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大鼠海马体中突触反应的长期增强和抑制:定位与频率依赖性

Long-term potentiation and depression of synaptic responses in the rat hippocampus: localization and frequency dependency.

作者信息

Dunwiddie T, Lynch G

出版信息

J Physiol. 1978 Mar;276:353-67. doi: 10.1113/jphysiol.1978.sp012239.

DOI:10.1113/jphysiol.1978.sp012239
PMID:650459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1282430/
Abstract
  1. The consequences of repetitive activation of excitatory synaptic inputs to the CA1 pyramidal cells of rat hippocampus have been studied using in vitro techniques. 2. Single stimulation trains of 100 pulses at rates of 5-100/sec resulted in potentiation of population spike amplitudes lasting the duration of a 5 min test period in thirty-four out of thirty-five cases. Trains of 100 pulses delivered at 1/sec resulted in depression of the stimulated pathway in ten out of twelve experiments. 3. Responses to test stimulation of other excitatory inputs to the same cell population were depressed following conditioning trains at frequencies in the range 1-100/sec. Depression was seen both in the population spike amplitude (reflecting synchronous cell discharge) as well as the extracellularly recorded population e.p.s.p., and appeared to be maximal at lower frequencies. 4. Trains of antidromic stimulation of the CA1 cell population produced subsequent decreases in synaptically evoked responses, indicating that repetitive firing of pyramidal neurones or interneurones do not cause potentiation, but may be involved in heterosynaptic depression. 5. The results suggest that potentiation and heterosynaptic depression arise from different mechanisms, and that potentiation is confined to the set of terminals activated by a conditioning train, whereas the depression is generalized to the whole neurone.
摘要
  1. 利用体外技术研究了对大鼠海马CA1锥体神经元兴奋性突触输入进行重复激活的后果。2. 以5 - 100次/秒的频率进行100个脉冲的单次刺激串,在35个案例中的34个中,群体峰电位幅度在5分钟测试期内持续增强。以1次/秒的频率给予100个脉冲的刺激串,在12个实验中的10个中导致受刺激通路的抑制。3. 在1 - 100次/秒的频率范围内进行条件刺激串后,对同一细胞群体其他兴奋性输入的测试刺激反应受到抑制。群体峰电位幅度(反映同步细胞放电)以及细胞外记录的群体兴奋性突触后电位均出现抑制,且在较低频率时似乎最为明显。4. 对CA1细胞群体进行逆向刺激串后,突触诱发反应随后降低,这表明锥体神经元或中间神经元的重复放电不会引起增强,而是可能参与异突触抑制。5. 结果表明,增强和异突触抑制源于不同机制,增强局限于由条件刺激串激活的终末集合,而抑制则扩展至整个神经元。

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