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大鼠海马-内嗅皮层联合脑片中穿通通路向海马CA1区的投射

The perforant path projection to hippocampal area CA1 in the rat hippocampal-entorhinal cortex combined slice.

作者信息

Empson R M, Heinemann U

机构信息

Department of Neurophysiology, Institute for Physiology at the Charité, Humboldt Universität Berlin, Germany.

出版信息

J Physiol. 1995 May 1;484 ( Pt 3)(Pt 3):707-20. doi: 10.1113/jphysiol.1995.sp020697.

Abstract
  1. The perforant path projection from layer III of the entorhinal cortex to CA1 of the hippocampus was studied within a hippocampal-entorhinal combined slice preparation. We prevented contamination from the other main hippocampal pathways by removal of CA3 and the dentate gyrus. 2. Initially the projection was mapped using field potential recordings that suggested an excitatory sink in stratum lacunosum moleculare with an associated source in stratum pyramidale. 3. However, recording intracellularly from CA1 cells, stimulation of the perforant path produced prominent fast GABAA and slow GABAB IPSPs often preceded by small EPSPs. In a small number of cells we observed EPSPs only. 4. CNQX blocked excitatory and inhibitory responses. This indicated the presence of an intervening excitatory synapse between the inhibitory interneurone and the pyramidal cell. 5. Focal bicuculline applications revealed that the major site of GABAA inhibitory input was to stratum radiatum of CA1. 6. The inhibition activated by the perforant path was very effective at reducing simultaneously activated Schaffer collateral mediated EPSPs and suprathreshold-stimulated action potentials. 7. Blockade of fast inhibition increased excitability and enhanced slow inhibition. Both increases relied upon the activation of NMDA receptors. 8. Perforant path inputs activated prominent and effective disynaptic inhibition of CA1 cells. This has significance for the output of hippocampal processing during normal behaviour and also under pathological conditions.
摘要
  1. 在海马-内嗅联合脑片制备中,研究了从内嗅皮质第III层到海马CA1区的穿通通路投射。我们通过去除CA3和齿状回,防止了来自其他主要海马通路的污染。2. 最初,使用场电位记录对该投射进行了定位,结果表明在分子层隙状层有一个兴奋性汇,在锥体细胞层有一个相关的源。3. 然而,在CA1细胞内记录时,刺激穿通通路会产生明显的快速GABAA和缓慢的GABAB抑制性突触后电位,通常在小的兴奋性突触后电位之前出现。在少数细胞中,我们只观察到兴奋性突触后电位。4. CNQX阻断了兴奋性和抑制性反应。这表明在抑制性中间神经元和锥体细胞之间存在一个中间兴奋性突触。5. 局部应用荷包牡丹碱显示,GABAA抑制性输入的主要部位是CA1区的辐射层。6. 穿通通路激活的抑制作用在减少同时激活的Schaffer侧支介导的兴奋性突触后电位和阈上刺激动作电位方面非常有效。7. 快速抑制的阻断增加了兴奋性并增强了缓慢抑制。这两种增加都依赖于NMDA受体的激活。8. 穿通通路输入激活了对CA1细胞的显著且有效的双突触抑制。这对于正常行为期间以及病理条件下海马处理的输出具有重要意义。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d026/1157954/2aea7dcc6c8e/jphysiol00324-0178-a.jpg

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