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Sleep Loss Can Cause Death through Accumulation of Reactive Oxygen Species in the Gut
Open accessAbstract
The view that sleep is essential for survival is supported by the ubiquity of this behavior, the apparent existence of sleep-like states in the earliest animals, and the fact that severe sleep loss can be lethal. The cause of this lethality is unknown. Here we show, using flies and mice, that sleep deprivation leads to accumulation of reactive oxygen species (ROS) and consequent oxidative stress, specifically in the gut. ROS are not just correlates of sleep deprivation but drivers of death: their neutralization prevents oxidative stress and allows flies to have a normal lifespan with little to no sleep. The rescue can be achieved with oral antioxidant compounds or with gut-targeted transgenic expression of antioxidant enzymes. We conclude that death upon severe sleep restriction can be caused by oxidative stress, that the gut is central in this process, and that survival without sleep is possible when ROS accumulation is prevented. VIDEO ABSTRACT.
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In the citing paper
“severe sleep loss causes accumulation of ROS in the gut (but not the brain) of both flies and mice, which was associated with death of the flies”
From Effects of Coffee and Its Components on the Gastrointestinal Tract and the Brain–Gut Axis (2020) · cites this paper as [225]
In the citing paper
“all these effects could be prevented by oral administration of antioxidant compounds or through gut-targeted transgenic expression of antioxidant enzymes.”
From Effects of Coffee and Its Components on the Gastrointestinal Tract and the Brain–Gut Axis (2020) · cites this paper as [225]
In the citing paper
“the antioxidant components of coffee (like melatonin, one of the antioxidant compounds used in the mentioned study by Rogulja and collaborators, [225]) may prevent accumulation of ROS in the gut and avoid the deleterious effect of voluntary sleep restriction.”
From Effects of Coffee and Its Components on the Gastrointestinal Tract and the Brain–Gut Axis (2020) · cites this paper as [225]
In the citing paper
“sleep deprivation caused mice and flies death through the accumulation of reactive oxygen species (ROS) in the gut [20]”
From Healthy Human Fecal Microbiota Transplantation into Mice Attenuates MPTP-Induced Neurotoxicity via AMPK/SOD2 Pathway (2023) · cites this paper as [20]
Citations
Cites
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
Brand, A. H., & Perrimon, N. (1993) · Development · doi:10.1242/dev.118.2.401 · Cited by 9,510
ROS function in redox signaling and oxidative stress
Schieber, M., & Chandel, N. S. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.034 · Cited by 6,931
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139
Rogakou, E. P., Pilch, D. R., Orr, A. H., Ivanova, V. S., & Bonner, W. M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.10.5858 · Cited by 5,438
Sleep Drives Metabolite Clearance from the Adult Brain
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., O’Donnell, J., Christensen, D. J., Nicholson, C., Iliff, J. J., et al. (2013) · Science · doi:10.1126/science.1241224 · Cited by 5,411
Role of nrf2 in oxidative stress and toxicity
Ma, Q. (2013) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-011112-140320 · Cited by 4,903
Reactive Oxygen Species in Inflammation and Tissue Injury
Mittal, M., Siddiqui, M. R., Tran, K., Reddy, S. P., & Malik, A. B. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.5149 · Cited by 4,897
Mitochondria, Oxidants, and Aging
Balaban, R. S., Nemoto, S., & Finkel, T. (2005) · Cell · doi:10.1016/j.cell.2005.02.001 · Cited by 4,388
Activation of apoptosis signalling pathways by reactive oxygen species
Redza-Dutordoir, M., & Averill-Bates, D. A. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.09.012 · Cited by 3,731
ROS as signalling molecules: Mechanisms that generate specificity in ROS homeostasis
D'Autréaux, B., & Toledano, M. B. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2256 · Cited by 3,642
Mittler, R. (2017) · Trends in Plant Science · doi:10.1016/j.tplants.2016.08.002 · Cited by 3,499
Lee, T., & Luo, L. (1999) · Neuron · doi:10.1016/s0896-6273(00)80701-1 · Cited by 2,540
Oxidative Stress: An Essential Factor in the Pathogenesis of Gastrointestinal Mucosal Diseases
Bhattacharyya, A., Chattopadhyay, R., Mitra, S., & Crowe, S. E. (2014) · Physiological Reviews · doi:10.1152/physrev.00040.2012 · Cited by 2,484
Exercise-Induced Oxidative Stress: Cellular Mechanisms and Impact on Muscle Force Production
Powers, S. K., & Jackson, M. J. (2008) · Physiological Reviews · doi:10.1152/physrev.00031.2007 · Cited by 2,459
Megabase Chromatin Domains Involved in DNA Double-Strand Breaks in Vivo
Rogakou, E. P., Boon, C., Redon, C., & Bonner, W. M. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.5.905 · Cited by 2,422
Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life
Halliwell, B. B. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.077073 · Cited by 2,402
Tononi, G., & Cirelli, C. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.025 · Cited by 2,356
The expensive-tissue hypothesis: The brain and the digestive system in human and primate evolution
Aiello, L. C., & Wheeler, P. (1995) · Current Anthropology · doi:10.1086/204350 · Cited by 2,291
Transcriptional Regulation by Nrf2
Tonelli, C., Chio, I. I. C., & Tuveson, D. A. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7342 · Cited by 2,280
Oxidative stress and autophagy: The clash between damage and metabolic needs
Filomeni, G., De Zio, D., & Cecconi, F. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.150 · Cited by 2,195
Cellular mechanisms and physiological consequences of redox-dependent signalling
Holmström, K. M., & Finkel, T. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3801 · Cited by 2,093
Molecular Basis of Colorectal Cancer
Markowitz, S. D., & Bertagnolli, M. M. (2009) · New England Journal of Medicine · doi:10.1056/nejmra0804588 · Cited by 2,052
The microbiome and innate immunity
Thaiss, C. A., Zmora, N., Levy, M., & Elinav, E. (2016) · Nature · doi:10.1038/nature18847 · Cited by 2,012
Inflammation-induced cancer: Crosstalk between tumours, immune cells and microorganisms
Elinav, E., Nowarski, R., Thaiss, C. A., Hu, B., Jin, C., & Flavell, R. A. (2013) · Nature reviews. Cancer · doi:10.1038/nrc3611 · Cited by 2,000
Stem Cells, Self-Renewal, and Differentiation in the Intestinal Epithelium
van der Flier, L. G., & Clevers, H. C. (2008) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163145 · Cited by 1,994
Free radical-mediated oxidation of free amino acids and amino acid residues in proteins
Stadtman, E. R., & Levine, R. L. (2003) · Amino Acids · doi:10.1007/s00726-003-0011-2 · Cited by 1,968
RIP3, an Energy Metabolism Regulator That Switches TNF-Induced Cell Death from Apoptosis to Necrosis
Zhang, D.-W., Shao, J., Lin, J., Zhang, N., Lu, B.-J., Lin, S.-C., Dong, M.-Q., & Han, J. (2009) · Science · doi:10.1126/science.1172308 · Cited by 1,931
Short- and long-term health consequences of sleep disruption
Medic, G., Wille, M., & Hemels, M. (2017) · Nature and Science of Sleep · doi:10.2147/nss.s134864 · Cited by 1,776
Dysbiosis and the immune system
Levy, M., Kolodziejczyk, A. A., Thaiss, C. A., & Elinav, E. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.7 · Cited by 1,769
Jones, D. P. (2006) · Antioxidants & Redox Signaling · doi:10.1089/ars.2006.8.1865 · Cited by 1,726
Eukaryotic Stress Granules: The Ins and Outs of Translation
Buchan, J. R., & Parker, R. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.11.020 · Cited by 1,535
A GAL4-Driver Line Resource for Drosophila Neurobiology
Jenett, A., Rubin, G. M., Ngo, T.-T. B., Shepherd, D., Murphy, C., Dionne, H., Pfeiffer, B. D., Cavallaro, A., Hall, D., Jeter, J., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.011 · Cited by 1,449
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 · cited 1×
“This idea is supported by the significant cognitive decline noticeable after sleep loss (Donlea, 2019; Killgore, 2010; Krause et al., 2017).”
Endoplasmic Reticulum Stress and Oxidative Stress in Cell Fate Decision and Human Disease
Cao, S. S., & Kaufman, R. J. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5851 · Cited by 1,393
Oxidative DNA damage and disease: induction, repair and significance
Evans, M. D., Dizdaroglu, M., & Cooke, M. S. (2004) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2003.11.001 · Cited by 1,372
Superoxide Anion Radical (O·̄2), Superoxide Dismutases, and Related Matters
Fridovich, I. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.18515 · Cited by 1,337
Correlates of Sleep and Waking in Drosophila melanogaster
Shaw, P. J., Cirelli, C., Greenspan, R. J., & Tononi, G. (2000) · Science · doi:10.1126/science.287.5459.1834 · Cited by 1,300
The measurement and mechanism of lipid peroxidation in biological systems
Gutteridge, J. M. C., & Halliwell, B. B. (1990) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(90)90206-q · Cited by 1,297
Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines
Rea, I. M., Gibson, D. S., McGilligan, V., McNerlan, S. E., Alexander, H. D., & Ross, O. A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00586 · Cited by 1,267
Molecular inflammation: Underpinnings of aging and age-related diseases
Chung, H. Y., Cesari, M., Anton, S., Marzetti, E., Giovannini, S., Seo, A. Y., Carter, C., Yu, B. P., & Leeuwenburgh, C. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2008.07.002 · Cited by 1,203
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
Refinement of Tools for Targeted Gene Expression in Drosophila
Pfeiffer, B. D., Ngo, T.-T. B., Hibbard, K. L., Murphy, C., Jenett, A., Truman, J. W., & Rubin, G. M. (2010) · Genetics · doi:10.1534/genetics.110.119917 · Cited by 1,153
NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates
Luquet, S. H., Perez, F. A., Hnasko, T. S., & Palmiter, R. D. (2005) · Science · doi:10.1126/science.1115524 · Cited by 1,150
Evidence that stem cells reside in the adult Drosophila midgut epithelium
Micchelli, C. A., & Perrimon, N. (2005) · Nature · doi:10.1038/nature04371 · Cited by 1,139
Sleep and inflammation: partners in sickness and in health
Irwin, M. R. (2019) · Nature reviews. Immunology · doi:10.1038/s41577-019-0190-z · Cited by 1,138
Antioxidant responses and cellular adjustments to oxidative stress
Espinosa‐Díez, C., Miguel, V., Mennerich, D., Kietzmann, T., Sánchez-Pérez, P., Cadenas, S., & Lamas, S. (2015) · Redox Biology · doi:10.1016/j.redox.2015.07.008 · Cited by 1,125
The adult Drosophila posterior midgut is maintained by pluripotent stem cells
Ohlstein, B., & Spradling, A. C. (2005) · Nature · doi:10.1038/nature04333 · Cited by 1,089
An internal thermal sensor controlling temperature preference in Drosophila
Hamada, F. N., Rosenzweig, M. R., Kang, K., Pulver, S. R., Ghezzi, A., Jegla, T. J., & Garrity, P. (2008) · Nature · doi:10.1038/nature07001 · Cited by 1,089
Rest in Drosophila is a sleep-like state
Hendricks, J. C., Finn, S. M., Panckeri, K. A., Chavkin, J., Williams, J. A., Sehgal, A., & Pack, A. I. (2000) · Neuron · doi:10.1016/s0896-6273(00)80877-6 · Cited by 1,050
The Global Problem of Insufficient Sleep and Its Serious Public Health Implications
Chattu, V. K., Manzar, M. D., Kumary, S., Burman, D., Spence, D. W., & Pandi-Perumal, S. R. (2018) · Healthcare · doi:10.3390/healthcare7010001 · Cited by 1,028
Cytokine/Jak/Stat Signaling Mediates Regeneration and Homeostasis in the Drosophila Midgut
Jiang, H., Patel, P. H., Kohlmaier, A., Grenley, M. O., McEwen, D. G., & Edgar, B. A. (2009) · Cell · doi:10.1016/j.cell.2009.05.014 · Cited by 1,017
Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species
Chen, X., Tian, X., Shin, I., & Yoon, J. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15037e · Cited by 980
Endoplasmic Reticulum Stress and Associated ROS
Zeeshan, H. M. A., Lee, K. H., Kim, H., & Chae, H. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030327 · Cited by 976
Wagh, D. A., Rasse, T. M., Asan, E., Hofbauer, A., Schwenkert, I., Dürrbeck, H., Buchner, S., Dabauvalle, M.-C., Schmidt, M., Qin, G., et al. (2006) · Neuron · doi:10.1016/j.neuron.2006.02.008 · Cited by 908
DNA Base Damage by Reactive Oxygen Species, Oxidizing Agents, and UV Radiation
Cadet, J., & Wagner, J. R. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012559 · Cited by 903
Why neurodegenerative diseases are progressive: uncontrolled inflammation drives disease progression
Gao, H., & Hong, J. (2008) · Trends in Immunology · doi:10.1016/j.it.2008.05.002 · Cited by 852
Detection of picomole levels of hydroperoxides using a fluorescent dichlorofluorescein assay
Cathcart, R., Schwiers, E., & Ames, B. N. (1983) · Analytical Biochemistry · doi:10.1016/0003-2697(83)90270-1 · Cited by 851
A Direct Role for Dual Oxidase in Drosophila Gut Immunity
Ha, E.-M., Oh, C.-T., Bae, Y. S., & Lee, W. (2005) · Science · doi:10.1126/science.1117311 · Cited by 849
Night-Shift Work and Risk of Colorectal Cancer in the Nurses' Health Study
Schernhammer, E. S., Laden, F., Speizer, F. E., Willett, W. C., Hunter, D. J., Kawachi, I. I., Fuchs, C. S., & Colditz, G. A. (2003) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/95.11.825 · Cited by 837
Animal sleep: A review of sleep duration across phylogeny
Campbell, S. S., & Tobler, I. (1984) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(84)90054-x · Cited by 832
Buchon, N. S., Broderick, N. A., Poidevin, M., Pradervand, S., & Lemaître, B. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.01.003 · Cited by 824
The sleep-wake cycle regulates brain interstitial fluid tau in mice and CSF tau in humans
Holth, J. K., Fritschi, S. K., Wang, C., Pedersen, N. P., Cirrito, J. R., Mahan, T. E., Finn, M. B., Manis, M., Geerling, J. C., Fuller, P. M., et al. (2019) · Science · doi:10.1126/science.aav2546 · Cited by 813
Impact of insufficient sleep on total daily energy expenditure, food intake, and weight gain
Markwald, R. R., Melanson, E. L., Smith, M. R., Higgins, J., Perreault, L., Eckel, R. H., & Wright, K. P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216951110 · Cited by 810
Reactive oxygen species prime Drosophila haematopoietic progenitors for differentiation
Owusu-Ansah, E., & Banerjee, U. (2009) · Nature · doi:10.1038/nature08313 · Cited by 742
Buchon, N., Broderick, N. A., Chakrabarti, S., & Lemaître, B. (2009) · Genes & Development · doi:10.1101/gad.1827009 · Cited by 722
Melatonin as a Potent and Inducible Endogenous Antioxidant: Synthesis and Metabolism
Tan, D.-X., Manchester, L., Esteban-Zubero, E., Zhou, Z., & Reiter, R. (2015) · Molecules · doi:10.3390/molecules201018886 · Cited by 719
Keap1/Nrf2 Signaling Regulates Oxidative Stress Tolerance and Lifespan in Drosophila
Sykiotis, G. P., & Bohmann, D. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.12.002 · Cited by 660
REVIEW: Gastrointestinal Melatonin: Localization, Function, and Clinical Relevance
Bubenik, G. A. (2002) · Digestive Diseases and Sciences · doi:10.1023/a:1020107915919 · Cited by 655
Extensive and divergent effects of sleep and wakefulness on brain gene expression
Cirelli, C., Gutierrez, C. M., & Tononi, G. (2004) · Neuron · doi:10.1016/s0896-6273(03)00814-6 · Cited by 627
Inflammatory Mechanisms: The Molecular Basis of Inflammation and Disease
Libby, P. (2008) · Nutrition Reviews · doi:10.1111/j.1753-4887.2007.tb00352.x · Cited by 625
Rera, M., Clark, R. I., & Walker, D. W. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215849110 · Cited by 619
Layered reward signalling through octopamine and dopamine in Drosophila
Burke, C. J., Huetteroth, W., Owald, D., Perisse, E., Krashes, M. J., Das, G., Gohl, D., Silies, M., Certel, S., & Waddell, S. (2012) · Nature · doi:10.1038/nature11614 · Cited by 614
Dopamine Is a Regulator of Arousal in the Fruit Fly
Kume, K., Kume, S., Park, S. K., Hirsh, J., & Jackson, F. R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2048-05.2005 · Cited by 605
XBP-1 Is a Cell-Nonautonomous Regulator of Stress Resistance and Longevity
Taylor, R. C., & Dillin, A. G. (2013) · Cell · doi:10.1016/j.cell.2013.05.042 · Cited by 585
JNK Activity in Somatic Stem Cells Causes Loss of Tissue Homeostasis in the Aging Drosophila Gut
Biteau, B., Hochmuth, C. E., & Jasper, H. (2008) · Cell Stem Cell · doi:10.1016/j.stem.2008.07.024 · Cited by 583
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
Santos, C. X. C., Tanaka, L. Y., Wosniak, J., & Laurindo, F. R. M. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2009.2625 · Cited by 572
Inflammatory mechanisms: the molecular basis of inflammation and disease
Libby, P. (2007) · Nutrition Reviews · doi:10.1301/nr.2007.dec.s140-s146 · Cited by 560
Tissue Damage-Induced Intestinal Stem Cell Division in Drosophila
Amcheslavsky, A., Jiang, J., & Ip, Y. T. (2009) · Cell stem cell · doi:10.1016/j.stem.2008.10.016 · Cited by 548
Genetic mosaic with dual binary transcriptional systems in Drosophila
Lai, S.-L., & Lee, T. (2006) · Nature Neuroscience · doi:10.1038/nn1681 · Cited by 547
Mullington, J. M., Simpson, N. S., Meier-Ewert, H. K., & Haack, M. (2010) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1016/j.beem.2010.08.014 · Cited by 519
Homer1a drives homeostatic scaling-down of excitatory synapses during sleep
Diering, G. H., Nirujogi, R. S., Roth, R. H., Worley, P. F., Pandey, A., & Huganir, R. L. (2017) · Science · doi:10.1126/science.aai8355 · Cited by 516
Morphological and Molecular Characterization of Adult Midgut Compartmentalization in Drosophila
Buchon, N., Osman, D., David, F. P. A., Fang, H. Y., Boquete, J., Deplancke, B., & Lemaître, B. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.04.001 · Cited by 515
Clark, R. I., Salazar, A., Yamada, R., Fitz-Gibbon, S., Morselli, M., Alcaraz, J., Rana, A., Rera, M., Pellegrini, M., Ja, W. W., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.08.004 · Cited by 510
Inflammatory networks underlying colorectal cancer
Lasry, A., Zinger, A., & Ben‐Neriah, Y. (2016) · Nature Immunology · doi:10.1038/ni.3384 · Cited by 497
Anatomy and Physiology of the Digestive Tract of Drosophila melanogaster
Miguel-Aliaga, I., Jasper, H., & Lemaitre, B. (2018) · Genetics · doi:10.1534/genetics.118.300224 · Cited by 491
Stress response genes protect against lethal effects of sleep deprivation in Drosophila
Shaw, P. J., Tononi, G., Greenspan, R. J., & Robinson, D. F. (2002) · Nature · doi:10.1038/417287a · Cited by 488
Physiological Correlates of Prolonged Sleep Deprivation in Rats
Rechtschaffen, A., Gilliland, M. A., Bergmann, B. M., & Winter, J. B. (1983) · Science · doi:10.1126/science.6857280 · Cited by 487
Poroyko, V. A., Carreras, A., Khalyfa, A., Khalyfa, A. A., Leone, V., Peris, E., Almendros, I., Gileles-Hillel, A., Qiao, Z., Hubert, N., et al. (2016) · Scientific Reports · doi:10.1038/srep35405 · Cited by 480 · cited 1×
“This might be relevant because sleep deprivation reportedly affects gut microbiota (Benedict et al., 2016; El Aidy et al., 2019; Gao et al., 2019; Ma et al., 2019; Poroyko et al., 2016), but conflicting evidence exists (Zhang et al.”
Reduced sleep in Drosophila Shaker mutants
Cirelli, C., Bushey, D., Hill, S., Huber, R., Kreber, R. A., Ganetzky, B., & Tononi, G. (2005) · Nature · doi:10.1038/nature03486 · Cited by 474
Modulation of longevity and tissue homeostasis by the Drosophila PGC-1 homolog
Rera, M., Bahadorani, S., Cho, J., Koehler, C. L., Ulgherait, M., Hur, J. H., Ansari, W. S., Lo, T., Jones, D. L., & Walker, D. W. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.09.013 · Cited by 472
Oxidative Stress, Redox Signaling, and Autophagy: Cell Death Versus Survival
Navarro-Yepes, J., Burns, M., Anandhan, A., Khalimonchuk, O., Razo, L. M. D., Quintanilla‐Vega, B., Pappa, A., Panayiotidis, M. I., & Franco, R. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5837 · Cited by 467
Sleep modulates haematopoiesis and protects against atherosclerosis
McAlpine, C. S., Kiss, M. G., Rattik, S., He, S., Vassalli, A., Valet, C., Anzai, A., Chan, C. T., Mindur, J. E., Kahles, F., et al. (2019) · Nature · doi:10.1038/s41586-019-0948-2 · Cited by 447
Sleep function: Toward elucidating an enigma
Krueger, J. M., Frank, M. G., Wisor, J. P., & Roy, S. (2016) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.08.005 · Cited by 440
Regulation of life span by the gut microbiota in the short-lived African turquoise killifish
Smith, P., Willemsen, D., Popkes, M., Metge, F., Gandiwa, E., Reichard, M., & Valenzano, D. R. (2017) · eLife · doi:10.7554/elife.27014 · Cited by 423
Sleep Homeostasis in Drosophila Melanogaster
Huber, R., Hill, S., Holladay, C., Biesiadecki, M., Tononi, G., & Cirelli, C. (2004) · SLEEP · doi:10.1093/sleep/27.4.628 · Cited by 412
Jones, R. M., Luo, L., Ardita, C., Richardson, A. N., Kwon, Y. M., Mercante, J. W., Alam, A. M., Gates, C. L., Wu, H., Swanson, P. A., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.224 · Cited by 409
Lee, K.-A., Kim, S.-H., Kim, E. K., Ha, E.-M., You, H., Kim, B., Kim, M., Kwon, Y., Ryu, J.-H., & Lee, W. (2013) · Cell · doi:10.1016/j.cell.2013.04.009 · Cited by 406
Hardeland, R., & Pöeggeler, B. (2003) · Journal of Pineal Research · doi:10.1034/j.1600-079x.2003.00040.x · Cited by 400
Functions 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
The impact of sleep deprivation on food desire in the human brain
Greer, S. M., Goldstein, A. N., & Walker, M. P. (2013) · Nature Communications · doi:10.1038/ncomms3259 · Cited by 375
Redox Regulation by Keap1 and Nrf2 Controls Intestinal Stem Cell Proliferation in Drosophila
Hochmuth, C. E., Biteau, B., Bohmann, D., & Jasper, H. (2011) · Cell stem cell · doi:10.1016/j.stem.2010.12.006 · Cited by 374
Cirelli, C., & Tononi, G. (2000) · Brain Research · doi:10.1016/s0006-8993(00)03008-0 · Cited by 372
Lifespan Extension by Preserving Proliferative Homeostasis in Drosophila
Biteau, B., Karpac, J., Supoyo, S., DeGennaro, M., Lehmann, R., & Jasper, H. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001159 · Cited by 363
Widespread Changes in Synaptic Markers as a Function of Sleep and Wakefulness in Drosophila
Gilestro, G. F., Tononi, G., & Cirelli, C. (2009) · Science · doi:10.1126/science.1166673 · Cited by 360
Sleep and Synaptic Homeostasis: Structural Evidence in Drosophila
Bushey, D., Tononi, G., & Cirelli, C. (2011) · Science · doi:10.1126/science.1202839 · Cited by 357
Short sleep duration and cardiometabolic risk: from pathophysiology to clinical evidence
Tobaldini, E., Fiorelli, E. M., Solbiati, M., Costantino, G., Nobili, L., & Montano, N. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0109-6 · Cited by 357
Ha, E.-M., Lee, K.-A., Seo, Y. Y., Kim, S.-H., Lim, J.-H., Oh, B., Kim, J., & Lee, W. (2009) · Nature Immunology · doi:10.1038/ni.1765 · Cited by 349
Identification of SLEEPLESS, a sleep-promoting factor
Koh, K., Joiner, W. J., Wu, M. N., Yue, Z., Smith, C. J., & Sehgal, A. (2008) · Science · doi:10.1126/science.1155942 · Cited by 347
Sleep Deprivation in the Rat: III. Total Sleep Deprivation
Everson, C. A., Bergmann, B. M., & Rechtschaffen, A. (1989) · SLEEP · doi:10.1093/sleep/12.1.13 · Cited by 341
A dynamic role for the mushroom bodies in promoting sleep in Drosophila
Pitman, J. L., McGill, J. J., Keegan, K. P., & Allada, R. (2006) · Nature · doi:10.1038/nature04739 · Cited by 330
Benedict, C., Vogel, H., Jonas, W., Woting, A., Blaut, M., Schürmann, A., & Cedernaes, J. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.10.003 · Cited by 324 · cited 1×
“This might be relevant because sleep deprivation reportedly affects gut microbiota (Benedict et al., 2016; El Aidy et al., 2019; Gao et al., 2019; Ma et al., 2019; Poroyko et al., 2016), but conflicting evidence exists (Zhang et al.”
AMPK Modulates Tissue and Organismal Aging in a Non-Cell-Autonomous Manner
Ulgherait, M., Rana, A., Rera, M., Graniel, J. V., & Walker, D. W. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.006 · Cited by 320
Sleep Drive Is Encoded by Neural Plastic Changes in a Dedicated Circuit
Liu, S., Liu, Q., Tabuchi, M., & Wu, M. N. (2016) · Cell · doi:10.1016/j.cell.2016.04.013 · Cited by 317
Large colonial organisms with coordinated growth in oxygenated environments 2.1 Gyr ago
Albani, A. E., Bengtson, S., Canfield, D. E., Bekker, A., Macchiarelli, R., Mazurier, A., Hammarlund, E. U., Boulvais, P., Dupuy, J.-J., Fontaine, C., et al. (2010) · Nature · doi:10.1038/nature09166 · Cited by 316
Role of hippocampal oxidative stress in memory deficits induced by sleep deprivation in mice
Silva, R. H., Abílio, V. C., Takatsu, A. L., Kameda, S. R., Grassl, C., Chehin, A. B., Medrano, W. A., Calzavara, M. B., Registro, S., Andersen, M. L., et al. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2003.11.032 · Cited by 307
Sleep Deprivation and Oxidative Stress in Animal Models: A Systematic Review
Villafuerte, G., Miguel‐Puga, J. A., Rodríguez, E. M., Machado, S. E. D. C., Manjarrez, E., & Arias-Carrión, Ó. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/234952 · Cited by 305
Role of melatonin in sleep deprivation‐induced intestinal barrier dysfunction in mice
Gao, T., Wang, Z., Dong, Y., Cao, J., Lin, R., Wang, X., Yu, Z., & Chen, Y. (2019) · Journal of Pineal Research · doi:10.1111/jpi.12574 · Cited by 301
Direct and indirect antioxidant properties of α‐lipoic acid and therapeutic potential
Rochette, L., Ghibu, S., Richard, C., Zeller, M., Cottin, Y., & Vergely, C. (2013) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201200608 · Cited by 297
Life extension in Drosophila by feeding a drug
Kang, H.-L., Benzer, S., & Min, K. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.022631999 · Cited by 294
Two Dopaminergic Neurons Signal to the Dorsal Fan-Shaped Body to Promote Wakefulness in Drosophila
Liu, Q., Liu, S., Kodama, L., Driscoll, M. R., & Wu, M. N. (2012) · Current Biology · doi:10.1016/j.cub.2012.09.008 · Cited by 288
Madigan, J. P. (2002) · Nucleic Acids Research · doi:10.1093/nar/gkf496 · Cited by 287
ROS in gastrointestinal inflammation: Rescue Or Sabotage?
Aviello, G., & Knaus, U. G. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13428 · Cited by 284
Double strand break repair functions of histone H2AX
Scully, R., & Xie, A. (2013) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2013.07.007 · Cited by 277
Redox signaling in the gastrointestinal tract
Pérez, S., Taléns‐Visconti, R., Rius‐Pérez, S., Finamor, I., & Sastre, J. (2017) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.12.048 · Cited by 277
Electrophysiological Correlates of Rest and Activity in Drosophila melanogaster
Nitz, D. A., van Swinderen, B., Tononi, G., & Greenspan, R. J. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01300-3 · Cited by 276
Control and dysregulation of redox signalling in the gastrointestinal tract
Campbell, E. L., & Colgan, S. P. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0079-5 · Cited by 267
Age‐related changes in Drosophila midgut are associated with PVF2, a PDGF/VEGF‐like growth factor
Choi, N., Kim, J., Yang, D., Kim, Y., & Yoo, M. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00380.x · Cited by 256
Sleep deprivation decreases superoxide dismutase activity in rat hippocampus and brainstem
Ramanathan, L., Gulyani, S., Nienhuis, R., & Siegel, J. M. (2002) · Neuroreport · doi:10.1097/00001756-200208070-00007 · Cited by 254
The free radical flux theory of sleep
Reimund, E. (1994) · Medical Hypotheses · doi:10.1016/0306-9877(94)90071-x · Cited by 253
Sleep deprivation in the rat by the disk-over-water method
Rechtschaffen, A., & Bergmann, B. M. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00020-t · Cited by 253
Zhang, Q., Wu, X., Chen, P., Liu, L., Xin, N., Tian, Y., & Dillin, A. G. (2018) · Cell · doi:10.1016/j.cell.2018.06.029 · Cited by 252
Iatsenko, I., Boquete, J., & Lemaître, B. (2018) · Immunity · doi:10.1016/j.immuni.2018.09.017 · Cited by 248
Vriend, J., & Reiter, R. J. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2014.12.013 · Cited by 246
The Continuing Puzzle of the Great Oxidation Event
Sessions, A. L., Doughty, D. M., Welander, P. V., Summons, R. E., & Newman, D. K. (2009) · Current Biology · doi:10.1016/j.cub.2009.05.054 · Cited by 244
Neuroendocrine Coordination of Mitochondrial Stress Signaling and Proteostasis
Berendzen, K. M., Durieux, J., Shao, L.-W., Tian, Y., Kim, H.-E., Wolff, S., Liu, Y., & Dillin, A. G. (2016) · Cell · doi:10.1016/j.cell.2016.08.042 · Cited by 244
NADPH oxidases and ROS signaling in the gastrointestinal tract
Aviello, G., & Knaus, U. G. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0021-8 · Cited by 235
You Are What You Host: Microbiome Modulation of the Aging Process
Heintz, C., & Mair, W. (2014) · Cell · doi:10.1016/j.cell.2014.01.025 · Cited by 222
Role of DUOX in gut inflammation: lessons from Drosophila model of gut-microbiota interactions
Kim, S., & Lee, W. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00116 · Cited by 220
Ryder, E., Blows, F., Ashburner, M., Bautista-Llácer, R., Coulson, D., Drummond, J., Webster, J., Gubb, D., Gunton, N., Johnson, G., et al. (2004) · Genetics · doi:10.1534/genetics.104.026658 · Cited by 220
Sleep deprivation induces the unfolded protein response in mouse cerebral cortex
Naidoo, N., Giang, W., Galante, R. J., & Pack, A. I. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02952.x · Cited by 219
Association of sleep disturbances with obesity, insulin resistance and the metabolic syndrome
Koren, D., & Taveras, E. M. (2018) · Metabolism · doi:10.1016/j.metabol.2018.04.001 · Cited by 216
Redox signaling mediated by the gut microbiota
Jones, R. M., & Neish, A. S. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.10.495 · Cited by 210
Sleep Deprivation and Cellular Responses to Oxidative Stress
Gopalakrishnan, A., Ji, L. L., & Cirelli, C. (2004) · SLEEP · doi:10.1093/sleep/27.1.27 · Cited by 209
A bidirectional relationship between sleep and oxidative stress in Drosophila
Hill, V. M., O'Connor, R. M., Sissoko, G. B., Irobunda, I., Leong, S., Canman, J. C., Stavropoulos, N., & Shirasu‐Hiza, M. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005206 · Cited by 200
Changes in brain gene expression after long‐term sleep deprivation
Cirelli, C., Faraguna, U., & Tononi, G. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04058.x · Cited by 197
Alzoubi, K. H., Khabour, O. F., Rashid, B. A., Damaj, M. I., & Salah, H. A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.09.017 · Cited by 194
Antioxidant defense responses to sleep loss and sleep recovery
Everson, C. A., Laatsch, C. D., & Hogg, N. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00565.2004 · Cited by 192
A protocol for in vivo detection of reactive oxygen species
Owusu-Ansah, E., Yavari, A., & Banerjee, U. K. (2008) · Protocol Exchange · doi:10.1038/nprot.2008.23 · Cited by 190
A potassium channel β-subunit couples mitochondrial electron transport to sleep
Kempf, A., Song, S. H., Talbot, C. B., & Miesenböck, G. (2019) · Nature · doi:10.1038/s41586-019-1034-5 · Cited by 190
Seugnet, L., Suzuki, Y., Vine, L., Gottschalk, L., & Shaw, P. J. (2008) · Current Biology · doi:10.1016/j.cub.2008.07.028 · Cited by 188
A Critical Period of Sleep for Development of Courtship Circuitry and Behavior in Drosophila
Kayser, M. S., Yue, Z., & Sehgal, A. (2014) · Science · doi:10.1126/science.1250553 · Cited by 187
New Drosophila transgenic reporters: insulated P-element vectors expressing fast-maturing RFP
Barolo, S., Castro, B., & Posakony, J. W. (2004) · BioTechniques · doi:10.2144/04363st03 · Cited by 187
Intestinal Stem Cell Aging: Origins and Interventions
Jasper, H. (2019) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034359 · Cited by 183
Host mitochondria influence gut microbiome diversity: A role for ROS
Yardeni, T., Tanes, C., Bittinger, K. L., Mattei, L. M., Schaefer, P. M., Singh, L. N., Wu, G. D., Murdock, D. G., & Wallace, D. C. (2019) · Science Signaling · doi:10.1126/scisignal.aaw3159 · Cited by 172
Sleep, immunity and inflammation in gastrointestinal disorders
Ali, T. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i48.9231 · Cited by 170
Sleep Deprivation in the Rat: V. Energy Use and Mediation
Bergmann, B. M., Everson, C. A., Kushida, C. A., Fang, V. S., Leitch, C. A., Schoeller, D. A., Refetoff, S., & Rechtschaffen, A. (1989) · SLEEP · doi:10.1093/sleep/12.1.31 · Cited by 166
Cellular consequences of sleep deprivation in the brain☆
Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2006.04.001 · Cited by 164
Tip-Cell Migration Controls Stalk-Cell Intercalation during Drosophila Tracheal Tube Elongation
Caussinus, E., Colombelli, J., & Affolter, M. (2008) · Current Biology · doi:10.1016/j.cub.2008.10.062 · Cited by 163
Allatostatin A Signalling in Drosophila Regulates Feeding and Sleep and Is Modulated by PDF
Chen, J., Reiher, W., Hermann-Luibl, C., Sellami, A., Cognigni, P., Kondo, S., Helfrich‐Förster, C., Veenstra, J. A., & Wegener, C. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006346 · Cited by 161
Sleep increases chromosome dynamics to enable reduction of accumulating DNA damage in single neurons
Zada, D., Bronshtein, I., Lerer‐Goldshtein, T., Garini, Y., & Appelbaum, L. (2019) · Nature Communications · doi:10.1038/s41467-019-08806-w · Cited by 161
Antidepressant effects of sleep deprivation require astrocyte-dependent adenosine mediated signaling
Hines, D. J., Schmitt, L. I., Hines, R. M., Moss, S. J., & Haydon, P. G. (2013) · Translational Psychiatry · doi:10.1038/tp.2012.136 · Cited by 160
Molecular Mechanisms of Sleep Homeostasis in Flies and MammalsPreprint
Allada, R., Cirelli, C., & Sehgal, A. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a027730 · Cited by 160
Essentials of Sleep Recordings in Drosophila: Moving Beyond Sleep Time
Andretic, R., & Shaw, P. J. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)93040-1 · Cited by 160
insomniac and Cullin-3 Regulate Sleep and Wakefulness in Drosophila
Stavropoulos, N., & Young, M. W. (2011) · Neuron · doi:10.1016/j.neuron.2011.12.003 · Cited by 159
Short duration of sleep increases risk of colorectal adenoma
Thompson, C. L., Larkin, E. K., Patel, S. R., Berger, N. A., Redline, S. S., & Li, L. (2010) · Cancer · doi:10.1002/cncr.25507 · Cited by 158
Synchronizing effects of melatonin on diurnal and circadian rhythms
Pfeffer, M., Korf, H., & Wicht, H. (2017) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.05.013 · Cited by 157
Sleep and wakefulness modulate gene expression in Drosophila
Cirelli, C., LaVaute, T. M., & Tononi, G. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03291.x · Cited by 155
Metabolism during normal, fragmented, and recovery sleep
Bonnet, M. H., Berry, R. B., & Arand, D. L. (1991) · Journal of Applied Physiology · doi:10.1152/jappl.1991.71.3.1112 · Cited by 153
Shimizu, Y., & Hendershot, L. M. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2501 · Cited by 150
Sleep deprivation induces brain region-specific decreases in glutathione levels
D’Almeida, V., Lobo, L. L., Hipólide, D. C., de Oliveira, A. C., Nóbrega, J. N., & Tufilk, S. (1998) · Neuroreport · doi:10.1097/00001756-199808240-00031 · Cited by 150
Terao, A., Steininger, T. L., Hyder, K., Apte-Deshpande, A. D., Ding, J., Rishipathak, D., Davis, R. W., Heller, H. C., & Kilduff, T. S. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00695-4 · Cited by 148
Sitaraman, D., Aso, Y., Jin, X. K., Chen, N., Felix, M., Rubin, G. M., & Nitabach, M. N. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.017 · Cited by 142
Kalyanaraman, B., Hardy, M., Podsiadły, R., Cheng, G., & Zielonka, J. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2016.08.021 · Cited by 140
Human and rat gut microbiome composition is maintained following sleep restriction
Zhang, S. L., Bai, L., Goel, N., Bailey, A., Jang, C. J., Bushman, F. D., Meerlo, P., Dinges, D. F., & Sehgal, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1620673114 · Cited by 139
Relationships between Stress Granules, Oxidative Stress, and Neurodegenerative Diseases
Chen, L., & Liu, B. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/1809592 · Cited by 139
Terao, A., Wisor, J. P., Peyron, C., Apte-Deshpande, A. D., Wurts, S. W., Edgar, D. M., & Kilduff, T. S. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.059 · Cited by 137
Cell Injury and Repair Resulting from Sleep Loss and Sleep Recovery in Laboratory Rats
Everson, C. A., Henchen, C. J., Szabo, A., & Hogg, N. (2014) · Sleep · doi:10.5665/sleep.4244 · Cited by 136
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
Ma, W., Song, J., Wang, H., Shi, F., Zhou, N., Jiang, J., Xu, Y., Zhang, L., Yang, L., & Zhou, M. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.04.006 · Cited by 134
How did life survive Earth's great oxygenation?
Fischer, W. W., Hemp, J., & Valentine, J. S. (2016) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2016.03.013 · Cited by 127
Brush border spectrin is required for early endosome recycling in Drosophila
Phillips, M. D., & Thomas, C. M. (2006) · Journal of Cell Science · doi:10.1242/jcs.02839 · Cited by 127
Role of gut microbiota in aging-related health decline: insights from invertebrate models
Clark, R. I., & Walker, D. W. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2671-1 · Cited by 121
Wang, L., Zeng, K. X., Ryoo, H. D., & Jasper, H. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004568 · Cited by 117
Stamati, K., Mudera, V., & Cheema, U. (2011) · Journal of Tissue Engineering · doi:10.1177/2041731411432365 · Cited by 115
Wu, M. N., Joiner, W. J., Dean, T., Yue, Z., Smith, C. J., Chen, D., Hoshi, T., Sehgal, A., & Koh, K. (2009) · Nature Neuroscience · doi:10.1038/nn.2454 · Cited by 114
Reactive oxygen species regulate activity-dependent neuronal plasticity in Drosophila
Oswald, M. C. W., Brooks, P. S., Zwart, M., Mukherjee, A., West, R. J. H., Giachello, C. N., Morarach, K., Baines, R., Sweeney, S. T., & Landgraf, M. (2018) · eLife · doi:10.7554/elife.39393 · Cited by 113
Pfeiffenberger, C., & Allada, R. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1003003 · Cited by 112
Wu, S.-C., Liao, C.-W., Pan, R., & Juang, J. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.03.004 · Cited by 111
Reactive Oxygen Species: Radical Factors in the Evolution of Animal Life
Taverne, Y. J. H. J., Merkus, D., Bogers, A. J. J. C., Halliwell, B. B., Duncker, D. J., & Lyons, T. W. (2018) · BioEssays · doi:10.1002/bies.201700158 · Cited by 110
No Organ Left Behind: Tales of Gut Development and Evolution
Stainier, D. Y. R. (2005) · Science · doi:10.1126/science.1108709 · Cited by 109
Shi, M., Yue, Z., Kuryatov, A., Lindstrom, J. M., & Sehgal, A. (2014) · eLife · doi:10.7554/elife.01473 · Cited by 108
Hardy, M., Zielonka, J., Karoui, H., Sikora, A., Michalski, R., Podsiadły, R., López, M., Vasquez-Vivar, J. M., Kalyanaraman, B., & Ouari, O. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7398 · Cited by 107
Pérez, E., Lindblad, J. L., & Bergmann, A. (2017) · eLife · doi:10.7554/elife.26747 · Cited by 101
Sleep, aging, and lifespan in Drosophila
Bushey, D., Hughes, K. A., Tononi, G., & Cirelli, C. (2010) · BMC Neuroscience · doi:10.1186/1471-2202-11-56 · Cited by 100
Sleep Dysfunction and Gastrointestinal Diseases.
Khanijow, V., Prakash, P., Emsellem, H. A., Borum, M. L., & Doman, D. B. (2015) · PubMed Central · Cited by 100
Bellesi, M., Bushey, D., Chini, M., Tononi, G., & Cirelli, C. (2016) · Scientific Reports · doi:10.1038/srep36804 · Cited by 99
A Role for the Molecular Chaperone Protein BiP/GRP78 in Drosophila Sleep Homeostasis
Naidoo, N. N., Casiano, V., Cater, J. R., Zimmerman, J. E., & Pack, A. I. (2007) · SLEEP · doi:10.1093/sleep/30.5.557 · Cited by 98
Xu, C., Luo, J., He, L., Montell, C., & Perrimon, N. (2017) · eLife · doi:10.7554/elife.22441 · Cited by 98
Sleep Deprivation Specifically Impairs Short-term Olfactory Memory in Drosophila
Li, X., Yu, F., & Guo, A. (2009) · SLEEP · doi:10.1093/sleep/32.11.1417 · Cited by 92
Hakim, F., Wang, Y., Carreras, A., Hirotsu, C., Zhang, J., Peris, E., & Gozal, D. (2015) · Sleep · doi:10.5665/sleep.4320 · Cited by 90
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Hulse, B. K., Haberkern, H., Franconville, R., Turner-Evans, D., Takemura, S.-Y., Wolff, T., Noorman, M., Dreher, M., Dan, C., Parekh, R., et al. (2021) · eLife · doi:10.7554/elife.66039 · Cited by 392
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Sies, H. (2021) · Redox Biology · doi:10.1016/j.redox.2021.101867 · Cited by 353
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Sang, D., Lin, K., Yang, Y., Ran, G., Li, B., Chen, C., Li, Q., Ma, Y., Lu, L., Cui, X., et al. (2023) · Cell · doi:10.1016/j.cell.2023.10.025 · Cited by 281
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Metadata
- Authors
- Vaccaro, A., Kaplan Dor, Y., Nambara, K., Pollina, E. A., Lin, C., Greenberg, M. E., & Rogulja, D.
- Affiliations
- Harvard University (US)
- Corresponding author
- Rogulja, Dragana
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2020-06
- Volume
- 181
- Issue
- 6
- Pages
- 1307-1328.e15
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W3033924751
- Cited by
- 541
- References
- 252
- Citations by year
- 2026: 79 · 2025: 127 · 2024: 109 · 2023: 92 · 2022: 63 · 2021: 53 · 2020: 18
- FWCI
- 18.77
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Pew Charitable Trusts
- New York Stem Cell Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- sleep deprivation, reactive oxygen species, oxidative stress, intestine, antioxidant enzymes, lifespan, oral antioxidants, Drosophila, mice
- MeSH terms
- Animals, Antioxidants, Drosophila, Male, Mice, Inbred CBA, Mice, Inbred C57BL, Sleep, Sleep Deprivation, Reactive Oxygen Species, Oxidative Stress, Gastrointestinal Tract, Mice
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 ›
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