|
|
||||||||
The Journal of Neurophysiology Vol. 82 No. 5 November 1999, pp. 2130-2142
Copyright ©1999 by the American Physiological Society
Department of Physiology and Biophysics, St. Mary's Hospital Medical School, Imperial College, London W2 1PG; and Department of Neurophysiology, Division of Neuroscience, The Medical School, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom
Borck, Cornelius and
John G. R. Jefferys.
Seizure-Like Events in Disinhibited Ventral Slices of Adult
Rat Hippocampus. J. Neurophysiol. 82: 2130-2142, 1999. Epileptic discharges lasting 2-90 s, were
studied in vitro in slices from the ventral hippocampus of adult rats,
in which inhibition was blocked acutely with bicuculline methiodide
(BMI, 5-30 µM) and potassium ([K+]o)
raised to 5 mM. These seizure-like events (SLEs) comprised three
distinct phases, called here primary,
secondary, and tertiary bursts. Primary
bursts lasted 90-150 ms. Secondary bursts lasted a further 70-250 ms,
comprising a short series of afterdischarges riding on the same
depolarization as the primary burst. Finally a train of tertiary bursts
started with a peak frequency of 5-10 Hz and could last >1 min.
Slices from the ventral hippocampus showed significantly higher
susceptibility to SLEs than did dorsal slices. SLEs proved sensitive to
-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor
antagonists. They were insensitive to
N-methyl-D-aspartate (NMDA) receptor
antagonists; 50 µl D-2-amino-5-phosphonopentanoic acid
(D-AP5) did block the transient secondary bursts
selectively. SLEs were restricted to the hippocampus proper even if the
entorhinal cortex was present. Entorhinal bursts could last <2 s and
were only coupled with hippocampal bursts in a minority of slices. Reentry of epileptic bursts occasionally occurred during interictal discharges, but not during the later stages of SLEs. Full-length SLEs
always started in CA3 region and could be recorded in minislices containing CA3 plus dentate hilus. Ion-sensitive microelectrodes revealed that interictal discharges were followed by short (2-3 s)
[K+]o waves, peaking at ~7.5 mM. SLEs were
always accompanied by increases in [K+]o
reaching ~8.5 mM at the start of tertiary bursts;
[K+]o then increased more slowly to a ceiling
of 11-12 mM. After the end of each SLE,
[K+]o fell back to baseline within 10-15 s.
SLEs were accompanied by significant increase in synaptic activity,
compared with baseline and/or interictal activity, estimated by the
variance of the intracellular signal in the absence of epileptic bursts
and action potentials (0.38 mV2, compared with 0.13 mV2, and 0.1 mV2, respectively). No significant
increases were observed in the interval preceding spontaneous
interictal activity. These studies show that focal assemblies of
hippocampal neurons, without long reentrant loops, are sufficient for
the generation of SLEs. We propose that a key factor in the transition
from interictal activity to SLEs is an increase in axonal and terminal
excitability, resulting, at least in part, from elevations in
[K+]o.
This article has been cited by other articles:
![]() |
Y. Fujiwara-Tsukamoto, Y. Isomura, and M. Takada Comparable GABAergic Mechanisms of Hippocampal Seizurelike Activity in Posttetanic and Low-Mg2+ Conditions J Neurophysiol, March 1, 2006; 95(3): 2013 - 2019. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Wu, M. N. Asl, J. Gillis, F. K. Skinner, and L. Zhang An In Vitro Model of Hippocampal Sharp Waves: Regional Initiation and Intracellular Correlates J Neurophysiol, July 1, 2005; 94(1): 741 - 753. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Wu, W. P. Luk, J. Gillis, F. Skinner, and L. Zhang Size Does Matter: Generation of Intrinsic Network Rhythms in Thick Mouse Hippocampal Slices J Neurophysiol, April 1, 2005; 93(4): 2302 - 2317. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. I. Netoff, R. Clewley, S. Arno, T. Keck, and J. A. White Epilepsy in Small-World Networks J. Neurosci., September 15, 2004; 24(37): 8075 - 8083. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Fujiwara-Tsukamoto, Y. Isomura, K. Kaneda, and M. Takada Synaptic interactions between pyramidal cells and interneurone subtypes during seizure-like activity in the rat hippocampus J. Physiol., June 15, 2004; 557(3): 961 - 979. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. T. Finnerty and J.G.R. Jefferys Investigation of the Neuronal Aggregate Generating Seizures in the Rat Tetanus Toxin Model of Epilepsy J Neurophysiol, December 1, 2002; 88(6): 2919 - 2927. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. J. Gluckman, H. Nguyen, S. L. Weinstein, and S. J. Schiff Adaptive Electric Field Control of Epileptic Seizures J. Neurosci., January 15, 2001; 21(2): 590 - 600. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Kohling, M. Vreugdenhil, E. Bracci, and J. G. R. Jefferys Ictal Epileptiform Activity Is Facilitated by Hippocampal GABAA Receptor-Mediated Oscillations J. Neurosci., September 15, 2000; 20(18): 6820 - 6829. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Kager, W. J. Wadman, and G. G. Somjen Simulated Seizures and Spreading Depression in a Neuron Model Incorporating Interstitial Space and Ion Concentrations J Neurophysiol, July 1, 2000; 84(1): 495 - 512. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. T. Finnerty and J.G.R. Jefferys 9-16 Hz Oscillation Precedes Secondary Generalization of Seizures in the Rat Tetanus Toxin Model of Epilepsy J Neurophysiol, April 1, 2000; 83(4): 2217 - 2226. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |