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J Physiol Volume 521, Number 3, 629-636, December 15, 1999
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The Journal of Physiology (1999), 521.3, pp. 629-636
© Copyright 1999 The Physiological Society

Direct demonstration of persistent Na+ channel activity in dendritic processes of mammalian cortical neurones

Jacopo Magistretti *¹, David S. Ragsdale * and Angel Alonso *

* Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, 3801 University Street, Montréal, Québec, Canada H3A 2B4 and ¹ Laboratorio di Biofisica e Neurofisiologia dei Sistemi Corticali, Dipartimento di Neurofisiologia Sperimentale, Istituto Nazionale Neurologico 'Carlo Besta', Via Celoria 11, 20133 Milano, Italy

  1. Single Na+ channel activity was recorded in patch-clamp, cell-attached experiments performed on dendritic processes of acutely isolated principal neurones from rat entorhinal-cortex layer II. The distances of the recording sites from the soma ranged from ~20 to ~100 µm.

  2. Step depolarisations from holding potentials of -120 to -100 mV to test potentials of -60 to +10 mV elicited Na+ channel openings in all of the recorded patches (n = 16).

  3. In 10 patches, besides transient Na+ channel openings clustered within the first few milliseconds of the depolarising pulses, prolonged and/or late Na+ channel openings were also regularly observed. This 'persistent' Na+ channel activity produced net inward, persistent currents in ensemble-average traces, and remained stable over the entire duration of the experiments (~9 to 30 min).

  4. Two of these patches contained <= 3 channels. In these cases, persistent Na+ channel openings could be attributed to the activity of one single channel.

  5. The voltage dependence of persistent-current amplitude in ensemble-average traces closely resembled that of whole-cell, persistent Na+ current expressed by the same neurones, and displayed the same characteristic low threshold of activation.

  6. Dendritic, persistent Na+ channel openings had relatively high single-channel conductance (~20 pS), similar to what is observed for somatic, persistent Na+ channels.

  7. We conclude that a stable, persistent Na+ channel activity is expressed by proximal dendrites of entorhinal-cortex layer II principal neurones, and can contribute a significant low-threshold, persistent Na+ current to the dendritic processing of excitatory synaptic inputs.



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