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J Neurophysiol 94: 741-753, 2005. First published March 16, 2005; doi:10.1152/jn.00086.2005
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An In Vitro Model of Hippocampal Sharp Waves: Regional Initiation and Intracellular Correlates

Chiping Wu1,5, Marjan Nassiri Asl1,5, Jesse Gillis1,3, Frances K. Skinner1,2,3,4,5 and Liang Zhang1,2,5

1Toronto Western Research Institute, University Health Network, Department of Medicine, 2Division of Neurology, 3Department of Physiology, 4Institute of Biomaterials and Biomedical Engineering, and 5Epilepsy Research Program, University of Toronto, Toronto, Ontario, Canada

Submitted 24 January 2005; accepted in final form 14 March 2005

During slow wave sleep and consummatory behaviors, electroencephalographic recordings from the rodent hippocampus reveal large amplitude potentials called sharp waves. The sharp waves originate from the CA3 circuitry and their generation is correlated with coherent discharges of CA3 pyramidal neurons and dependent on activities mediated by AMPA glutamate receptors. To model sharp waves in a relatively large hippocampal circuitry in vitro, we developed thick (1 mm) mouse hippocampal slices by separating the dentate gyrus from the CA2/CA1 areas while keeping the functional dentate gyrus-CA3-CA1 connections. We found that large amplitude (0.3–3 mV) sharp wave-like field potentials occurred spontaneously in the thick slices without extra ionic or pharmacological manipulation and they resemble closely electroencephalographic sharp waves with respect to waveform, regional initiation, pharmacological manipulations, and intracellular correlates. Through measuring tissue O2, K+, and synaptic and single cell activities, we verified that the sharp wave-like potentials are not a consequence of anoxia, nonspecific elevation of extracellular K+ and dissection-related tissue damage. Our data suggest that a subtle but crucial increase in the CA3 glutamatergic activity effectively recruits a population of neurons thus responsible for the generation of the sharp wave-like spontaneous field potentials in isolated hippocampal circuitry.


Address for reprint requests and other correspondence: L. Zhang, Div. of Cellular and Molecular Biology, Toronto Western Research Inst., Rm. 13-411, Toronto Western Hospital, 399 Bathurst St., Toronto, Ontario M5T 2S8, Canada (E-mail: liangz{at}uhnres.utoronto.ca)




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