 |
||||
|
||||
|
||||
|
||||
|
||||
The Journal of Neuroscience, November 29, 2006, 26(48):12447-12455; doi:10.1523/JNEUROSCI.2787-06.2006
Previous Article | Next Article
Neurobiology of Disease
Modular Propagation of Epileptiform Activity: Evidence for an Inhibitory Veto in Neocortex
Andrew J. Trevelyan,1,2 David Sussillo,1 Brendon O. Watson,1 andRafael Yuste1 1Howard Hughes Medical Institute, Department of Biological Sciences, Columbia University, New York, New York 10027, and 2School of Neurology, Neurobiology, and Psychiatry, The Medical School, University of Newcastle, Newcastle NE2 4HH, United Kingdom
Correspondence should be addressed to Andrew J. Trevelyan, School of Neurology, Neurobiology, and Psychiatry, The Medical School, University of Newcastle, Framlington Place, Newcastle NE2 4HH, UK. Email: andytrev{at}gmail.com
What regulates the spread of activity through cortical circuits? We present here data indicating a pivotal role for a vetoing inhibition restraining modules of pyramidal neurons. We combined fast calcium imaging of network activity with whole-cell recordings to examine epileptiform propagation in mouse neocortical slices. Epileptiform activity was induced by washing Mg2+ ions out of the slice. Pyramidal cells receive barrages of inhibitory inputs in advance of the epileptiform wave. The inhibitory barrages are effectively nullified at low doses of picrotoxin (2.5–5 µM). When present, however, these inhibitory barrages occlude an intense excitatory synaptic drive that would normally exceed action potential threshold by approximately a factor of 10. Despite this level of excitation, the inhibitory barrages suppress firing, thereby limiting further neuronal recruitment to the ictal event. Pyramidal neurons are recruited to the epileptiform event once the inhibitory restraint fails and are recruited in spatially clustered populations (150–250 µm diameter). The recruitment of the cells within a given module is virtually simultaneous, and thus epileptiform events progress in intermittent (0.5–1 Hz) steps across the cortical network. We propose that the interneurons that supply the vetoing inhibition define these modular circuit territories.
Key words: epilepsy; seizure; calcium imaging; inhibition; basket cell; pyramidal cell
Received June 30, 2006; revised Sept. 12, 2006; accepted Oct. 19, 2006.
Correspondence should be addressed to Andrew J. Trevelyan, School of Neurology, Neurobiology, and Psychiatry, The Medical School, University of Newcastle, Framlington Place, Newcastle NE2 4HH, UK. Email: andytrev{at}gmail.com
This article has been cited by other articles:
A. Bragin, A. Azizyan, J. Almajano, and J. Engel Jr
The Cause of the Imbalance in the Neuronal Network Leading to Seizure Activity Can Be Predicted by the Electrographic Pattern of the Seizure Onset
J. Neurosci., March 18, 2009; 29(11): 3660 - 3671.
[Abstract] [Full Text] [PDF]
M. Zhao, H. Ma, M. Suh, and T. H. Schwartz
Spatiotemporal Dynamics of Perfusion and Oximetry during Ictal Discharges in the Rat Neocortex
J. Neurosci., March 4, 2009; 29(9): 2814 - 2823.
[Abstract] [Full Text] [PDF]
A. J. Trevelyan, T. Baldeweg, W. van Drongelen, R. Yuste, and M. Whittington
The Source of Afterdischarge Activity in Neocortical Tonic Clonic Epilepsy
J. Neurosci., December 5, 2007; 27(49): 13513 - 13519.
[Abstract] [Full Text] [PDF]
A. J. Trevelyan, D. Sussillo, and R. Yuste
Feedforward Inhibition Contributes to the Control of Epileptiform Propagation Speed
J. Neurosci., March 28, 2007; 27(13): 3383 - 3387.
[Abstract] [Full Text] [PDF]
A. Devor, A. Trevelyan, and D. Kleinfeld
Is There a Common Origin to Surround-Inhibition as Seen Through Electrical Activity Versus Hemodynamic Changes? Focus on "Duration-Dependent Response in SI to Vibrotactile Stimulation in Squirrel Monkey"
J Neurophysiol, March 1, 2007; 97(3): 1880 - 1882.
[Full Text] [PDF]
|
|
|
|
 |
|