The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Local sleep in awake rats
Open accessAbstract
In an awake state, neurons in the cerebral cortex fire irregularly and electroencephalogram (EEG) recordings display low-amplitude, high-frequency fluctuations. During sleep, neurons oscillate between 'on' periods, when they fire as in an awake brain, and 'off' periods, when they stop firing altogether and the EEG displays high-amplitude slow waves. However, what happens to neuronal firing after a long period of being awake is not known. Here we show that in freely behaving rats after a long period in an awake state, cortical neurons can go briefly 'offline' as in sleep, accompanied by slow waves in the local EEG. Neurons often go offline in one cortical area but not in another, and during these periods of 'local sleep', the incidence of which increases with the duration of the awake state, rats are active and display an 'awake' EEG. However, they are progressively impaired in a sugar pellet reaching task. Thus, although both the EEG and behaviour indicate wakefulness, local populations of neurons in the cortex may be falling asleep, with negative consequences for performance.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, as distinct qualitative differences between both frequency bands have not been confirmed, the decrease in SWA across sleep appears to be most parsimoniously explained by a decrease in the incidence of high-amplitude slow waves (1267).”
From About Sleep's Role in Memory (2013) · cites this paper as [1267]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“in demonstrating that the encoding of information during waking enhances subsequent SWA in specific brain regions, these studies provide compelling evidence that SWA is regulated locally in addition to its global regulation by brain stem and diencephalic structures (672, 859, 975, 1267).”
From About Sleep's Role in Memory (2013) · cites this paper as [1267]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“these studies provide compelling evidence that SWA is regulated locally in addition to its global regulation by brain stem and diencephalic structures (672, 859, 975, 1267).”
From About Sleep's Role in Memory (2013) · cites this paper as [1267]
Experimental — accuracy not yet measuredIn the citing paper
“Likewise, the intensity of slow waves in the cortical field potential slowly increases over the active period, in direct relationship to more frequent and longer sleep bouts”
From Waking state: rapid variations modulate neural and behavioral responses (2015) · cites this paper as Vyazovskiy et al., 2011
In the citing paper
“In addition to the phenomena described above, the degree of habituation to an experimental situation may also change the prevalence of low frequency rhythms in the cortex”
From Waking state: rapid variations modulate neural and behavioral responses (2015) · cites this paper as Vyazovskiy et al., 2011
In the citing paper
“In one recent study, the ability of animals to perform a difficult pellet retrieval task was significantly impaired during the appearance of Off periods in cortical networks, supporting the hypothesis that these sudden, but brief, cessations of cortical activity are detrimental to behaviorally relevant cortical operation (Vyazovskiy et al., 2011)”
From Waking state: rapid variations modulate neural and behavioral responses (2015) · cites this paper as Vyazovskiy et al., 2011
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
An Energy Budget for Signaling in the Grey Matter of the Brain
Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543
Van Dongen, H. P. A., Maislin, G., Mullington, J. M., & Dinges, D. F. (2003) · Sleep · doi:10.1093/sleep/26.2.117 · Cited by 3,173
Sleep function and synaptic homeostasis
Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151
Self-citationHuber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854
Self-citationSleep Homeostasis and Models of Sleep Regulation
Borb, A. A., & Achermann, P. (1999) · Journal of Biological Rhythms · doi:10.1177/074873099129000894 · Cited by 1,546
Effects of sleep deprivation on cognition
Killgore, W. D. S. (2010) · Progress in Brain Research · doi:10.1016/b978-0-444-53702-7.00007-5 · Cited by 1,421
Natural waking and sleep states: a view from inside neocortical neurons
Steriade, M., Timofeev, I., & Grenier, F. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.5.1969 · Cited by 1,296
Learning-Induced LTP in Neocortex
Rioult-Pedotti, M.-S., Friedman, D. J., & Donoghue, J. P. (2000) · Science · doi:10.1126/science.290.5491.533 · Cited by 1,014
Regional Slow Waves and Spindles in Human Sleep
Nir, Y., Staba, R. J., Andrillon, T., Vyazovskiy, V. V., Cirelli, C., Fried, I., & Tononi, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.043 · Cited by 924
Self-citation
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
Tononi, G., & Cirelli, C. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.025 · Cited by 2,356
Self-citationControl of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
An opportunity cost model of subjective effort and task performance
Kurzban, R., Duckworth, A., Kable, J. W., & Myers, J. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12003196 · Cited by 1,381
The sleep-deprived human brain
Krause, A. J., Simon, E. B., Mander, B. A., Greer, S. M., Saletin, J. M., Goldstein-Piekarski, A. N., & Walker, M. P. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.55 · Cited by 1,200
Neural Circuitry of Wakefulness and Sleep
Scammell, T. E., Arrigoni, E., & Lipton, J. O. (2017) · Neuron · doi:10.1016/j.neuron.2017.01.014 · Cited by 966
Regional Slow Waves and Spindles in Human Sleep
Nir, Y., Staba, R. J., Andrillon, T., Vyazovskiy, V. V., Cirelli, C., Fried, I., & Tononi, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.043 · Cited by 924
Self-citationSleep, insomnia, and depression
Riemann, D. W., Krone, L. B., Wulff, K., & Nissen, C. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0411-y · Cited by 901
Waking state: rapid variations modulate neural and behavioral responses
McGinley, M. J., Vinck, M., Reimer, J., Batista-Brito, R., Zagha, E., Cadwell, C. R., Tolias, A. S., Cardin, J. A., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.012 · Cited by 801
“Likewise, the intensity of slow waves in the cortical field potential slowly increases over the active period, in direct relationship to more frequent and longer sleep bouts (Curie et al., 2013; Hasan et al., 2012; Vyazovskiy et al., 2011).”
InfluentialCortical membrane potential signature of optimal states for sensory signal detection
McGinley, M. J., David, S. V., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.038 · Cited by 728
Ultrastructural evidence for synaptic scaling across the wake/sleep cycle
de Vivo, L., Bellesi, M., Marshall, W., Bushong, E. A., Ellisman, M. H., Tononi, G., & Cirelli, C. (2017) · Science · doi:10.1126/science.aah5982 · Cited by 574
Self-citationRoh, J. H., Huang, Y., Bero, A. W., Kasten, T., Stewart, F. R., Bateman, R. J., & Holtzman, D. M. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004291 · Cited by 563
Brain mechanisms of insomnia: new perspectives on causes and consequences
Someren, E. J. W. V. (2020) · Physiological Reviews · doi:10.1152/physrev.00046.2019 · Cited by 578
An electrophysiological marker of arousal level in humans
Lendner, J. D., Helfrich, R. F., Mander, B. A., Romundstad, L. G., Lin, J. J., Walker, M. P., Larsson, P. G., & Knight, R. T. (2020) · eLife · doi:10.7554/elife.55092 · Cited by 425
Sleep deprivation, vigilant attention, and brain function: a review
Hudson, A. N., Dongen, H. P. A. V., & Honn, K. A. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0432-6 · Cited by 426
Rapid fragmentation of neuronal networks at the onset of propofol-induced unconsciousness
Lewis, L. D., Weiner, V. S., Mukamel, E. A., Donoghue, J., Eskandar, E. N., Madsen, J. R., Anderson, W. S., Hochberg, L. R., Cash, S. S., Brown, E. N., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210907109 · Cited by 387
Astrocytes regulate cortical state switching in vivo
Poskanzer, K. E., & Yuste, R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520759113 · Cited by 377
Sleep and the single neuron: the role of global slow oscillations in individual cell rest
Vyazovskiy, V. V., & Harris, K. D. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3494 · Cited by 386
Self-citationFunctions and Mechanisms of Sleep
Zielinski, M. R., McKenna, J. T., & McCarley, R. W. (2016) · AIMS neuroscience · doi:10.3934/neuroscience.2016.1.67 · Cited by 392
Evidence that birds sleep in mid-flight
Rattenborg, N. C., Voirin, B., Cruz, S. M., Tisdale, R. K., Dell’Omo, G., Lipp, H., Wikelski, M. C., & Vyssotski, A. L. (2016) · Nature Communications · doi:10.1038/ncomms12468 · Cited by 341
Forward-genetics analysis of sleep in randomly mutagenized mice
Funato, H., Miyoshi, C., Fujiyama, T., Kanda, T., Sato, M., Wang, Z., Ma, J., Nakane, S., Tomita, J., Ikkyu, A., et al. (2016) · Nature · doi:10.1038/nature20142 · Cited by 335
Sleep and waking modulate spine turnover in the adolescent mouse cortex
Maret, S., Faraguna, U., Nelson, A. B., Cirelli, C., & Tononi, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2934 · Cited by 315
Self-citationSleep Neurophysiological Dynamics Through the Lens of Multitaper Spectral Analysis
Prerau, M. J., Brown, R. E., Bianchi, M. T., Ellenbogen, J. M., & Purdon, P. L. (2016) · Physiology · doi:10.1152/physiol.00062.2015 · Cited by 324
Neuromodulation of brain state and behavior
McCormick, D. A., Nestvogel, D. B., & He, B. J. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-100219-105424 · Cited by 303
Schmidt, M. H. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.08.001 · Cited by 291
The Slow Oscillation in Cortical and Thalamic Networks: Mechanisms and Functions
Neske, G. T. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00088 · Cited by 296
Neuronal Mechanisms for Sleep/Wake Regulation and Modulatory Drive
Eban-Rothschild, A., Appelbaum, L., & de Lecea, L. (2018) · Neuropsychopharmacology · doi:10.1038/npp.2017.294 · Cited by 282
Oscillating circuitries in the sleeping brain
Adamantidis, A. R., Gutierrez Herrera, C., & Gent, T. C. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0223-4 · Cited by 281
Slow-wave sleep: From the cell to the clinic
Léger, D., Debellemanière, E., Rabat, A., Bayon, V., Benchenane, K., & Chennaoui, M. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2018.01.008 · Cited by 284
Adaptive Sleep Loss in Polygynous Pectoral Sandpipers
Lesku, J. A., Rattenborg, N. C., Vâlcu, M., Vyssotski, A. L., Kuhn, S., Kümmeth, F., Heidrich, W., & Kempenaers, B. (2012) · Science · doi:10.1126/science.1220939 · Cited by 260
Genzel, L., Kroes, M. C. W., Dresler, M., & Battaglia, F. P. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.10.002 · Cited by 285
Making Waves: Initiation and Propagation of Corticothalamic Ca2+ Waves In Vivo
Stroh, A., Adelsberger, H., Groh, A., Rühlmann, C., Fischer, S., Schierloh, A., Deisseroth, K. A., & Konnerth, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.031 · Cited by 249
Humans can learn new information during sleep
Arzi, A., Shedlesky, L., Ben-Shaul, M., Nasser, K., Oksenberg, A., Hairston, I. S., & Sobel, N. (2012) · Nature Neuroscience · doi:10.1038/nn.3193 · Cited by 253
Enhancement of sleep slow waves: underlying mechanisms and practical consequences
Bellesi, M., Riedner, B. A., Garcia-Molina, G. N., Cirelli, C., & Tononi, G. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00208 · Cited by 239
Self-citationImaging neural circuit dynamics with a voltage-sensitive fluorescent protein
Akemann, W., Mutoh, H., Perron, A., Park, Y. K., Iwamoto, Y., & Knöpfel, T. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00452.2012 · Cited by 237
Unraveling the evolutionary determinants of sleep
Joiner, W. J. (2016) · Current Biology · doi:10.1016/j.cub.2016.08.068 · Cited by 232
Potential role of orexin and sleep modulation in the pathogenesis of Alzheimer’s disease
Roh, J. H., Jiang, H., Finn, M. B., Stewart, F. R., Mahan, T. E., Cirrito, J. R., Heda, A., Snider, B. J., Li, M., Yanagisawa, M., et al. (2014) · Journal of Experimental Medicine · doi:10.1084/jem.20141788 · Cited by 237
The Input-Output Relationship of the Cholinergic Basal Forebrain
Gielow, M. R., & Záborszky, L. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.060 · Cited by 243
The claustrum coordinates cortical slow-wave activity
Narikiyo, K., Mizuguchi, R., Ajima, A., Mitsui, S., Shiozaki, M., Hamanaka, H., Johansen, J. P., Mori, K., & Yoshihara, Y. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0625-7 · Cited by 237
Properties of Slow Oscillation during Slow-Wave Sleep and Anesthesia in Cats
Chauvette, S., Crochet, S., Volgushev, M., & Timofeev, I. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2339-11.2011 · Cited by 238
Circadian regulation of human cortical excitability
Ly, J. Q. M., Gaggioni, G., Chellappa, S. L., Papachilleos, S., Brzozowski, A., Borsu, C., Rosanova, M., Sarasso, S., Middleton, B., Luxen, A., et al. (2016) · Nature Communications · doi:10.1038/ncomms11828 · Cited by 226
Local Experience-Dependent Changes in the Wake EEG after Prolonged Wakefulness
Hung, C., Sarasso, S., Ferrarelli, F., Riedner, B. A., Ghilardi, M. F., Cirelli, C., & Tononi, G. (2012) · SLEEP · doi:10.5665/sleep.2302 · Cited by 233
Self-citationEssential Thalamic Contribution to Slow Waves of Natural Sleep
David, F., Schmiedt, J. T., Taylor, H. L., Orbán, G., Giovanni, G. D., Uebele, V. N., Renger, J. J., Lambert, R. C., Leresche, N., & Crunelli, V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3169-13.2013 · Cited by 234
Predicting lapses of attention with sleep-like slow waves
Andrillon, T., Burns, A. C., Mackay, T., Windt, J., & Tsuchiya, N. (2021) · Nature Communications · doi:10.1038/s41467-021-23890-7 · Cited by 236
Napping: a public health issue. From epidemiological to laboratory studies
Faraut, B., Andrillon, T., Vecchierini, M.-F., & Leger, D. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.09.002 · Cited by 217
Local aspects of sleep and wakefulness
Siclari, F., & Tononi, G. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.05.008 · Cited by 220
Self-citationThalamic reticular nucleus induces fast and local modulation of arousal state
Lewis, L. D., Voigts, J., Flores, F. J., Schmitt, L. I., Wilson, M. A., Halassa, M. M., & Brown, E. N. (2015) · eLife · doi:10.7554/elife.08760 · Cited by 215
Specific basal forebrain-cortical cholinergic circuits coordinate cognitive operations
Záborszky, L., Gombkoto, P., Varsanyi, P., Gielow, M. R., Poe, G., Role, L. W., Ananth, M., Rajebhosale, P., Talmage, D. A., Hasselmo, M. E., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1676-18.2018 · Cited by 202
Hinard, V., Mikhail, C., Pradervand, S., Curie, T., Houtkooper, R. H., Auwerx, J. H., Franken, P., & Tafti, M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2306-12.2012 · Cited by 209
Consciousness among delta waves: a paradox?
Frohlich, J., Toker, D., & Monti, M. M. (2021) · Brain · doi:10.1093/brain/awab095 · Cited by 204
Selective neuronal lapses precede human cognitive lapses following sleep deprivation
Nir, Y., Andrillon, T., Marmelshtein, A., Suthana, N., Cirelli, C., Tononi, G., & Fried, I. (2017) · Nature Medicine · doi:10.1038/nm.4433 · Cited by 196
Self-citationBrain state dependent activity in the cortex and thalamus
McCormick, D. A., McGinley, M. J., & Salkoff, D. B. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.10.003 · Cited by 198
A global brain state underlies C. elegans sleep behavior
Nichols, A. L. A., Eichler, T., Latham, R., & Zimmer, M. (2017) · Science · doi:10.1126/science.aam6851 · Cited by 195
The consequences of sleep deprivation on cognitive performance
Khan, M., & Al-Jahdali, H. H. (2023) · Neurosciences · doi:10.17712/nsj.2023.2.20220108 · Cited by 218
Lag structure in resting-state fMRI
Mitra, A., Snyder, A. Z., Hacker, C. D., & Raichle, M. E. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00804.2013 · Cited by 188
Zagha, E., & McCormick, D. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.010 · Cited by 191
Breathing coordinates cortico-hippocampal dynamics in mice during offline states
Karalis, N., & Sirota, A. (2022) · Nature Communications · doi:10.1038/s41467-022-28090-5 · Cited by 179
Local Slow Waves in Superficial Layers of Primary Cortical Areas during REM Sleep
Funk, C. M., Honjoh, S., Rodriguez, A. V., Cirelli, C., & Tononi, G. (2016) · Current Biology · doi:10.1016/j.cub.2015.11.062 · Cited by 178
Self-citationThe Impact of Cortical Deafferentation on the Neocortical Slow Oscillation
Lemieux, M., Chen, J., Lonjers, P., Bazhenov, M., & Timofeev, I. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1156-13.2014 · Cited by 182
NREM and REM Sleep: Complementary Roles in Recovery after Wakefulness
Vyazovskiy, V. V., & Delogu, A. (2014) · The Neuroscientist · doi:10.1177/1073858413518152 · Cited by 169
Self-citationThalamocortical synchronization during induction and emergence from propofol-induced unconsciousness
Flores, F. J., Hartnack, K. E., Fath, A. B., Kim, S., Wilson, M. A., Brown, E. N., & Purdon, P. L. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1700148114 · Cited by 176
Sleep-wake control and the thalamus
Gent, T. C., Bassetti, C. L., & Adamantidis, A. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.08.002 · Cited by 175
The thalamocortical network as a single slow wave-generating unit
Crunelli, V., David, F., Lörincz, M. L., & Hughes, S. W. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.001 · Cited by 171
Schmitt, L. I., Sims, R. E., Dale, N., & Haydon, P. G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5689-11.2012 · Cited by 162
Deconstructing and reconstructing cognitive performance in sleep deprivation
Jackson, M. L., Glenn Gunzelmann, A., Whitney, P. J., Hinson, J. M., Belenky, G. L., Rabat, A., & Dongen, H. P. A. V. (2012) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2012.06.007 · Cited by 169
UP-DOWN cortical dynamics reflect state transitions in a bistable network
Jercog, D., Roxin, A., Barthó, P., Luczak, A., Compte, A., & de la Rocha, J. (2017) · eLife · doi:10.7554/elife.22425 · Cited by 166
Gating of Sensory Input by Spontaneous Cortical Activity
Luczak, A., Barthó, P., & Harris, K. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2928-12.2013 · Cited by 161
Regional Delta Waves In Human Rapid Eye Movement Sleep
Bernardi, G., Betta, M., Ricciardi, E., Pietrini, P., Tononi, G., & Siclari, F. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.2298-18.2019 · Cited by 156
Self-citationTapping the Brakes: Cellular and Synaptic Mechanisms that Regulate Thalamic Oscillations
Fogerson, P. M., & Huguenard, J. R. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.024 · Cited by 155
Bernardi, G., Siclari, F., Yu, X., Zennig, C., Bellesi, M., Ricciardi, E., Cirelli, C., Ghilardi, M. F., Pietrini, P., & Tononi, G. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4567-14.2015 · Cited by 153
Self-citationSleep recalibrates homeostatic and associative synaptic plasticity in the human cortex
Kuhn, M., Wolf, E., Maier, J. G., Mainberger, F., Feige, B., Schmid, H., Bürklin, J., Maywald, S., Mall, V., Jung, N. H., et al. (2016) · Nature Communications · doi:10.1038/ncomms12455 · Cited by 152
A role for the cortex in sleep–wake regulation
Krone, L. B., Yamagata, T., Blanco‐Duque, C., Guillaumin, M. C. C., Kahn, M. C., van der Vinne, V., McKillop, L. E., Tam, S. K. E., Peirson, S. N., Akerman, C. J., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00894-6 · Cited by 159
Self-citationA neuron–glia lipid metabolic cycle couples daily sleep to mitochondrial homeostasis
Haynes, P. R., Pyfrom, E. S., Li, Y., Stein, C., Cuddapah, V. A., Jacobs, J. A., Yue, Z., & Sehgal, A. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01568-1 · Cited by 149
Schmidt, M., Bakker, R., Shen, K., Bezgin, G., Diesmann, M., & van Albada, S. J. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006359 · Cited by 157
Amyloid-β diurnal pattern: possible role of sleep in Alzheimer's disease pathogenesis
Lucey, B. P., & Bateman, R. J. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.03.035 · Cited by 156
Central control of cardiovascular function during sleep
Silvani, A., & Dampney, R. A. L. (2013) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00554.2013 · Cited by 143
Krueger, J. M., Nguyen, J., Dykstra-Aiello, C., & Taishi, P. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2018.10.001 · Cited by 142
Resting state EEG correlates of memory consolidation
Brokaw, K., Tishler, W., Manceor, S., Hamilton, K., Gaulden, A. D., Parr, E., & Wamsley, E. J. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.01.008 · Cited by 149
Top-down cortical input during NREM sleep consolidates perceptual memory
Miyamoto, D., Hirai, D., Fung, C. C. A., Inutsuka, A., Odagawa, M., Suzuki, T., Boehringer, R., Adaikkan, C., Matsubara, C., Matsuki, N., et al. (2016) · Science · doi:10.1126/science.aaf0902 · Cited by 135
Meisel, C., Schulze‐Bonhage, A., Freestone, D. R., Cook, M. J., Achermann, P., & Plenz, D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513716112 · Cited by 138
Riemann, D. W., Dressle, R. J., Benz, F., Spiegelhalder, K., Johann, A. F., Nissen, C., Hertenstein, E., Baglioni, C., Palagini, L., Krone, L. B., et al. (2024) · Journal of Sleep Research · doi:10.1111/jsr.14252 · Cited by 138
The vigilant sleeper: neural mechanisms of sensory (de)coupling during sleep
Andrillon, T., & Kouider, S. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.12.002 · Cited by 133
Nir, Y., Vyazovskiy, V. V., Cirelli, C., Banks, M. I., & Tononi, G. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht328 · Cited by 132
Self-citationReal-time dialogue between experimenters and dreamers during REM sleep
Konkoly, K. R., Appel, K., Chabani, E., Mangiaruga, A., Gott, J., Mallett, R., Caughran, B., Witkowski, S., Whitmore, N. W., Mazurek, C. Y., et al. (2021) · Current Biology · doi:10.1016/j.cub.2021.01.026 · Cited by 131
Identification of Neurons with a Privileged Role in Sleep Homeostasis in Drosophila melanogaster
Seidner, G. A., Robinson, J. E., Wu, M., Worden, K., Masek, P., Roberts, S. W., Keene, A. C., & Joiner, W. J. (2015) · Current Biology · doi:10.1016/j.cub.2015.10.006 · Cited by 134
Brain energetics during the sleep-wake cycle
DiNuzzo, M., & Nedergaard, M. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.09.010 · Cited by 130
The interconnected causes and consequences of sleep in the brain
Lewis, L. D. (2021) · Science · doi:10.1126/science.abi8375 · Cited by 133
Cleaning the sleeping brain – the potential restorative function of the glymphatic system
Hauglund, N. L., Pavan, C., & Nedergaard, M. (2020) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.10.020 · Cited by 129
Local sleep-like cortical reactivity in the awake brain after focal injury
Sarasso, S., D’Ambrosio, S., Fecchio, M., Casarotto, S., Viganò, A., Landi, C., Mattavelli, G., Gosseries, O., Quarenghi, M., Laureys, S., et al. (2020) · Brain · doi:10.1093/brain/awaa338 · Cited by 128
Ongoing physiological processes in the cerebral cortex
Leopold, D. A., & Maier, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.059 · Cited by 127
Neurovascular coupling and bilateral connectivity during nrem and rem sleep
Turner, K. L., Gheres, K. W., Proctor, E. A., & Drew, P. J. (2020) · eLife · doi:10.7554/elife.62071 · Cited by 130
Andrillon, T., Windt, J., Silk, T. J., Drummond, S. P. A., Bellgrove, M. A., & Tsuchiya, N. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00949 · Cited by 133
Sleep-related epileptic behaviors and non-REM-related parasomnias: Insights from stereo-EEG
Gibbs, S. A., Proserpio, P., Terzaghi, M., Pigorini, A., Sarasso, S., Russo, G. L., Tassi, L., & Nobili, L. (2015) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.05.002 · Cited by 124
The Cortical States of Wakefulness
Poulet, J. F. A., & Crochet, S. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00064 · Cited by 126
Spontaneous behaviors drive multidimensional, brain-wide activityPreprint
Stringer, C., Pachitariu, M., Steinmetz, N. A., Reddy, C. B., Carandini, M., & Harris, K. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/306019 · Cited by 123
Sleep slow oscillation and plasticity
Timofeev, I., & Chauvette, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.019 · Cited by 121
Gaskell, A. L., Hight, D., Winders, J., Tran, G., Defresne, A., Bonhomme, V. L., Raz, A., SLEIGH, J. W., & Sanders, R. D. (2017) · British Journal of Anaesthesia · doi:10.1093/bja/aex170 · Cited by 123
How networks communicate: propagation patterns in spontaneous brain activity
Mitra, A., & Raichle, M. E. (2016) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0546 · Cited by 118
Tanabe, S., Mohanty, R., Lindroth, H. L., Casey, C., Ballweg, T., Farahbakhsh, Z. Z., Krause, B. M., Prabhakaran, V., Banks, M. I., & Sanders, R. D. (2020) · British Journal of Anaesthesia · doi:10.1016/j.bja.2020.02.027 · Cited by 115
Time to Be SHY? Some Comments on Sleep and Synaptic Homeostasis
Tononi, G., & Cirelli, C. (2012) · Neural Plasticity · doi:10.1155/2012/415250 · Cited by 124
Self-citation
Metadata
- Authors
- Vyazovskiy, V. V., Olcese, U., Hanlon, E. C., Nir, Y., Cirelli, C., & Tononi, G.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Tononi, Giulio
- Venue
- Nature
- Published
- 2011-04
- Volume
- 472
- Issue
- 7344
- Pages
- 443-447
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3085007
- OpenAlex
- W2039029351
- Cited by
- 865
- References
- 42
- Citations by year
- 2026: 55 · 2025: 72 · 2024: 58 · 2023: 54 · 2022: 64 · 2021: 65 · 2020: 73 · 2019: 73 · 2018: 53 · 2017: 62 · 2016: 50 · 2015: 36 · 2014: 45 · 2013: 46 · 2012: 39
- FWCI
- 24.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Open Research (University of Surrey) (submittedVersion)
- Funders
- National Institutes of Health (5p20mh077967-04, DP1OD000579)
- National Institute of Mental Health (P20MH-077967)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Keywords
- local sleep, cortical neuronal activity, slow waves, EEG, wakefulness, prolonged wakefulness, sleep-like state, cognitive impairment, rats, sleep-wake transition
- MeSH terms
- Action Potentials, Animals, Behavior, Animal, Cerebral Cortex, Electroencephalography, Male, Models, Neurological, Rats, Inbred WKY, Reward, Sleep, Sleep Deprivation, Wakefulness, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review