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首页> 外文期刊>Frontiers in Cellular Neuroscience >Ontogeny of kainate-induced gamma oscillations in the rat CA3 hippocampus in vitro
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Ontogeny of kainate-induced gamma oscillations in the rat CA3 hippocampus in vitro

机译:红藻氨酸诱导的大鼠CA3海马体γ振荡的个体发育体外

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GABAergic inhibition, which is instrumental in the generation of hippocampal gamma oscillations, undergoes significant changes during development. However, the development of hippocampal gamma oscillations remains largely unknown. Here, we explored the developmental features of kainate-induced oscillations (KA-Os) in CA3 region of rat hippocampal slices. Up to postnatal day P5, the bath application of kainate failed to evoke any detectable oscillations. KA-Os emerged by the end of the first postnatal week; these were initially weak, slow (20–25 Hz, beta range) and were poorly synchronized with CA3 units and synaptic currents. Local field potential (LFP) power, synchronization of units and frequency of KA-Os increased during the second postnatal week to attain gamma (30–40 Hz) frequency by P15–21. Both beta and gamma KA-Os are characterized by alternating sinks and sources in the pyramidal cell layer, likely generated by summation of the action potential—associated currents and GABAergic synaptic currents, respectively. Blockade of GABA(A) receptors with gabazine completely suppressed KA-Os at all ages indicating that GABAergic mechanisms are instrumental in their generation. Bumetanide, a NKCC1 chloride co-transporter antagonist which renders GABAergic responses inhibitory in the immature hippocampal neurons, failed to induce KA-Os at P2–4 indicating that the absence of KA-Os in neonates is not due to depolarizing actions of GABA. The linear developmental profile, electrographic features and pharmacological properties indicate that CA3 hippocampal beta and gamma KA-Os are fundamentally similar in their generative mechanisms and their delayed onset and developmental changes likely reflect the development of perisomatic GABAergic inhibition.
机译:GABA能抑制在海马伽马振荡的产生中起重要作用,在发育过程中发生了显着变化。然而,海马伽马振荡的发展仍然很大程度上未知。在这里,我们探讨了大鼠海马切片CA3区的海藻酸盐诱导的振荡(KA-Os)的发育特征。直到出生后第5天,海藻酸盐的沐浴应用未能引起任何可检测到的振荡。产后第一个星期结束时出现了KA-Os。这些最初很弱,很慢(20-25 Hz,β范围),并且与CA3单位和突触电流同步性很差。在产后第二周,局部场势(LFP)功率,单位同步和KA-O频率增加,到P15-21时达到γ(30-40 Hz)频率。 β和γ-KA-Os的特征都在于锥体细胞层中的汇和源交替发生,这很可能是由动作电位的总和所产生的,分别是相关电流和GABA能突触电流。在所有年龄段中,用gabazine阻断GABA(A)受体都能完全抑制KA-O,这表明GABA能机制在其生成过程中发挥了重要作用。布美他尼是一种能抑制未成熟海马神经元中GABA能反应的NKCC1氯化物共转运拮抗剂,未能在P2-4诱导KA-O,这表明新生儿中KA-O的缺乏并非归因于GABA的去极化作用。线性发育概况,电子照相特征和药理特性表明,CA3海马β和γKA-Os的生成机理基本相似,其延迟的发作和发育变化可能反映了过时的GABA能抑制作用的发展。

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