JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 77: 621-631, 1997;
0022-3077/97 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pasquale, E. D.
Right arrow Articles by Noebels, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pasquale, E. D.
Right arrow Articles by Noebels, J. L.

The Journal of Neurophysiology Vol. 77 No. 2 February 1997, pp. 621-631
Copyright ©1997 The American Physiological Society

Increased Excitability and Inward Rectification in Layer V Cortical Pyramidal Neurons in the Epileptic Mutant Mouse Stargazer

Eric Di Pasquale, Karl D. Keegan, and Jeffrey L. Noebels

Developmental Neurogenetics Laboratory, Department of Neurology, Section of Neurophysiology, Baylor College of Medicine, Houston, Texas 77030

Di Pasquale, Eric, Karl D. Keegan, and Jeffrey L. Noebels. Increased excitability and inward rectification in layer V cortical pyramidal neurons in the epileptic mutant mouse stargazer. J. Neurophysiol. 77: 621-631, 1997. The excitability of layer V cortical pyramidal neurons was studied in vitro in the single-locus mutant mouse stargazer (stg), a genetic model of spike wave epilepsy. Field recordings in neocortical slices from mutant mice bathed in artificial cerebrospinal fluid revealed spontaneous synchronous network discharges that were never present in wild-type slices. Intracellular and whole cell recordings from stg/stg neurons in deep layers showed spontaneous giant depolarizing excitatory postsynaptic potentials generating bursts of action potentials, and a 78% reduction in the afterburst hyperpolarization. Whole cell recordings revealed gene-linked differences in active membrane properties in two types of regular spiking neurons. Single action potential rise and decay times were reduced, and the rheobase current was decreased by 68% in mutant cells. Plots of spike frequency-current relationships revealed that the gain of this relation was augmented by 29% in the mutant. Comparisons of visually identified pyramidal neuron firing properties in both genotypes revealed no difference in single action potential afterhyperpolarization. Voltage-clamp recordings showed an approximately threefold amplitude increase in a cesium-sensitive inward rectifier. No cell density or soma size differences were observed in the layer V pyramidal neuron population between the two genotypes. These results demonstrate an autonomous increase in cortical network excitability in a genetic epilepsy model. This defect could lower the threshold for aberrant thalamocortical spike wave oscillations in vivo, and may contribute to the mechanism of one form of inherited absence epilepsy.




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
H. L. Payne, W. M. Connelly, J. H. Ives, R. Lehner, B. Furtmuller, W. Sieghart, P. Tiwari, J. M. Lucocq, G. Lees, and C. L. Thompson
GABAA {alpha}6-Containing Receptors Are Selectively Compromised in Cerebellar Granule Cells of the Ataxic Mouse, Stargazer
J. Biol. Chem., October 5, 2007; 282(40): 29130 - 29143.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. H.P. Kole, A. U. Brauer, and G. J. Stuart
Inherited cortical HCN1 channel loss amplifies dendritic calcium electrogenesis and burst firing in a rat absence epilepsy model
J. Physiol., January 15, 2007; 578(2): 507 - 525.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. Kuisle, N. Wanaverbecq, A. L. Brewster, S. G. A. Frere, D. Pinault, T. Z. Baram, and A. Luthi
Functional stabilization of weakened thalamic pacemaker channel regulation in rat absence epilepsy
J. Physiol., August 15, 2006; 575(1): 83 - 100.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Sasaki, K. Huda, T. Inoue, M. Miyata, and K. Imoto
Impaired feedforward inhibition of the thalamocortical projection in epileptic Ca2+ channel mutant mice, tottering.
J. Neurosci., March 15, 2006; 26(11): 3056 - 3065.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Budde, L. Caputi, T. Kanyshkova, R. Staak, C. Abrahamczik, T. Munsch, and H.-C. Pape
Impaired Regulation of Thalamic Pacemaker Channels through an Imbalance of Subunit Expression in Absence Epilepsy
J. Neurosci., October 26, 2005; 25(43): 9871 - 9882.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
V. A. Letts, C. L. Mahaffey, B. Beyer, and W. N. Frankel
A targeted mutation in Cacng4 exacerbates spike-wave seizures in stargazer (Cacng2) mice
PNAS, February 8, 2005; 102(6): 2123 - 2128.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. H. Ives, S. Fung, P. Tiwari, H. L. Payne, and C. L. Thompson
Microtubule-associated Protein Light Chain 2 Is a Stargazin-AMPA Receptor Complex-interacting Protein in Vivo
J. Biol. Chem., July 23, 2004; 279(30): 31002 - 31009.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
I. Song, D. Kim, S. Choi, M. Sun, Y. Kim, and H.-S. Shin
Role of the {alpha}1G T-Type Calcium Channel in Spontaneous Absence Seizures in Mutant Mice
J. Neurosci., June 2, 2004; 24(22): 5249 - 5257.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
D. V. Vasilyev and M. E. Barish
Postnatal Development of the Hyperpolarization-Activated Excitatory Current Ih in Mouse Hippocampal Pyramidal Neurons
J. Neurosci., October 15, 2002; 22(20): 8992 - 9004.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
R. Felix
Channelopathies: ion channel defects linked to heritable clinical disorders
J. Med. Genet., October 1, 2000; 37(10): 729 - 740.
[Abstract] [Full Text]


Home page
J. Neurosci.Home page
K. Hashimoto, M. Fukaya, X. Qiao, K. Sakimura, M. Watanabe, and M. Kano
Impairment of AMPA Receptor Function in Cerebellar Granule Cells of Ataxic Mutant Mouse Stargazer
J. Neurosci., July 15, 1999; 19(14): 6027 - 6036.
[Abstract] [Full Text] [PDF]


Home page
Ann. N. Y. Acad. Sci.Home page
D. L. BURGESS and J. L. NOEBELS
Voltage-Dependent Calcium Channel Mutations in Neurological Disease
Ann. N.Y. Acad. Sci., April 30, 1999; 868(1): 199 - 212.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
S. G. Ryan
Ion Channels and the Genetic Contribution to Epilepsy
J Child Neurol, January 1, 1999; 14(1): 58 - 66.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
M. Steriade, F. Amzica, D. Neckelmann, and I. Timofeev
Spike-Wave Complexes and Fast Components of Cortically Generated Seizures. II. Extra- and Intracellular Patterns
J Neurophysiol, September 1, 1998; 80(3): 1456 - 1479.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online