JN Miami Valley Hospital
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 82: 1965-1973, 1999;
0022-3077/99 $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 Tsau, Y.
Right arrow Articles by Wu, J.-Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsau, Y.
Right arrow Articles by Wu, J.-Y.

The Journal of Neurophysiology Vol. 82 No. 4 October 1999, pp. 1965-1973
Copyright ©1999 by the American Physiological Society

Epileptiform Activity Can Be Initiated in Various Neocortical Layers: An Optical Imaging Study

Yang Tsau, Li Guan, and Jian-Young Wu

Georgetown Institute for Cognitive and Computational Sciences, Georgetown University Medical Center, Washington, DC 20007

Tsau, Yang, Li Guan, and Jian-Young Wu. Epileptiform Activity Can Be Initiated in Various Neocortical Layers: An Optical Imaging Study. J. Neurophysiol. 82: 1965-1973, 1999. The initiation site for triggering epileptiform activity was investigated via optical imaging using voltage-sensitive dyes in the neocortical slice perfused with artificial cerebral spinal fluid containing nominally zero magnesium. The neocortical slices (400-µm thick) were harvested from Sprague-Dawley rats (P21-28). Optical imaging was made by using a high speed photodiode array. Spontaneous epileptiform activity emerged 20-40 min after the preparation was perfused with zero-magnesium solution. There was a good correspondence between electrical and optical signals (n = 46), although the details of the two recordings were somewhat different. The initiation sites were measured optically in 11 preparations. Among them, four were found to be located in superficial layers, two were found in middle layers, and five were found in deep layers. Repeated recordings revealed that these initiation sites were relatively stable; shifting of the initiation site was not observed. Therefore spontaneous epileptiform activity could be initiated in various cortical layers, from layer I to layer VI. The activation started from a small area <0.04 mm3 and spread smoothly from the initiation site to adjacent cortical areas, suggesting that the initiation site is very confined to one of the cortical layers. The initiation sites were distributed randomly in various cortical areas, and no higher probability was found in a special cortical region. Electrical stimulation delivered via a glass microelectrode filled with 2 M NaCl (2-5 MOmega ) could reliably trigger epileptiform activity that had the same characteristics as the spontaneous activity. The cortical neurons activated directly by the stimulation were around the electrode's tip and estimated to be within a 50-µm area, suggesting that only a few neurons were needed to form an initiation site. Because the timing for stimulation was arbitrary and the evoked events were initiated independent of discharges of neurons in any other layers, it is likely that the initiation site for epileptiform activity in various cortical layers is independent of the control of layer V pyramidal neurons. Together these finding suggest that the epileptiform focus is confined and can be formed in several (probably all) neocortical layers and in many cortical areas. The initiating neurons may be of different types because neuronal types in various cortical layers are different.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
S. Bolea, J. V. Sanchez-Andres, X. Huang, and J.-y. Wu
Initiation and Propagation of Neuronal Coactivation in the Developing Hippocampus
J Neurophysiol, January 1, 2006; 95(1): 552 - 561.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H.-t. Ma, C.-h. Wu, and J.-y. Wu
Initiation of Spontaneous Epileptiform Events in the Rat Neocortex In Vivo
J Neurophysiol, February 1, 2004; 91(2): 934 - 945.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
T. H. Schwartz
Optical Imaging of Epileptiform Events in Visual Cortex in Response to Patterned Photic Stimulation
Cereb Cortex, December 1, 2003; 13(12): 1287 - 1298.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J.-Y. Wu, L. Guan, L. Bai, and Q. Yang
Spatiotemporal Properties of an Evoked Population Activity in Rat Sensory Cortical Slices
J Neurophysiol, November 1, 2001; 86(5): 2461 - 2474.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
C. Wang, W. A. Wilson, and S. D. Moore
Role of NMDA, Non-NMDA, and GABA Receptors in Signal Propagation in the Amygdala Formation
J Neurophysiol, September 1, 2001; 86(3): 1422 - 1429.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
S. V. Szapiel
Optical Imaging and Its Role in Clinical Neurology
Arch Neurol, July 1, 2001; 58(7): 1061 - 1065.
[Full Text] [PDF]


Home page
J. Neurosci.Home page
M. A. Castro-Alamancos
Origin of Synchronized Oscillations Induced by Neocortical Disinhibition In Vivo
J. Neurosci., December 15, 2000; 20(24): 9195 - 9206.
[Abstract] [Full Text] [PDF]




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