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Evidence for consolidation of neuronal assemblies after seizures in humans
MR. Bower, M. Stead, RS. Bower, MT. Kucewicz, V. Sulc, J. Cimbalnik, BH. Brinkmann, VM. Vasoli, EK. St Louis, FB. Meyer, WR. Marsh, GA. Worrell,
Language English Country United States
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1981 to 6 months ago
PubMed Central
from 1981 to 6 months ago
Europe PubMed Central
from 1981 to 6 months ago
Open Access Digital Library
from 1981-01-01
Open Access Digital Library
from 1981-01-01
- MeSH
- Action Potentials physiology MeSH
- Adult MeSH
- Electroencephalography MeSH
- Epilepsy, Temporal Lobe physiopathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Nerve Net physiopathology MeSH
- Neurons physiology MeSH
- Memory physiology MeSH
- Sleep physiology MeSH
- Seizures physiopathology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
The establishment of memories involves reactivation of waking neuronal activity patterns and strengthening of associated neural circuits during slow-wave sleep (SWS), a process known as "cellular consolidation" (Dudai and Morris, 2013). Reactivation of neural activity patterns during waking behaviors that occurs on a timescale of seconds to minutes is thought to constitute memory recall (O'Keefe and Nadel, 1978), whereas consolidation of memory traces may be revealed and served by correlated firing (reactivation) that appears during sleep under conditions suitable for synaptic modification (Buhry et al., 2011). Although reactivation has been observed in human neuronal recordings (Gelbard-Sagiv et al., 2008; Miller et al., 2013), reactivation during sleep has not, likely because data are difficult to obtain and the effect is subtle. Seizures, however, provide intense and synchronous, yet sparse activation (Bower et al., 2012) that could produce a stronger consolidation effect if seizures activate learning-related mechanisms similar to those activated by learned tasks. Continuous wide-bandwidth recordings from patients undergoing intracranial monitoring for drug-resistant epilepsy revealed reactivation of seizure-related neuronal activity during subsequent SWS, but not wakefulness. Those neuronal assemblies that were most strongly activated during seizures showed the largest correlation changes, suggesting that consolidation selectively strengthened neuronal circuits activated by seizures. These results suggest that seizures "hijack" physiological learning mechanisms and also suggest a novel epilepsy therapy targeting neuronal dynamics during post-seizure sleep.
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