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The Journal of Neurophysiology Vol. 84 No. 1 July 2000, pp. 390-400
Copyright ©2000 by the American Physiological Society
Center for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark, New Jersey 07102
Henze, Darrell A.,
Zsolt Borhegyi,
Jozsef Csicsvari,
Akira Mamiya,
Kenneth D. Harris, and
György Buzsáki.
Intracellular Features Predicted by Extracellular Recordings in
the Hippocampus In Vivo. J. Neurophysiol. 84: 390-400, 2000. Multichannel tetrode array recording in
awake behaving animals provides a powerful method to record the
activity of large numbers of neurons. The power of this method could be
extended if further information concerning the intracellular state of
the neurons could be extracted from the extracellularly recorded
signals. Toward this end, we have simultaneously recorded intracellular and extracellular signals from hippocampal CA1 pyramidal cells and
interneurons in the anesthetized rat. We found that several intracellular parameters can be deduced from extracellular spike waveforms. The width of the intracellular action potential is defined
precisely by distinct points on the extracellular spike. Amplitude
changes of the intracellular action potential are reflected by changes
in the amplitude of the initial negative phase of the extracellular
spike, and these amplitude changes are dependent on the state of the
network. In addition, intracellular recordings from dendrites with
simultaneous extracellular recordings from the soma indicate that, on
average, action potentials are initiated in the perisomatic region and
propagate to the dendrites at 1.68 m/s. Finally we determined that a
tetrode in hippocampal area CA1 theoretically should be able to record
electrical signals from ~1,000 neurons. Of these, 60-100 neurons
should generate spikes of sufficient amplitude to be detectable from
the noise and to allow for their separation using current spatial
clustering methods. This theoretical maximum is in contrast to the
approximately six units that are usually detected per tetrode. From
this, we conclude that a large percentage of hippocampal CA1 pyramidal cells are silent in any given behavioral condition.
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