The DOI matches its Crossref record; 68 of the 69 references it cites were found in a registry or an index, and 1 are not checked yet.
Sleep Homeostasis and Cortical Synchronization: II. A Local Field Potential Study of Sleep Slow Waves in the Rat
Open accessAbstract
STUDY OBJECTIVE: Sleep slow-wave activity (SWA, EEG power between 0.5 and 4.0 Hz) decreases homeostatically in the course of non-rapid eye movement sleep (NREM) sleep. According to a recent hypothesis, the homeostatic decrease of sleep SWA is due to a progressive decrease in the strength of corticocortical connections. This hypothesis was evaluated in a large-scale thalamocortical model, which showed that a decrease in synaptic strength, implemented through a reduction of postsynaptic currents, resulted in lower sleep SWA in simulated local field potentials (LFP). The decrease in SWA was associated with a decreased proportion of high-amplitude slow waves, a decreased slope of the slow waves, and an increase in the number of multipeak waves. Here we tested the model predictions by obtaining LFP recordings from the rat cerebral cortex and comparing conditions of high homeostatic sleep pressure (early sleep) and low homeostatic sleep pressure (late sleep). DESIGN: Intracortical LFP recordings during baseline sleep and after 6 hours of sleep deprivation. SETTING: Basic sleep research laboratory. PATIENTS OR PARTICIPANTS: WKY adult male rats. INTERVENTIONS: N/A. MEASUREMENTS AND RESULTS: Early sleep (sleep at the beginning of the major sleep phase, sleep immediately after sleep deprivation) was associated with (1) high SWA, (2) many large slow waves, (3) steep slope of slow waves, and (4) rare occurrence of multipeak waves. By contrast, late sleep (sleep at the end of the major sleep phase, sleep several hours after the end of sleep deprivation) was associated with (1) low SWA, (2) few high-amplitude slow waves, (3) reduced slope of slow waves, and (4) more frequent multipeak waves. CONCLUSION: In rats, changes in sleep SWA are associated with changes in the amplitude and slope of slow waves, and in the number of multi-peak waves. Such changes in slow-wave parameters are compatible with the hypothesis that average synaptic strength decreases in the course of sleep.
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 cited source says what the claim attributes to it.
In the citing paper
“Specifically, the model predicted a decrease in the incidence of high-amplitude slow waves, a decrease in slope, as well as an increase in the number of multipeak waves from early to late sleep, which was con-firmed in related animal and human studies (994, 1269).”
From About Sleep's Role in Memory (2013) · cites this paper as [1269]
In the citing paper
“Recent evidence suggests that slow wave activity is also an indicator of synaptic strength in the brain (Esser et al., 2007; Riedner et al., 2007; Vyazovskiy et al., 2007).”
From Biological rhythms, higher brain function, and behavior: Gaps, opportunities, and challenges (2009) · cites this paper as Vyazovskiy et al., 2007
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
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Two-Process Model of Sleep Regulation
Binder, M. D., Hirokawa, N., & Windhorst, U. (2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_6166 · Cited by 3,900
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
Electric Fields of the Brain: The Neurophysics of EEG
Nunez, P. L., & Harth, E. M. (1982) · Physics Today · doi:10.1063/1.2915137 · Cited by 2,257
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
Learning induces long-term potentiation in the hippocampus
Whitlock, J. R., Heynen, A. J., Shuler, M. G., & Bear, M. F. (2006) · Science · doi:10.1126/science.1128134 · Cited by 1,913
Steriade, M., Nunez, A., & Amzica, F. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03252.1993 · Cited by 1,903
Huber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854
Self-citationElectric Fields of the Brain: The Neurophysics of EEG
Fermaglich, J. (1982) · JAMA · doi:10.1001/jama.1982.03320380071046 · Cited by 1,557
Research works printed but not linked: 1
- [58]Pfister-Genskow M, Cirelli C, Tononi G. Molecular evidence for synaptic potentiation during waking and synaptic downscaling during sleep. Sleep. 2007;30(Abstract Supplement):A5–A6. [Google Scholar]
Cited by
Sorted by citations
Items 101–200 of 225
Pisarenco, I., Caporro, M., Prosperetti, C., & Manconi, M. (2014) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2014.01.002 · Cited by 26
Sleep and Synaptic Homeostasis
Vyazovskiy, V. V., & Faraguna, U. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_301 · Cited by 35
Vyazovskiy, V. V., Palchykova, S., Achermann, P., Tobler, I., & Deboer, T. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx020 · Cited by 23
Hayashi, K., Mukai, N., & Sawa, T. (2013) · Clinical Neurophysiology · doi:10.1016/j.clinph.2013.06.024 · Cited by 25
Microglial TNFα controls daily changes in synaptic GABAARs and sleep slow waves
Pinto, M. J., Bizien, L., Fabre, J. M., Ðukanović, N., Lepetz, V., Henderson, F. J., Pujol, M., Sala, R. W., Tarpin, T., Popa, D., et al. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202401041 · Cited by 29
Encephalopathy related to Status Epilepticus during slow Sleep: a link with sleep homeostasis?
Rubboli, G., Huber, R., Tononi, G., & Tassinari, C. A. (2019) · Epileptic Disorders · doi:10.1684/epd.2019.1059 · Cited by 24
Jaramillo, V., Volk, C., Maric, A., Furrer, M., Fattinger, S., Kurth, S., Lustenberger, C., & Huber, R. (2020) · SLEEP · doi:10.1093/sleep/zsaa038 · Cited by 31
Origin, synchronization, and propagation of sleep slow waves in children
Castelnovo, A., Lividini, A., Riedner, B. A., Avvenuti, G., Jones, S. G., Miano, S., Tononi, G., Manconi, M., & Bernardi, G. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120133 · Cited by 23
Local Gamma Activity During Non-REM Sleep in the Context of Sensory Evoked K-Complexes
Laurino, M., Piarulli, A., Menicucci, D., & Gemignani, A. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01094 · Cited by 18
Effect of prolonged wakefulness on electroencephalographic oscillatory activity during sleep
Olbrich, E., Landolt, H., & Achermann, P. (2013) · Journal of Sleep Research · doi:10.1111/jsr.12123 · Cited by 21
Dopamine D2-receptor Antagonist Droperidol Deepens Sevoflurane Anesthesia
Araki, R., Hayashi, K., & Sawa, T. (2017) · Anesthesiology · doi:10.1097/aln.0000000000002046 · Cited by 20
Galati, S., Salvadè, A., Pace, M., Sarasso, S., Baracchi, F., Bassetti, C. L., Kaelin‐Lang, A., Städler, C., Stanzione, P., & Möller, J. C. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.12.018 · Cited by 19
Sousouri, G., Krugliakova, E., Skoručak, J., Leach, S., Snipes, S., Ferster, M. L., Poian, G. D., Karlen, W., & Huber, R. (2021) · SLEEP · doi:10.1093/sleep/zsab204 · Cited by 21
Zhang, M., Li, R., Wang, Y., & Huang, Z. (2017) · Neural Plasticity · doi:10.1155/2017/5870735 · Cited by 19
Schneider, W. T., Vas, S., Nicol, A. U., & Morton, A. J. (2021) · PLoS ONE · doi:10.1371/journal.pone.0251767 · Cited by 18
Olcese, U., Bos, J. J., Vinck, M., & Pennartz, C. M. A. (2018) · Sleep · doi:10.1093/sleep/zsy167 · Cited by 18
Modulation effect of low-intensity transcranial ultrasound stimulation on REM and NREM sleep
Wang, T., Wang, X., Tian, Y., Gang, W., Li, X., Yan, J., & Yuan, Y. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac413 · Cited by 20
Hayashi, K., Mita, K., & Sawa, T. (2010) · Clinical Neurophysiology · doi:10.1016/j.clinph.2010.03.018 · Cited by 18
How and when EEG reflects changes in neuronal connectivity due to time awake
Snipes, S., Meier, E., Meissner, S. N., Landolt, H., & Huber, R. (2023) · iScience · doi:10.1016/j.isci.2023.107138 · Cited by 19
Sleep and Serotonin Modulate Paracapsular Nitric Oxide Synthase Expressing Neurons of the Amygdala
Bocchio, M., Fisher, S. P., Ünal, G., Ellender, T. J., Vyazovskiy, V. V., & Capogna, M. (2016) · eNeuro · doi:10.1523/eneuro.0177-16.2016 · Cited by 17
Characteristic changes in the slow cortical waves after a 6-h sleep deprivation in rat
Hajnik, T., Tóth, A., & Détári, L. (2013) · Brain Research · doi:10.1016/j.brainres.2012.12.047 · Cited by 17
Vila-Merkle, H., González-Martínez, A., Campos-Jiménez, R., Martínez‐Ricós, J., Teruel‐Martí, V., Blasco‐Serra, A., Lloret, A., Celada, P., & Cervera‐Ferri, A. (2021) · Biomedicines · doi:10.3390/biomedicines9070783 · Cited by 16
Wisor, J. P., Gerashchenko, D., & Kilduff, T. S. (2011) · Current Topics in Medicinal Chemistry · doi:10.2174/156802611797470367 · Cited by 17
Rapid alterations in cortical protein profiles underlie spontaneous sleep and wake bouts
Vazquez, J., Hall, S. C., Witkowska, H. E., & Greco, M. A. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21970 · Cited by 18
The dichotomy between low frequency and delta waves in human sleep: A reappraisal
Lanquart, J., Nardone, P., Hubain, P., Loas, G., & Linkowski, P. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.09.019 · Cited by 15
Slow wave detection in sleeping mice: Comparison of traditional and machine learning methods
Bukhtiyarova, O., Soltani, S., Chauvette, S., & Timofeev, I. (2018) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2018.08.016 · Cited by 14
Thalamic Influence on Slow Wave Slope Renormalization During Sleep
Jaramillo, V., Jendoubi, J., Maric, A., Mensen, A., Heyse, N. C., Eberhard‐Moscicka, A. K., Wiest, R., Bassetti, C. L., & Huber, R. (2021) · Annals of Neurology · doi:10.1002/ana.26217 · Cited by 14
Neurobiology of REM Sleep, NREM Sleep Homeostasis, and Gamma Band Oscillations
McKenna, J. T., Zielinski, M. R., & McCarley, R. W. (2017) · Springer eBooks · doi:10.1007/978-1-4939-6578-6_5 · Cited by 15
Champetier, P., André, C., Rehel, S., Ourry, V., Landeau, B., Mézenge, F., Roquet, D., Vivien, D., Sayette, V. D. L., Chételat, G., et al. (2024) · SLEEP · doi:10.1093/sleep/zsae012 · Cited by 14
van den Munckhof, B., Gefferie, S. R., van Noort, S. A. M., van Teeseling, H. C., Schijvens, M. P., Smit, W., Teunissen, N. W., Plate, J. D. J., Huiskamp, G. J. M., Leijten, F. S. S., et al. (2020) · SLEEP · doi:10.1093/sleep/zsaa088 · Cited by 14
Ascent to moderate altitude impairs overnight memory improvements
Tesler, N., Latshang, T. D., Cascio, C. M. L., Stadelmann, K., Stoewhas, A., Kohler, M., Bloch, K. E., Achermann, P., & Huber, R. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.11.033 · Cited by 13
Spano, G. M., Cavelli, M., Marshall, W., Tononi, G., & Cirelli, C. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15846 · Cited by 11
Local Patterns of Sleep and Wakefulness
Bernardi, G., & Siclari, F. (2019) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-813743-7.00003-7 · Cited by 14
Computational models of memory consolidation and long-term synaptic plasticity during sleep
Rennó‐Costa, C., da Silva, A. C. C., Blanco, W., & Ribeiro, S. T. G. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.10.003 · Cited by 12
Parapatics, S., Anderer, P., Gruber, G., Saletu, B., Saletu-Zyhlarz, G. M., & Dorffner, G. (2015) · Somnologie - Schlafforschung und Schlafmedizin · doi:10.1007/s11818-015-0701-5 · Cited by 11
Carvalho, D. Z., Křemen, V., Mívalt, F., Louis, E. K. S., McCarter, S. J., Bukartyk, J., Przybelski, S. A., Kamykowski, M. G., Spychalla, A. J., Machulda, M. M., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae354 · Cited by 12
Hacking the functions of sleep: noninvasive approaches to stimulate sleep neurophysiology
Krugliakova, E., Breuer, F., Adelhöfer, N., Alonso, A., Besedovsky, L., Murphy, K. R., Peters, E., Raczek, K., Rasch, B., Salvesen, L., et al. (2025) · Physiological Reviews · doi:10.1152/physrev.00007.2025 · Cited by 21
Squarcio, F., Tononi, G., & Cirelli, C. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16460 · Cited by 11
Lafrenière, A., Lina, J., Hernandez, J., Bouchard, M., Gosselin, N., & Carrier, J. (2022) · SLEEP · doi:10.1093/sleep/zsac246 · Cited by 12
Perturbation of Cortical Excitability in a Conditional Model of PCDH19 Disorder
Lamers, D., Landi, S., Mezzena, R., Baroncelli, L., Pillai, V., Cruciani, F., Migliarini, S., Mazzoleni, S., Pasqualetti, M., Passafaro, M., et al. (2022) · Cells · doi:10.3390/cells11121939 · Cited by 10
Olbrich, E., & Achermann, P. (2008) · Journal of Biological Physics · doi:10.1007/s10867-008-9078-z · Cited by 11
Infraslow coordination of slow wave activity through altered neuronal synchrony
Dash, M. B. (2019) · SLEEP · doi:10.1093/sleep/zsz170 · Cited by 9
Marsh, B. M., Navas-Zuloaga, M. G., Rosen, B. Q., Sokolov, Y., Delanois, J. E., Gonzalez, O. C., Krishnan, G. P., Halgren, E., & Bazhenov, M. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012245 · Cited by 10
Gudberg, C., Stevelink, R., Douaud, G., Wulff, K., Lazari, A., Fleming, M. K., & Johansen‐Berg, H. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.745014 · Cited by 10
Detection of neuronal OFF periods as low amplitude neural activity segments
Harding, C. D., Guillaumin, M. C. C., Krone, L. B., Kahn, M. C., Blanco‐Duque, C., Mikutta, C. A., & Vyazovskiy, V. V. (2023) · BMC Neuroscience · doi:10.1186/s12868-023-00780-w · Cited by 7
Association between sleep slow-wave activity and in-vivo estimates of myelin in healthy young men
Deantoni, M., Baillet, M., Hammad, G. H., Berthomier, C., Reyt, M., Jaspar, M., Meyer, C., Egroo, M. V., Talwar, P., Lambot, E., et al. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120045 · Cited by 10
Menicucci, D., Piarulli, A., Allegrini, P., Bedini, R., Bergamasco, M., Laurino, M., Sebastiani, L., & Gemignani, A. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.05.006 · Cited by 9
Wang, Y., Wang, M., Dai, Y., Song, Y., Wang, Y., Lu, B., Li, Y., & Cai, X. (2022) · Micromachines · doi:10.3390/mi13030488 · Cited by 10
Fang, G., Zhang, C., Xia, Y., Lai, Y., Liu, T., You, Z., & Yao, D. (2009) · Physiological Measurement · doi:10.1088/0967-3334/30/7/005 · Cited by 9
Ocampo-Garcés, A., Bassi, A., Brunetti, E. P., Estrada, J. L., & Vivaldi, E. (2020) · SLEEP · doi:10.1093/sleep/zsaa023 · Cited by 9
Szalontai, Ö., Tóth, A., Pethő, M., Keserű, D., Hajnik, T., & Détári, L. (2021) · BMC Neuroscience · doi:10.1186/s12868-021-00619-2 · Cited by 8
Increased cortical involvement and synchronization during CAP A1 slow waves
Ujma, P. P., Halász, P., Simor, P., Fabó, D., & Ferri, R. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1703-4 · Cited by 9
Vaquer-Alicea, A. D. C., Yu, J., Liu, H., & Lucey, B. P. (2023) · SLEEP Advances · doi:10.1093/sleepadvances/zpad047 · Cited by 7
Leemburg, S., Kala, A., Nataraj, A., Karkusova, P., Baindur, S., Suresh, A., Blahna, K., & Jezek, K. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.05.002 · Cited by 10
Local sleep: A new concept in brain plasticity
Avvenuti, G., & Bernardi, G. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00003-5 · Cited by 10
Sleep Slow Oscillations and Cortical Maturation
Kurth, S., & Huber, R. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-384995-3.00010-1 · Cited by 8
Sleep and wake in a model of the thalamocortical system with Martinotti cells
Bugnon, T., Mayner, W. G. P., Cirelli, C., & Tononi, G. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.15836 · Cited by 6
Self-citationCorticothalamic modeling of sleep neurophysiology with applications to mobile electroencephalography
Morshedzadeh, T., Kadak, K., Bastiaens, S. P., Oveisi, M. P., Momi, D., Wang, Z., Harita, S., Jaoude, M. A., Aimone, C., Mann, S., et al. (2025) · SLEEP · doi:10.1093/sleep/zsaf086 · Cited by 7
Plante, D. T., Goldstein, M. R., Cook, J. D., Smith, R., Riedner, B. A., Rumble, M. E., Jelenchick, L. A., Roth, A., Tononi, G., Benca, R. M., et al. (2016) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2016.01.003 · Cited by 6
Multitaper Analysis of Semi-Stationary Spectra From Multivariate Neuronal Spiking Observations
Rupasinghe, A., & Babadi, B. (2020) · IEEE Transactions on Signal Processing · doi:10.1109/tsp.2020.3010197 · Cited by 5
Instrumental learning: An animal model for sleep dependent memory enhancement
Leenaars, C. H. C., Girardi, C. E. N., Joosten, R. N. J. M. A., Lako, I. M., Ruimschotel, E., Hanegraaf, M. A. J., Demattéis, M., Feenstra, M. G. P., & Someren, E. J. W. V. (2013) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2013.04.003 · Cited by 6
Sleep/wake movement velocities, trajectories and micro-arousals during maturation in rats
Gradwohl, G., Olini, N., & Huber, R. (2017) · BMC Neuroscience · doi:10.1186/s12868-017-0343-6 · Cited by 7
NREM Sleep Regulation From Neuronal Assembly to Ion
Gompf, H. S., & Anaclet, C. (2019) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-813743-7.00009-8 · Cited by 6
Human sleep and its regulation
Achermann, P., & Tarokh, L. (2014) · Zurich Open Repository and Archive (University of Zurich) · doi:10.5167/uzh-99785 · Cited by 8
Fasano, A., Biancardi, C., Masi, G., Vecchia, S. D., Frumento, P., Mazzoni, A., Falotico, E., Faraguna, U., & Sicca, F. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.10.057 · Cited by 7
Tóth, A., Traub, M., Bencsik, N., Détári, L., Hajnik, T., & Dobolyi, Á. (2024) · Scientific Reports · doi:10.1038/s41598-024-56392-9 · Cited by 5
Rios, R. L., Green, M., Smith, S. K., Kafashan, M., Ching, S., Farber, N. B., Lin, N., Lucey, B. P., Reynolds, C. F., Lenze, E. J., et al. (2024) · BMJ Open · doi:10.1136/bmjopen-2024-087516 · Cited by 5
Neuroimaging of sleep disorders
Nofzinger, E. A., Maquet, P., & Thorpy, M. J. (2013) · Cambridge University Press eBooks · doi:10.1017/cbo9781139088268.025 · Cited by 5
Neurophysiology of Sleep and Wakefulness
Chellappa, S. L., Schmidt, C., & Cajochen, C. (2014) · Springer eBooks · doi:10.1007/978-88-470-5388-5_3 · Cited by 5
Wang, Y., Liu, J., Gao, F., Xie, W.-Y., Chen, J., Gu, H., Fen, W., Zhong, C., Li, K., Zhuang, S., et al. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.70058 · Cited by 4
Manzella, F. M., Gulvezan, B. F., Maksimovic, S., Useinovic, N., Raol, Y. H., Joksimovic, S. M., Jevtović‐Todorović, V., & Todorovic, S. M. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.703859 · Cited by 4
Skoručak, J., Bölsterli, B. K., Storz, S., Leach, S., Schmitt, B., Ramantani, G., & Huber, R. (2023) · Scientific Reports · doi:10.1038/s41598-023-39984-9 · Cited by 4
Vaudano, A. E., Azzi, N., & Trippi, I. (2019) · Springer eBooks · doi:10.1007/978-3-030-04573-9_10 · Cited by 4
Efficient Implementation of Cerebellar Purkinje Cell With the CORDIC Algorithm on LaCSNN
Hao, X., Yang, S., Wang, J., Deng, B., Wei, X., & Yi, G. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01078 · Cited by 4
Wang, Y., Fan, Z., Wang, M., Liu, J., Xu, S., Lu, Z., Wang, H., Song, Y., Wang, Y., Qu, L., et al. (2021) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2021.3120756 · Cited by 4
The Circadian Clock and the Homeostatic Hourglass: Two Timepieces Controlling Sleep and Wakefulness
Chellappa, S. L., & Cajochen, C. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1262-6_9 · Cited by 5
Perryman, J. I. (2011) · Deep Blue (University of Michigan) · Cited by 4
Theta and alpha EEG oscillations reflect sleep need — except during the wake maintenance zonePreprint
Snipes, S., Meier, E., Meissner, S. N., Landolt, H., & Huber, R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.03.526951 · Cited by 6
Phillips, D. J., Blaine, S., Wallace, N. K., & Karatsoreos, I. N. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1013673 · Cited by 4
Heinrich, B., Schmitt, B., Bölsterli, B. K., Critelli, H., Huber, R., & Fattinger, S. (2020) · Journal of Sleep Research · doi:10.1111/jsr.13137 · Cited by 3
LaGoy, A. D., Kaskie, R. E., Connaboy, C., Germain, A., & Ferrarelli, F. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2020.12.013 · Cited by 3
Author's reply to “Cerebral metabolism and sleep homeostasis: A comment on Vyazovskiy et al.”
Vyazovskiy, V. V., Tobler, I., Cirelli, C., & Tononi, G. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2009.08.003 · Cited by 3
Vyazovskiy, V. V., Olcese, U., & Tononi, G. (2011) · Neuromethods · doi:10.1007/7657_2011_22 · Cited by 2
Cortical zeta-inhibitory peptide injection reduces local sleep need
Carroll, C. M., Hsiang, H. W., Snyder, S., Forsberg, J., & Dash, M. B. (2019) · SLEEP · doi:10.1093/sleep/zsz028 · Cited by 2
Sleep and Waking Across the Life Span
Huber, R., & Tononi, G. (2009) · Wiley eBooks · doi:10.1002/9780470478509.neubb001025 · Cited by 2
Microglial TNFα controls synaptic GABAARs, sleep slow waves and memory consolidationPreprint
Pinto, M. J., Bizien, L., Fabre, J. M., Ðukanović, N., Lepetz, V., Henderson, F., Pujol, M., Sala, R. W., Tarpin, T., Popa, D., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.21.481254 · Cited by 2
Oscillatory-Quality of sleep spindles: from properties to functionPreprint
Blanco-Duque, C., Bond, S. A., Krone, L., Dufour, J.-P., Gillen, E. C. P., Kahn, M., Purple, R., Bannerman, D., Mann, E., Achermann, P., et al. (2023) · bioRxiv · doi:10.1101/2023.06.28.546981 · Cited by 2
LPS-induced sepsis disrupts brain activity in a region- and vigilance-state specific mannerPreprint
Leemburg, S., Kala, A., Nataraj, A., Karkusova, P., Baindur, S., Suresh, A., Blahna, K., & Jezek, K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.25.630319 · Cited by 2
Contrasting effects of global and local cortical activity on the regulation of sleepPreprint
Krone, L. B., Hamilton, J. D., Hoerder‐Suabedissen, A., Marnitz, C. R. V., Memis, L., Szabo, A. B., Akerman, C. J., Molnár, Z., & Vyazovskiy, V. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.07.673922 · Cited by 6
Evaluation and Management in Patients with Obstructive Sleep Apnea
Дєєва, Ю., & Naumenko, O. M. (2023) · IntechOpen eBooks · doi:10.5772/intechopen.1002896 · Cited by 1
Sleep phenotyping in a rat model of susceptibility to substance use disorders
Ficiarà, E., Faniyan, O. O., Simayi, R., Gallo, F. D., Roberto, M., Ciccocioppo, R., Bellesi, M., & de Vivo, L. (2025) · PLoS ONE · doi:10.1371/journal.pone.0324459 · Cited by 1
Ventura, S., Ryan, M. A., Mathieson, S., Livingstone, V., O’Toole, J. M., & Boylan, G. B. (2025) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2025.114728 · Cited by 1
Martinez, C., de Sousa, B. M., Carmo, F. D. A. C., Zacharias, L. R., Leite, J. P., Diba, K., & Lopes‐Aguiar, C. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf287 · Cited by 2
Rhythms and Background (RnB): The Spectroscopy of Sleep Recordings
Dubé, J., Fóti, M., Jaffard, S., Latreille, V., Frauscher, B., Carrier, J., & Lina, J.-M. (2026) · eNeuro · doi:10.1523/eneuro.0235-25.2025 · Cited by 1
Sleep Oscillations and Psychiatric Disorders
Ferrarelli, F., & Tononi, G. (2020) · Springer eBooks · doi:10.1007/978-1-0716-0653-7_9 · Cited by 1
Cerebral Gray Matter May Not Explain Sleep Slow-Wave Characteristics after Severe Brain Injury
Kalantari, N., Daneault, V., Blais, H., André, C., Sanchez, E., Lina, J., Arbour, C., Gilbert, D., Carrier, J., & Gosselin, N. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1306-23.2024 · Cited by 2
Local infrared stimulation modulates spontaneous cortical slow wave dynamics in anesthetized rats
Szabó, Á., Fiáth, R., Horváth, Á. C., Barthó, P., Ulbert, I., & Fekete, Z. (2026) · Scientific Reports · doi:10.1038/s41598-026-38781-4 · Cited by 1
The Comodulation Measure of Neuronal Oscillations
Li, D., & Xiaoli Li, A. (2016) · Springer eBooks · doi:10.1007/978-981-10-1822-0_11 · Cited by 1
Peters, S. E. (2017) · doi:10.7282/t35142bt · Cited by 1
Analyse de l'activité en ondes lentes et des oscillations lentes chez les somnambules
Perrault, R. (2014) · doi:10.71781/18286 · Cited by 1
Metadata
- Authors
- Vyazovskiy, V. V., Riedner, B. A., Cirelli, C., & Tononi, G.
- Affiliations
- University of Wisconsin–Madison (US)
- Venue
- SLEEP
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-12
- Volume
- 30
- Issue
- 12
- Pages
- 1631-1642
- ISSN
- 0161-8105 (ISSN-L)
- 1550-9109
- PMC
- PMC2276140
- OpenAlex
- W2124761808
- Cited by
- 225
- References
- 68
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 14 · 2023: 15 · 2022: 11 · 2021: 12 · 2020: 11 · 2019: 13 · 2018: 14 · 2017: 16 · 2016: 16 · 2015: 10 · 2014: 19 · 2013: 18 · 2012: 6
- FWCI
- 4.17
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- SLEEP (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Open Research (University of Surrey) (submittedVersion)
- Surrey Research Insight Open Access (The University of Surrey) (submittedVersion)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (106264)
- National Institutes of Health (NRSA T32)
- National Institute of General Medical Sciences (T32GM007507)
- National Institute of Diabetes and Digestive and Kidney Diseases (T90DK070079)
- 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
- sleep homeostasis, sleep slow waves, cortical synchronization, synaptic efficacy, sleep deprivation, NREM sleep, thalamocortical model, local field potentials, corticocortical connections, rat cortex
- MeSH terms
- Animals, Cerebral Cortex, Circadian Rhythm, Computer Simulation, Cortical Synchronization, Electroencephalography, Evoked Potentials, Fourier Analysis, Homeostasis, Male, Nerve Net, Rats, Inbred WKY, Sleep, Sleep Deprivation, Thalamus, 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