Recruitment of Perisomatic Inhibition during Spontaneous Hippocampal Activity In Vitro

被引:13
作者
Beyeler, Anna [1 ,2 ,3 ]
Retailleau, Aude [1 ,2 ,3 ]
Molter, Colin [1 ,2 ,3 ]
Mehidi, Amine [1 ,2 ,3 ]
Szabadics, Janos [4 ]
Leinekugel, Xavier [1 ,2 ,3 ]
机构
[1] Univ Bordeaux, Inst Malad Neurodegenerat, UMR 5293, Bordeaux, France
[2] Inst Malad Neurodegenerat, CNRS, UMR 5293, Bordeaux, France
[3] European Network Inst, Bordeaux, France
[4] Hungarian Acad Sci, Inst Expt Med, Budapest, Hungary
基金
英国惠康基金;
关键词
GUINEA-PIG HIPPOCAMPUS; INTERNEURON DIVERSITY SERIES; PYRAMIDAL CELLS; RAT HIPPOCAMPUS; NETWORK OSCILLATIONS; SYNAPTIC PLASTICITY; NEURONS; MEMORY; POTENTIALS; CIRCUITS;
D O I
10.1371/journal.pone.0066509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It was recently shown that perisomatic GABAergic inhibitory postsynaptic potentials (IPSPs) originating from basket and chandelier cells can be recorded as population IPSPs from the hippocampal pyramidal layer using extracellular electrodes (eIPSPs). Taking advantage of this approach, we have investigated the recruitment of perisomatic inhibition during spontaneous hippocampal activity in vitro. Combining intracellular and extracellular recordings from pyramidal cells and interneurons, we confirm that inhibitory signals generated by basket cells can be recorded extracellularly, but our results suggest that, during spontaneous activity, eIPSPs are mostly confined to the CA3 rather than CA1 region. CA3 eIPSPs produced the powerful time-locked inhibition of multi-unit activity expected from perisomatic inhibition. Analysis of the temporal dynamics of spike discharges relative to eIPSPs suggests significant but moderate recruitment of excitatory and inhibitory neurons within the CA3 network on a 10 ms time scale, within which neurons recruit each other through recurrent collaterals and trigger powerful feedback inhibition. Such quantified parameters of neuronal interactions in the hippocampal network may serve as a basis for future characterisation of pathological conditions potentially affecting the interactions between excitation and inhibition in this circuit.
引用
收藏
页数:11
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