|
|
||||||||
Journal of Neurophysiology, Vol 64, Issue 5 1429-1441, Copyright © 1990 by APS
ARTICLES |
O. Herreras
Division of Physiology, Duke University Medical Center, Durham, North Carolina 27710.
1. The events leading to the Schaffer collateral-induced discharge of CA1 pyramidal neurons were investigated in the hippocampus of anesthetized rats by current source-density (CSD) analysis. 2. The earliest evoked currents detected shortly after a stimulus were a sink in the zone where synapses are known to be located (300-350 microns ventral to the somatic layer) flanked by two smaller sources in the distal portion of the apical dendrites and in the somatic layer. This synaptic sink (SyS) extended over 75-100 microns; it lasted for 15-20 ms, and it reached its maximum amplitude some milliseconds after the population spike (PS) and remained in the same location. Stimuli submaximal and supramaximal for evoking a PS yielded the same pattern of current distribution for the SyS. Presynaptic fiber volleys were not detected in these recordings. 3. During the rising phase of the SyS a second sink appeared in a more proximal portion of the apical dendrites. This late dendritic sink (LS) extended over 50-75 microns and was centered 100-150 microns ventral to the somatic layer. This proximal dendritic sink was of amplitude comparable with the SyS; it outlasted the latter and was not necessarily followed by a somatic PS. The LS was extinguished with the appearance of a PS, whereas the SyS persisted regardless of the presence of a PS. 4. After maximal stimuli the LS grew until it exceeded a threshold amplitude, and then, it started to move somatopetally as a continuously propagating sink (PrS). The average speed of propagation was approximately 0.2 m/s. In 0.5-0.7 ms the PrS reached the cell-body layer displacing the passive source that moved into the basal dendrites. The PrS then became the intensive sink corresponding to the main (negative) phase of the somatic PS. This was followed by the development of an active source in the soma layer, probably corresponding to the repolarization phase of the PS. 5. From these observations it appears that the LS and PrS are active dendritic responses. It may be inferred that, shortly after the synaptic currents enter the dendrites, depolarization of adjacent membranes causes the opening of low-threshold, voltage-dependent, slowly inactivating channels that generate the LS. If the depolarization resulting from the LS current is intense enough, another population of channels open that are also voltage-dependent but of higher threshold and faster inactivation.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
J. Makarova, J. M. Ibarz, S. Canals, and O. Herreras A Steady-State Model of Spreading Depression Predicts the Importance of an Unknown Conductance in Specific Dendritic Domains Biophys. J., June 15, 2007; 92(12): 4216 - 4232. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Canals, I. Makarova, L. Lopez-Aguado, C. Largo, J. M. Ibarz, and O. Herreras Longitudinal Depolarization Gradients Along the Somatodendritic Axis of CA1 Pyramidal Cells: A Novel Feature of Spreading Depression J Neurophysiol, August 1, 2005; 94(2): 943 - 951. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Canals, L. Lopez-Aguado, and O. Herreras Synaptically Recruited Apical Currents Are Required to Initiate Axonal and Apical Spikes in Hippocampal Pyramidal Cells: Modulation by Inhibition J Neurophysiol, February 1, 2005; 93(2): 909 - 918. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. R. Chen, G. Y. Shen, G. M. Shepherd, M. L. Hines, and J. Midtgaard Multiple Modes of Action Potential Initiation and Propagation in Mitral Cell Primary Dendrite J Neurophysiol, November 1, 2002; 88(5): 2755 - 2764. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Lopez-Aguado, J. M. Ibarz, P. Varona, and O. Herreras Structural Inhomogeneities Differentially Modulate Action Currents and Population Spikes Initiated in the Axon or Dendrites J Neurophysiol, November 1, 2002; 88(5): 2809 - 2820. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Kloosterman, P. Peloquin, and L. S. Leung Apical and Basal Orthodromic Population Spikes in Hippocampal CA1 In Vivo Show Different Origins and Patterns of Propagation J Neurophysiol, November 1, 2001; 86(5): 2435 - 2444. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Varona, J. M. Ibarz, L. Lopez-Aguado, and O. Herreras Macroscopic and Subcellular Factors Shaping Population Spikes J Neurophysiol, April 1, 2000; 83(4): 2192 - 2208. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Lopez-Aguado, J. M. Ibarz, and O. Herreras Modulation of Dendritic Action Currents Decreases the Reliability of Population Spikes J Neurophysiol, February 1, 2000; 83(2): 1108 - 1114. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kamondi, L. Acsady, and G. Buzsaki Dendritic Spikes Are Enhanced by Cooperative Network Activity in the Intact Hippocampus J. Neurosci., May 15, 1998; 18(10): 3919 - 3928. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. R. Chen, J. Midtgaard, and G. M. Shepherd Forward and Backward Propagation of Dendritic Impulses and Their Synaptic Control in Mitral Cells Science, October 17, 1997; 278(5337): 463 - 467. [Abstract] [Full Text] |
||||
![]() |
M. J. Dolleman-Van der Weel, F. H. Lopes da Silva, and M. P. Witter Nucleus Reuniens Thalami Modulates Activity in Hippocampal Field CA1 through Excitatory and Inhibitory Mechanisms J. Neurosci., July 15, 1997; 17(14): 5640 - 5650. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Largo, J. M. Ibarz, and O. Herreras Effects of the Gliotoxin Fluorocitrate on Spreading Depression and Glial Membrane Potential in Rat Brain In Situ J Neurophysiol, July 1, 1997; 78(1): 295 - 307. [Abstract] [Full Text] [PDF] |
||||
![]() |
N Spruston, Y Schiller, G Stuart, and B Sakmann Activity-dependent action potential invasion and calcium influx into hippocampal CA1 dendrites Science, April 14, 1995; 268(5208): 297 - 300. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |