Journal
EPILEPSIA
Volume 51, Issue 8, Pages 1587-1597Publisher
WILEY-BLACKWELL PUBLISHING, INC
DOI: 10.1111/j.1528-1167.2009.02420.x
Keywords
Ripple; Gap junction; Cellular automaton
Categories
Funding
- NIH/NINDS [R01NS044133]
- Alexander von Humboldt Stiftung
- IBM Corp.
- MRC Milstein Fund (United Kingdom)
- Wolfson Foundation
- Royal Society
- Newcastle upon Tyne Healthcare Charities Trust
- MRC [G0701048] Funding Source: UKRI
- Medical Research Council [G0701048] Funding Source: researchfish
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P>Purpose: We sought to characterize spatial and temporal patterns of electrocorticography (ECoG) very fast oscillations (> similar to 80 Hz, VFOs) prior to seizures in human frontotemporal neocortex, and to develop a testable network model of these patterns. Methods: ECoG data were recorded with subdural grids from two preoperative patients with seizures of frontal lobe onset in an epilepsy monitoring unit. VFOs were recorded from rat neocortical slices. A cellular automaton model of network oscillations was developed, extending ideas of Traub et al. (Neuroscience, 92, 1999, 407) and Lewis & Rinzel (Network: Comput Neural Syst, 11, 2000, 299); this model is based on postulated electrical coupling between pyramidal cell axons. Results: Layer 5 of rat neocortex, in vitro, can generate VFOs when chemical synapses are blocked. Human epileptic neocortex, in situ, produces preseizure VFOs characterized by the sudden appearance of blobs of activity that evolve into spreading wavefronts. When wavefronts meet, they coalesce and propagate perpendicularly but never pass through each other. This type of pattern has been described by Lewis & Rinzel in cellular automaton models with spatially localized connectivity, and is demonstrated here with 120,000- to 5,760,000-cell models. We provide a formula for estimating VFO period from structural parameters and estimate the spatial scale of the connectivity. Discussion: These data provide further evidence, albeit indirect, that preseizure VFOs are generated by networks of pyramidal neurons coupled by gap junctions, each predominantly confined to pairs of neurons having somata separated by < similar to 1-2 mm. Plausible antiepileptic targets are tissue mechanisms, such as pH regulation, that influence gap-junction conductance.
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