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Hippocampal Sharp Wave Bursts Coincide with Neocortical "up-state" Transitions

Overview
Journal Learn Mem
Specialty Neurology
Date 2004 Dec 4
PMID 15576887
Citations 139
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Abstract

The sleeping neocortex shows nested oscillatory activity in different frequency ranges, characterized by fluctuations between "up-states" and "down-states." High-density neuronal ensemble recordings in rats now reveal the interaction between synchronized activity in the hippocampus and neocortex: Electroencephalographic sharp waves in the hippocampus were more probable during down-states than during up-states, and tended to coincide with transitions from down-states to up-states. The form of cortical activity fluctuations and their interactions with sharp waves depend on sleep depth: In deeper sleep stages, characterized by strong neocortical oscillation in the delta range or slower (approximately 0.8-4 Hz), sharp-wave-triggered peri-event time histograms (PETH) are consistent with a longer duration for down-states than for up-states. In lighter sleep, the sharp-wave-triggered PETH suggested longer up-states than down-states. These results highlight the interplay in the hippocampal/neocortical loop: Decreased neocortical input during down-states may be a factor in generation of sharp waves. In turn, sharp waves may facilitate down-to-up transitions. This interplay may reflect joint memory trace reactivation in the hippocampus and in the neocortex, possibly contributing to consolidation of long-term memory: Off-line reactivation of recent neural activity patterns in the hippocampus occurs during 50-100-msec electroencephalographic sharp waves, corresponding to pyramidal-cell population bursts. The neocortical up-states starting in correspondence with sharp waves may be influenced by the reactivated information carried by the hippocampal sharp wave.

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References
1.
Louie K, Wilson M . Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep. Neuron. 2001; 29(1):145-56. DOI: 10.1016/s0896-6273(01)00186-6. View

2.
Plihal W, Born J . Effects of early and late nocturnal sleep on priming and spatial memory. Psychophysiology. 1999; 36(5):571-82. View

3.
Maquet P . The role of sleep in learning and memory. Science. 2001; 294(5544):1048-52. DOI: 10.1126/science.1062856. View

4.
Hoffman K, McNaughton B . Coordinated reactivation of distributed memory traces in primate neocortex. Science. 2002; 297(5589):2070-3. DOI: 10.1126/science.1073538. View

5.
Sirota A, Csicsvari J, Buhl D, Buzsaki G . Communication between neocortex and hippocampus during sleep in rodents. Proc Natl Acad Sci U S A. 2003; 100(4):2065-9. PMC: 149959. DOI: 10.1073/pnas.0437938100. View