Anaesthetic/amnesic agents disrupt beta frequency oscillations associated with potentiation of excitatory synaptic potentials in the rat hippocampal slice

被引:57
作者
Faulkner, HJ
Traub, RD
Whittington, MA
机构
[1] Univ London Imperial Coll Sci Technol & Med, Cellular & Integrat Biol Sect, London SW7 2AZ, England
[2] Univ Birmingham, Sch Med, Div Neurosci, Birmingham B15 2TT, W Midlands, England
[3] Univ Leeds, Sch Biomed Sci, Leeds LS2 9NL, W Yorkshire, England
基金
英国惠康基金;
关键词
anaesthetic; gamma oscillation; synchrony; beta oscillation; synaptic potentiation; memory;
D O I
10.1038/sj.bjp.0702948
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Anaesthetic agents produce disruption in cognitive function typified by reductions in sensory perception and memory formation. Oscillations within the EEG gamma and beta bands have been linked to sensory perception and memory and have been shown to be modified by anaesthetic agents. 2 Synchronous gamma oscillations generated by brief tetanic stimulation in two regions of hippocampal area CA1 in slices in vitro were seen to potentiate excitatory synaptic communication between the areas. This synaptic potentiation, was seen to contribute to a transition from gamma frequency (30-70 Hz) to beta frequency (12-30 Hz) oscillations. 3 Four drugs having anaesthetic/hypnotic and amnesic properties were tested on this synchronous gamma-induced beta oscillation. Thiopental 10-200 mu M, Diazepam 0.05-1.0 mu M, Morphine 10-200 mu M, and Ketamine 10-200 mu M were all added to the bathing medium. Each drug markedly disrupted the formation of beta oscillations in a manner consistent with their primary modes of action. Thiopental and morphine disrupted synchrony of gamma oscillations and prevented potentiation of recurrent excitatory potentials measured in stratum oriens (fEPSPs). Neither diazepam, nor ketamine produced such marked changes in synchrony at gamma frequencies or reduction in potentiation of fEPSPs. However, each disrupted expression of subsequent beta oscillation via changes in the magnitude of inhibitory network gamma oscillations and the duration and magnitude of tetanus-induced depolarization respectively. 4 The degree of disruption of fEPSP potentiation correlated quantitatively with the degree of disruption in synchrony between sites during gamma oscillations. The data indicate that synchronous gamma-induced beta oscillations represent a mode of expression of excitatory synaptic potentiation in the hippocampus, and that anaesthetic/amnesic agents can disrupt this process markedly.
引用
收藏
页码:1813 / 1825
页数:13
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