and long-term depression (LTD) induced by similar stimuli are distinct phenomena. We have performed a series of experiments in area CA1 of rat hippocampal slices in which a single pattern of theta-burst (TB) stimulation (Larson, et al., 1986; Staubli and Lynch, 1987) was found to produce either LTP or reversal of LTP depending on the intensity of the stimulation. TB stimulation (10 trains consisting of 4 pulses at 100 Hz, 200 msec apart) delivered at test pulse-intensity induced LTP. However, the same stimulation delivered at a higher intensity (10 times that of the test pulse, evoking a maximal response) did not induce LTP or depression of control responses, but produced lasting depression of previously potentiated responses. This reversal of LTP (TB depotentiation) was observed when the stimulus was delivered between 0.5 and 110 min after induction of LTP. TB depotentiation was reversible, cumulative and saturable when high-intensity TB trains were delivered in succession. TB depotentiation was also blocked by antagonists at NMDA receptors. Low-frequency (1 Hz) stimulation induced LTD, indicating that responses were not already maximally depressed. In addition, high-intensity TB stimulation did not reverse LTD. These results suggest that depotentiation induced by maximal TB stimulation and LTD induced by low-frequency stimulation are distinct phenomena, yet share some characteristics common to forms synaptic plasticity mediated by NMDA receptor activation.

摘要

低频刺激引起的长时程增强的反转通常被称为去增强作用。然而,低频刺激诱导的去增强作用与相似刺激诱导的长时程抑制(LTD)是否为不同现象尚不清楚。我们在大鼠海马切片的CA1区进行了一系列实验,其中发现单一模式的θ波爆发(TB)刺激(Larson等人,1986年;Staubli和Lynch,1987年)根据刺激强度可产生长时程增强(LTP)或LTP的反转。以测试脉冲强度给予的TB刺激(10串,每串由100 Hz的4个脉冲组成,间隔200毫秒)诱导了LTP。然而,以更高强度(测试脉冲强度的10倍,引发最大反应)给予相同刺激并未诱导LTP或对照反应的抑制,而是使先前增强的反应产生了持久的抑制。当在LTP诱导后0.5至110分钟之间给予刺激时,观察到了这种LTP的反转(TB去增强作用)。当连续给予高强度TB串时,TB去增强作用是可逆的、累积的且可饱和的。TB去增强作用也被NMDA受体拮抗剂所阻断。低频(1 Hz)刺激诱导了LTD,表明反应尚未被最大程度地抑制。此外,高强度TB刺激并未反转LTD。这些结果表明,最大TB刺激诱导的去增强作用和低频刺激诱导的LTD是不同的现象,但具有一些由NMDA受体激活介导的突触可塑性形式所共有的特征。

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