IL-6 Mediated Degeneration of Forebrain GABAergic Interneurons and Cognitive Impairment in Aged Mice through Activation of Neuronal NADPH Oxidase
Open accessAbstract
BACKGROUND: Multiple studies have shown that plasma levels of the pro-inflammatory cytokine interleukin-6 (IL-6) are elevated in patients with important and prevalent adverse health conditions, including atherosclerosis, diabetes, obesity, obstructive sleep apnea, hypertension, and frailty. Higher plasma levels of IL-6, in turn, increase the risk of many conditions associated with aging including age-related cognitive decline. However, the mechanisms underlying this association between IL-6 and cognitive vulnerability remain unclear. METHODS AND FINDINGS: We investigated the role of IL-6 in brain aging in young (4 mo) and aged (24 mo) wild-type C57BL6 and genetically-matched IL-6(-/-) mice, and determined that IL-6 was necessary and sufficient for increased neuronal expression of the superoxide-producing immune enzyme, NADPH-oxidase, and this was mediated by non-canonical NFkappaB signaling. Furthermore, superoxide production by NADPH-oxidase was directly responsible for age-related loss of parvalbumin (PV)-expressing GABAergic interneurons, neurons essential for normal information processing, encoding, and retrieval in hippocampus and cortex. Targeted deletion of IL-6 or elimination of superoxide by chronic treatment with a superoxide-dismutase mimetic prevented age-related loss of PV-interneurons and reversed age-related cognitive deficits on three standard tests of spatial learning and recall. CONCLUSIONS: Present results indicate that IL-6 mediates age-related loss of critical PV-expressing GABAergic interneurons through increased neuronal NADPH-oxidase-derived superoxide production, and that rescue of these interneurons preserves cognitive performance in aging mice, suggesting that elevated peripheral IL-6 levels may be directly and mechanistically linked to long-lasting cognitive deficits in even normal older individuals. Further, because PV-interneurons are also selectively affected by commonly used anesthetic agents and drugs, our findings imply that IL-6 levels may predict adverse CNS effects in older patients exposed to these compounds through specific derangements in inhibitory interneurons, and that therapies directed at lowering IL-6 may have cognitive benefits clinically.
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
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?
IL-6 likely signals through STAT3.
“IL-6 is likely signaling through STAT3 [96].”
From Parvalbumin interneuron vulnerability and brain disorders (2021) · cites this paper as [96]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989 · see citing works
Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks
Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works
Walston, J., Hadley, E. C., Ferrucci, L., Guralnik, J. M., Newman, A. B., Studenski, S. A., Ershler, W. B., Harris, T., & Fried, L. P. (2006) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2006.00745.x · Cited by 1,605 · see citing works
Neural plasticity in the ageing brain
Burke, S. N., & Barnes, C. A. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1809 · Cited by 1,600 · see citing works
Age-Associated Increased Interleukin-6 Gene Expression, Late-Life Diseases, and Frailty
Ershler, W. B., & Keller, E. T. (2000) · Annual Review of Medicine · doi:10.1146/annurev.med.51.1.245 · Cited by 1,282 · see citing works
Daynes, R. A., Araneo, B. A., Ershler, W. B., Maloney, C., Li, G. Z., & Ryu, S. Y. (1993) · The Journal of Immunology · doi:10.4049/jimmunol.150.12.5219 · Cited by 1,264 · see citing works
Pattern Separation in the Human Hippocampal CA3 and Dentate Gyrus
Bakker, A., Kirwan, C. B., Miller, M. I., & Stark, C. E. L. (2008) · Science · doi:10.1126/science.1152882 · Cited by 1,050 · see citing works
Neurologic disease induced in transgenic mice by cerebral overexpression of interleukin 6.
Campbell, I. L., Abraham, C. R., Masliah, E., Kemper, P., Inglis, J. D., Oldstone, M. B., & Mucke, L. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.21.10061 · Cited by 1,006 · see citing works
Top-down suppression deficit underlies working memory impairment in normal aging
Gazzaley, A., Cooney, J. W., Rissman, J., & D'Esposito, M. (2005) · Nature Neuroscience · doi:10.1038/nn1543 · Cited by 934 · see citing works
Inflammatory mediators in the elderly
Krabbe, K. S., Pedersen, M., & Bruunsgaard, H. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.01.009 · Cited by 928 · see citing works
Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases
Martyn, K. D., Frederick, L. M., von Loehneysen, K., Dinauer, M. C., & Knaus, U. G. (2006) · Cellular Signalling · doi:10.1016/j.cellsig.2005.03.023 · Cited by 783 · see citing works
Apocynin Is Not an Inhibitor of Vascular NADPH Oxidases but an Antioxidant
Heumüller, S., Wind, S., Barbosa-Sicard, E., Schmidt, H. H. H. W., Busse, R., Schröder, K., & Brandes, R. P. (2008) · Hypertension · doi:10.1161/hypertensionaha.107.100214 · Cited by 735 · see citing works
Interleukin-6 in Aging and Chronic Disease: A Magnificent Pathway
Maggio, M. G., Guralnik, J. M., Longo, D. L., & Ferrucci, L. (2006) · The Journals of Gerontology Series A · doi:10.1093/gerona/61.6.575 · Cited by 687 · see citing works
Hexameric Structure and Assembly of the Interleukin-6/IL-6 α-Receptor/gp130 Complex
Boulanger, M. J., Chow, D., Brevnova, E. E., & García, K. C. (2003) · Science · doi:10.1126/science.1083901 · Cited by 647 · see citing works
NOX4 activity is determined by mRNA levels and reveals a unique pattern of ROS generation
Serrander, L., Cartier, L., Bedard, K., Banfi, B., Lardy, B., Plastre, O., Sienkiewicz, A., Fórró, L., Schlegel, W., & Krause, K.-H. (2007) · Biochemical Journal · doi:10.1042/bj20061903 · Cited by 627 · see citing works
Yang, J., Liao, X., Agarwal, M. K., Barnes, L., Auron, P. E., & Stark, G. R. (2007) · Genes & Development · doi:10.1101/gad.1553707 · Cited by 611 · see citing works
Ketamine-Induced Loss of Phenotype of Fast-Spiking Interneurons Is Mediated by NADPH-Oxidase
Behrens, M. M., Ali, S. S., Dao, D. N., Lucero, J., Shekhtman, G., Quick, K. L., & Dugan, L. L. (2007) · Science · doi:10.1126/science.1148045 · Cited by 585 · see citing works
Self-citationTrikha, M., Corringham, R. E., Klein, B., & Rossi, J. (2003) · PubMed · Cited by 506 · see citing works
Interleukin‐6: A Cytokine for Gerontolgists
Ershler, W. B. (1993) · Journal of The American Geriatrics Society · doi:10.1111/j.1532-5415.1993.tb02054.x · Cited by 480 · see citing works
Virtual navigation in humans: the impact of age, sex, and hormones on place learning.
Driscoll, I., Hamilton, D. A., Yeo, R., Brooks, W., & Sutherland, R. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2004.11.013 · Cited by 384 · see citing works
Molecular mechanisms of aging-associated inflammation.
Sarkar, D., & Fisher, P. (2006) · Cancer Letters · doi:10.1016/j.canlet.2005.04.009 · Cited by 379 · see citing works
Age differences in spatial memory in a virtual environment navigation task
Moffat, S. D., Zonderman, A. B., & Resnick, S. M. (2001) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00251-2 · Cited by 367 · see citing works
NADPH Oxidases of the Brain: Distribution, Regulation, and Function
Infanger, D. W., Sharma, R. V., & Davisson, R. L. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2006.8.1583 · Cited by 362 · see citing works
Stefanska, J., & Pawliczak, R. (2008) · Mediators of Inflammation · doi:10.1155/2008/106507 · Cited by 349 · see citing works
Neurocognitive aging: prior memories hinder new hippocampal encoding
Wilson, I. A., Gallagher, M., Eichenbaum, H., & Tanila, H. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.10.002 · Cited by 343 · see citing works
A model of hippocampal memory encoding and retrieval: GABAergic control of synaptic plasticity
Paulsen, O., & Moser, E. I. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01205-8 · Cited by 338 · see citing works
Behavioral functions of the CA3 subregion of the hippocampusPreprint
Kesner, R. P. (2007) · Learning & Memory · doi:10.1101/lm.688207 · Cited by 337 · see citing works
Kinney, J. W., Davis, C. N., Tabarean, I., Conti, B., Bartfai, T., & Behrens, M. M. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4722-05.2006 · Cited by 329 · see citing works
Self-citationWallenstein, G. V., & Hasselmo, M. E. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.1.393 · Cited by 295 · see citing works
Transthyretin protects Alzheimer's mice from the behavioral and biochemical effects of Aβ toxicity
Buxbaum, J. N., Ye, Z., Reixach, N., Friske, L., Levy, C. L., Das, P., Golde, T. E., Masliah, E., Roberts, A. R., & Bartfai, T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712197105 · Cited by 285 · see citing works
Self-citationChoi, D., Pennathur, S., Perier, C., Tieu, K., Teismann, P., Wu, D.-C., Jackson-Lewis, V. R., Vila, M., Vonsattel, J., Heinecke, J. W., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0970-05.2005 · Cited by 284 · see citing works
Sources and Targets of Reactive Oxygen Species in Synaptic Plasticity and Memory
Kishida, K. T., & Klann, E. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.233 · Cited by 264 · see citing works
The role of the dentate gyrus, CA3a,b, and CA3c for detecting spatial and environmental novelty
Hunsaker, M. R., Rosenberg, J. S., & Kesner, R. P. (2008) · Hippocampus · doi:10.1002/hipo.20464 · Cited by 252 · see citing works
Sources and Targets of Reactive Oxygen Species in Synaptic Plasticity and Memory
Kishida, K. T., & Klann, E. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.ft-8 · Cited by 245 · see citing works
Interleukin-6 Mediates the Increase in NADPH-Oxidase in the Ketamine Model of Schizophrenia
Behrens, M. M., Ali, S. S., & Dugan, L. L. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4457-08.2008 · Cited by 241 · see citing works
Self-citationCirculating interleukin‐6 mediates the febrile response to localised inflammation in rats
Cartmell, T., Poole, S., Turnbull, A. V., Rothwell, N. J., & Luheshi, G. N. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00653.x · Cited by 233 · see citing works
NADPH oxidase immunoreactivity in the mouse brain
Serrano, F., Kolluri, N., Wientjes, F. B., Card, J. P., & Klann, E. (2003) · Brain Research · doi:10.1016/s0006-8993(03)03364-x · Cited by 216 · see citing works
Molecular and cellular biology of interleukin-6 and its receptor
Keller, E. T. (1996) · Frontiers in bioscience · doi:10.2741/a136 · Cited by 185 · see citing works
A carboxyfullerene SOD mimetic improves cognition and extends the lifespan of mice
Quick, K. L., Ali, S. S., Arch, R. H., Xiong, C., Wozniak, D. F., & Dugan, L. L. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.09.014 · Cited by 184 · see citing works
Self-citationInterleukin-6 Covaries Inversely With Cognitive Performance Among Middle-Aged Community Volunteers
Marsland, A. L., Petersen, K. L., Sathanoori, R., Muldoon, M. F., Neumann, S. A., Ryan, C. M., Flory, J. D., & Manuck, S. B. (2006) · Psychosomatic Medicine · doi:10.1097/01.psy.0000238451.22174.92 · Cited by 179 · see citing works
Bermejo, P., Martín-Aragón, S., Benedí, J., Susín, C., Felici, E., Gil, P., Ribera, J. M., & Villar, Á. M. (2008) · Immunology Letters · doi:10.1016/j.imlet.2008.02.002 · Cited by 178 · see citing works
Kishida, K. T., Hoeffer, C. A., Hu, D., Pao, M., Holland, S. M., & Klann, E. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00269-06 · Cited by 159 · see citing works
Giuliani, N., Sansoni, P., Girasole, G., Vescovini, R., Passeri, G., Passeri, M., & Pedrazzoni, M. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00220-5 · Cited by 151 · see citing works
Bu, J. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00094-3 · Cited by 137 · see citing works
The role of the dorsal CA3 hippocampal subregion in spatial working memory and pattern separation
Gilbert, P. E., & Kesner, R. P. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.01.002 · Cited by 133 · see citing works
Ali, S. S., Xiong, C., Lucero, J. D., Behrens, M. M., Dugan, L. L., & Quick, K. L. (2006) · Aging Cell · doi:10.1111/j.1474-9726.2006.00252.x · Cited by 124 · see citing works
Self-citationMaki, R. A., Tyurin, V. A., Lyon, R. C., Hamilton, R. L., DeKosky, S. T., Kagan, V. E., & Reynolds, W. F. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m807731200 · Cited by 124 · see citing works
Jackman, K. A., Miller, A. A., Silva, T. M. D., Crack, P. J., Drummond, G. R., & Sobey, C. G. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2008.00073.x · Cited by 120 · see citing works
Regulation of interleukin-6 gene expression in brain of aged mice by nuclear factor κB
Ye, S.-M., & Johnson, R. W. (2001) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(01)00316-2 · Cited by 103 · see citing works
Rat hippocampal GABAergic molecular markers are differentially affected by ageing
Vela, J. M., Gutiérrez, A., Vitórica, J., & Ruano, D. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01681.x · Cited by 102 · see citing works
Preliminary Evidence for Subdimensions of Geriatric Frailty: The MacArthur Study of Successful Aging
Sarkisian, C. A., Gruenewald, T. L., Boscardin, W. J., & Seeman, T. E. (2008) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2008.02041.x · Cited by 92 · see citing works
Interleukin-6, β-amyloid peptide and NMDA interactions in rat cortical neurons
Qiu, Z., & Gruol, D. L. (2003) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(03)00158-9 · Cited by 76 · see citing works
Object recognition analysis in mice using nose-point digital video tracking
Benice, T. S., & Raber, J. (2007) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.11.002 · Cited by 74 · see citing works
Age-related deficits in mice performing working memory tasks in a water maze.
Magnusson, K. R., Scruggs, B., Aniya, J., Wright, K. C., Ontl, T., Xing, Y., & Bai, L. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.3.485 · Cited by 74 · see citing works
Luebke, J. I., & Rosene, D. L. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10668 · Cited by 60 · see citing works
Changes in the expression of the NR2B subunit during aging in macaque monkeys
Bai, L., Hof, P. R., Standaert, D. G., Xing, Y., Nelson, S. E., Young, A. B., & Magnusson, K. R. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00091-5 · Cited by 59 · see citing works
Hippocampal memory and plasticity in superoxide dismutase mutant mice
Thiels, E., & Klann, E. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00900-9 · Cited by 45 · see citing works
Neurodegeneration and peroxidases
Everse, J., & Coates, P. W. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.10.007 · Cited by 42 · see citing works
Aged APP23 mice show a delay in switching to the use of a strategy in the Barnes maze
Prut, L., Abramowski, D., Krucker, T., Levy, C. L., Roberts, A. J., Staufenbiel, M., & Wießner, C. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.017 · Cited by 38 · see citing works
Self-citationde Erausquin, G. A., Hyrc, K., Dorsey, D. A., Mamah, D. T., Dokucu, M. E., Mascó, D. H., Walton, T., Dikranian, K. T., Soriano‐Navarro, M., García‐Verdugo, J. M., et al. (2003) · Molecular Pharmacology · doi:10.1124/mol.63.4.784 · Cited by 38 · see citing works
Self-citationγ‐aminobutyric acidergic interneuron vulnerability to aging in canine prefrontal cortex
Pugliese, M., Carrasco, J. L., Geloso, M. C., Mascort, J., Michetti, F., & Mahy, N. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20223 · Cited by 36 · see citing works
Superoxide Dismutase and Hippocampal Function: Age and Isozyme Matter
Hu, D., Klann, E., & Thiels, E. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.201 · Cited by 36 · see citing works
Hunsaker, M. R., Tran, G. T., & Kesner, R. P. (2008) · Hippocampus · doi:10.1002/hipo.20429 · Cited by 35 · see citing works
Hall, D. J., Han, S.-H., & Dugan, L. L. (2009) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.808598 · Cited by 1 · see citing works
Self-citation
Flagged first, then by citations
2 of the 66 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- [32]Serrander L Cartier L Bedard K Banfi B Lardy B 2007 NOX4 activity is determined by mRNA levels and reveals a unique pattern of ROS generation. Biochem J PMC1948990 17501721
- [53]Kausler DH 1994 Learning and Memory in Normal Aging Academic Press, San Diego, CA
Cited by
Sorted by citations
Frailty and cognitive impairment—A review of the evidence and causal mechanisms
Robertson, D. A., Savva, G. M., & Kenny, R. A. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.06.004 · Cited by 759 · see citing works
Fillman, S. G., Cloonan, N., Catts, V. S., Miller, L. C., Wong, J., McCrossin, T., Cairns, M., & Weickert, C. S. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.110 · Cited by 609 · see citing works
Oxidative stress in schizophrenia: An integrated approach
Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.008 · Cited by 474 · see citing works
AMPK dysregulation promotes diabetes-related reduction of superoxide and mitochondrial function
Dugan, L. L., You, Y.-H., Ali, S. S., Diamond-Stanic, M. K., Miyamoto, S., Declèves, A., Andreyev, A. Y., Quach, T., Ly, S., Shekhtman, G., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci66218 · Cited by 456 · see citing works
Self-citationInterleukin-6, a mental cytokine
Spooren, A., Kolmus, K., Laureys, G., Clinckers, R., De Keyser, J., Haegeman, G., & Gerlo, S. (2011) · Brain Research Reviews · doi:10.1016/j.brainresrev.2011.01.002 · Cited by 352 · see citing works
Inflammation in Alzheimer’s disease: Lessons learned from microglia-depletion models
Spangenberg, E. E., & Green, K. N. (2017) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2016.07.003 · Cited by 352 · see citing works
New Insights on <i>NOX</i> Enzymes in the Central Nervous System
Nayernia, Z., Jaquet, V., & Krause, K.-H. (2014) · Antioxidants & Redox Signaling · doi:10.1089/ars.2013.5703 · Cited by 279 · see citing works
Food reward, hyperphagia, and obesity
Berthoud, H.-R., Lenard, N. R., & Shin, A. C. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00028.2011 · Cited by 275 · see citing works
Neuroinflammation and neurodegeneration in overnutrition-induced diseases
Cai, D. (2013) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2012.11.003 · Cited by 256 · see citing works
Parvalbumin interneuron vulnerability and brain disorders
Ruden, J. B., Dugan, L. L., & Konradi, C. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-020-0778-9 · Cited by 194 · see citing works
Self-citationLanz, T. A., Reinhart, V., Sheehan, M. J., Rizzo, S. J. S., Bove, S. E., James, L. C., Volfson, D., Lewis, D. A., & Kleiman, R. J. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0492-8 · Cited by 209 · see citing works
Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses
Won, H., Mah, W., & Kim, E. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00019 · Cited by 204 · see citing works
Steullet, P., Cabungcal, J.-H., Kulak, A., Kraftsik, R., Chen, Y., Dalton, T. P., Cuenod, M., & Do, K. Q. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3857-09.2010 · Cited by 202 · see citing works
Ahmad, M. H., Fatima, M., & Mondal, A. C. (2018) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2018.10.034 · Cited by 193 · see citing works
Novel Therapeutic Approaches for Alzheimer’s Disease: An Updated Review
Yu, T.-W., Lane, H., & Lin, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158208 · Cited by 182 · see citing works
Takao, K., Kobayashi, K., Hagihara, H., Ohira, K., Shoji, H., Hattori, S., Koshimizu, H., Umemori, J., Toyama, K., Nakamura, H. K., et al. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.38 · Cited by 173 · see citing works
Powell, S. B., Sejnowski, T. J., & Behrens, M. M. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.049 · Cited by 164 · see citing works
Self-citationCellular and temporal expression of NADPH oxidase (NOX) isotypes after brain injury
Cooney, S. J., Bermudez-Sabogal, S. L., & Byrnes, K. R. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-155 · Cited by 163 · see citing works
Khalifa, A. R. M., Abdel‐Rahman, E. A., Mahmoud, A. M., Ali, M. H., Noureldin, M., Saber, S. H., Mohsen, M., & Ali, S. S. (2017) · Physiological Reports · doi:10.14814/phy2.13125 · Cited by 154 · see citing works
Self-citationRengel, K. F., Pandharipande, P. P., & Hughes, C. G. (2018) · La Presse Médicale · doi:10.1016/j.lpm.2018.03.012 · Cited by 149 · see citing works
Sudduth, T. L., Powell, D. K., Smith, C. D., Greenstein, A. W., & Wilcock, D. M. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.1 · Cited by 142 · see citing works
Jung, J. E., Kim, G. S., & Chan, P. H. (2011) · Stroke · doi:10.1161/strokeaha.111.626648 · Cited by 127 · see citing works
PET Imaging of Microglial Activation—Beyond Targeting TSPO
Janssen, B., Vugts, D. J., Windhorst, A. D., & Mach, R. H. (2018) · Molecules · doi:10.3390/molecules23030607 · Cited by 127 · see citing works
Being overweight is associated with hippocampal atrophy: the PATH Through Life Study
Cherbuin, N., Sargent‐Cox, K. A., Fraser, M. A., Sachdev, P. S., & Anstey, K. J. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.106 · Cited by 119 · see citing works
Sex-related differences in oxidative stress and neurodegeneration
Tenkorang, M. A. A., Snyder, B., & Cunningham, R. L. (2017) · Steroids · doi:10.1016/j.steroids.2017.12.010 · Cited by 116 · see citing works
Factors Predisposing to Coma and Delirium
Skrobik, Y. K., Léger, C., Cossette, M., Michaud, V., & Turgeon, J. (2013) · Critical Care Medicine · doi:10.1097/ccm.0b013e318275d014 · Cited by 109 · see citing works
Hyperglycemia magnifies Schwann cell dysfunction and cell death triggered by PA-induced lipotoxicity
Padilla, A., Descorbeth, M., Almeyda, A. L., Payne, K. J., & León, M. A. D. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.013 · Cited by 107 · see citing works
Cahill‐Smith, S., & Li, J. (2014) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.12357 · Cited by 106 · see citing works
Garcia-Oscos, F., Salgado, H., Hall, S., Thomas, F., Farmer, G. E., Bermeo, J., Galindo, L. C., Ramirez, R. D., D'Mello, S., Rose-John, S., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.018 · Cited by 105 · see citing works
Redox Signaling in Neurotransmission and Cognition During Aging
Kumar, A., Yegla, B., & Foster, T. C. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7111 · Cited by 104 · see citing works
Teixeira-Santos, L., Albino‐Teixeira, A., & Pinho, D. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105280 · Cited by 103 · see citing works
NADPH oxidases: redox regulation of cell homeostasis and disease
Kračun, D., Lopes, L. R., Cifuentes-Pagano, E., & Pagano, P. J. (2025) · Physiological Reviews · doi:10.1152/physrev.00034.2023 · Cited by 104 · see citing works
Neuroinflammation in Post-Traumatic Epilepsy: Pathophysiology and Tractable Therapeutic Targets
Sharma, R., Leung, W. L., Zamani, A., O'Brien, T. J., Casillas-Espinosa, P. M., & Semple, B. D. (2019) · Brain Sciences · doi:10.3390/brainsci9110318 · Cited by 102 · see citing works
Ben‐Azu, B., Aderibigbe, A. O., Ajayi, A. M., Eneni, A.-E. O., Omogbiya, I. A., Owoeye, O., Umukoro, S., & Iwalewa, E. O. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.02.052 · Cited by 96 · see citing works
Valencia, A., Sapp, E., Kimm, J. S., McClory, H., Reeves, P., Alexander, J. S., Ansong, K. A., Masso, N., Frosch, M. P., Kegel, K. B., et al. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds516 · Cited by 93 · see citing works
RetractedBarnes, S. A., Pinto-Duarte, A., Kappe, A., Zembrzycki, A., Metzler, A., Mukamel, E. A., Lucero, J., Wang, X., Sejnowski, T. J., Markou, A., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.113 · Cited by 92 · see citing works
Self-citationThe Plasma Membrane: A Platform for Intra- and Intercellular Redox Signaling
Nordzieke, D. E., & Medraño-Fernandez, I. (2018) · Antioxidants · doi:10.3390/antiox7110168 · Cited by 90 · see citing works
Chronic Kidney Disease and Cognitive Impairment: The Kidney-Brain Axis
Xie, Z., Tong, S., Chu, X., Feng, T., & Geng, M. (2022) · Kidney Diseases · doi:10.1159/000524475 · Cited by 94 · see citing works
Mudò, G., Frinchi, M., Nuzzo, D., Scaduto, P., Plescia, F., Massenti, M. F., Carlo, M. D., Cannizzaro, C., Cassata, G., Cicero, L. L., et al. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1417-4 · Cited by 82 · see citing works
Evidence that Meningeal mast cells can worsen stroke pathology in mice.
Arac, A., Grimbaldeston, M. A., Nepomuceno, A. R. B., Olayiwola, O., Pereira, M. P., Nishiyama, Y., Tsykin, A., Goodall, G. J., Schlecht, U., Vogel, H., et al. (2014) · The American Journal of Pathology · doi:10.1016/j.ajpath.2014.06.003 · Cited by 74 · see citing works
Uric Acid Induces Cognitive Dysfunction through Hippocampal Inflammation in Rodents and Humans
Shao, X., Lu, W., Gao, F., Li, D., Hu, J., Li, Y., Zuo, Z., Jie, H., Zhao, Y., & Cen, X. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1480-16.2016 · Cited by 83 · see citing works
Senescent endothelial cells: Potential modulators of immunosenescence and ageing
Pantsulaia, I., Ciszewski, W. M., & Niewiarowska, J. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.05.011 · Cited by 80 · see citing works
Donegan, J. J., Girotti, M., Weinberg, M. S., & Morilak, D. A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3968-13.2014 · Cited by 77 · see citing works
Hou, C., Hsieh, C., Li, S., Lee, H. S., Graham, T. J. A., Xu, K., Weng, C.-C., Doot, R. K., Chu, W., Chakraborty, S. K., et al. (2017) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.7b00385 · Cited by 76 · see citing works
Self-citationNeuroinflammatory Signaling in the Pathogenesis of Alzheimer’s Disease
Uddin, M. S., Kabir, M. T., Jalouli, M., Rahman, M. A., Jeandet, P., Behl, T., Alexiou, A. T., Albadrani, G. M., Abdel‐Daim, M. M., Perveen, A., et al. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210826130210 · Cited by 76 · see citing works
Stress, sensitive periods, and substance abuse
Andersen, S. L. (2019) · Neurobiology of Stress · doi:10.1016/j.ynstr.2018.100140 · Cited by 92 · see citing works
Li, H., Ip, S., Yuan, Q., Zheng, G., Tsim, K. W. K., Dong, T. T.-X., Lin, G., Han, Y., Liu, Y., Xian, Y., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.08.194 · Cited by 70 · see citing works
Chronic intermittent cold stress sensitizes neuro-immune reactivity in the rat brain
Girotti, M., Donegan, J. J., & Morilak, D. A. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.02.008 · Cited by 71 · see citing works
Neuroinflammation, Early-Life Adversity, and Brain Development
Andersen, S. L. (2022) · Harvard Review of Psychiatry · doi:10.1097/hrp.0000000000000325 · Cited by 70 · see citing works
Athilingam, P. R., Moynihan, J. A., Chen, L., D’Aoust, R., Groer, M. E., & Kip, K. E. (2012) · Congestive Heart Failure · doi:10.1111/chf.12007 · Cited by 68 · see citing works
Ags (2015) · Journal of the American Geriatrics Society · doi:10.1111/jgs.13406 · Cited by 67 · see citing works
Guo, T., Fang, J., Tong, Z. Y., He, S., & Luo, Y. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00028 · Cited by 67 · see citing works
Molecular Mechanisms Underlying Neuroinflammation Elicited by Occupational Injuries and Toxicants
Pathak, D., & Sriram, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032272 · Cited by 69 · see citing works
Liang, G., Kow, A. S. F., Yusof, R., Tham, C. L., Ho, Y.-C., & Lee, M. T. (2024) · Biomedicines · doi:10.3390/biomedicines12010184 · Cited by 68 · see citing works
Food reward functions as affected by obesity and bariatric surgery
Shin, A. C., & Berthoud, H. R. (2011) · International Journal of Obesity · doi:10.1038/ijo.2011.147 · Cited by 64 · see citing works
Insulin dysfunction and allostatic load in bipolar disorder
Brietzke, E. M., Kapczinski, F. P., Grassi‐Oliveira, R., Grande, I., Vieta, E., & McIntyre, R. S. (2011) · Expert Review of Neurotherapeutics · doi:10.1586/ern.10.185 · Cited by 64 · see citing works
Neuroinflammatory and autonomic mechanisms in diabetes and hypertension
Han, C., Rice, M. W., & Cai, D. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00012.2016 · Cited by 63 · see citing works
The Impact of Frailty in the Elderly on the Outcome of Surgery in the Aged
Brown, N. A., & Zenilman, M. E. (2010) · Advances in Surgery · doi:10.1016/j.yasu.2010.05.014 · Cited by 60 · see citing works
Glycogen synthase kinase-3 regulates inflammatory tolerance in astrocytes
Beurel, E., & Jope, R. S. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.05.044 · Cited by 59 · see citing works
Interleukin-10 protects against aging-induced endothelial dysfunction
Kinzenbaw, D. A., Chu, Y., Silva, R. A. P., Didion, S. P., & Faraci, F. M. (2013) · Physiological Reports · doi:10.1002/phy2.149 · Cited by 58 · see citing works
Chronic stress, hippocampus and parvalbumin-positive interneurons: what do we know so far?
Zaletel, I. V., Filipović, D., & Puškaš, N. (2016) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0042 · Cited by 57 · see citing works
Hall, D. J., Han, S.-H., Chepetan, A. M., Inui, E. G., Rogers, M., & Dugan, L. L. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.119 · Cited by 56 · see citing works
Self-citationÇalışkan, G., French, T., Lacalle, S. E., del Ángel, M., Steffen, J., Heimesaat, M. M., Dunay, I. R., & Stork, O. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.10.007 · Cited by 55 · see citing works
Liu, F., Yang, L., Sun, X., Zhang, H., Pan, W. X., Wang, X., Yang, J., Ji, M., & Yuan, H. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9571-x · Cited by 54 · see citing works
Schiavone, S., Mhillaj, E., Neri, M., Morgese, M. G., Tucci, P., Bove, M., Valentino, M., Di Giovanni, G., Pomara, C., Turillazzi, E., et al. (2017) · Molecular Neurobiology · doi:10.1007/s12035-016-9791-8 · Cited by 55 · see citing works
Wang, L., Shiraki, A., Itahashi, M., Akane, H., Abe, H., Mitsumori, K., & Shibutani, M. (2013) · Toxicological Sciences · doi:10.1093/toxsci/kft183 · Cited by 52 · see citing works
Influence of glutamatergic and GABAergic neurotransmission on obstructive sleep apnea
Kaczmarski, P., Sochal, M., Strzelecki, D., Białasiewicz, P., & Gabryelska, A. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1213971 · Cited by 52 · see citing works
Wu, Y., Yao, J., & Feng, K. (2020) · Neurochemical Research · doi:10.1007/s11064-019-02931-0 · Cited by 48 · see citing works
Navigating IL-6: From molecular mechanisms to therapeutic breakthroughs
Swaroop, A. K., Negi, P., Kar, A., Mariappan, E., Natarajan, J., Namboori, P. K. K., & Selvaraj, J. (2024) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2023.12.007 · Cited by 48 · see citing works
Xu, T., Shen, X., Sun, L., Chen, Y., Zhang, B., Huang, D., & Li, W. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.4005 · Cited by 48 · see citing works
Schmalbach, B., Lepsveridze, E., Djogo, N., Papashvili, G., Kuang, F., Leshchyns’ka, I., Sytnyk, V., Nikonenko, A. G., Dityatev, A. E., Jakovčevski, I., et al. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13284 · Cited by 46 · see citing works
The specific impact of uremic toxins upon cognitive domains: a review
Franco, Á. D. O., Starosta, R. T., & Roriz‐Cruz, M. (2018) · Brazilian Journal of Nephrology · doi:10.1590/2175-8239-jbn-2018-0033 · Cited by 47 · see citing works
Jaehne, E. J., & Baune, B. T. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.12.006 · Cited by 45 · see citing works
Schiavone, S., Neri, M., Mhillaj, E., Morgese, M. G., Cantatore, S., Bové, M., Riezzo, I., Tucci, P., Pomara, C., Turillazzi, E., et al. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.76 · Cited by 45 · see citing works
Garcia-Oscos, F., Peña, D., Housini, M., Cheng, D., Lopez, D., Borland, M. S., Salgado-Delgado, R., Salgado, H., D’Mello, S., Kilgard, M. P., et al. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2014.07.020 · Cited by 43 · see citing works
Choi, D., & Lee, J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18112500 · Cited by 40 · see citing works
Thakurta, I. G., Chattopadhyay, M., Ghosh, A., & Chakrabarti, S. (2012) · Biogerontology · doi:10.1007/s10522-012-9392-5 · Cited by 39 · see citing works
Chanana, P., & Kumar, A. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00084 · Cited by 37 · see citing works
Xu, T., Sun, L., Shen, X., Chen, Y., Yin, Y., Zhang, J., Huang, D., Li, W., & Li, W. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.01.025 · Cited by 38 · see citing works
Jaehne, E. J., Corrigan, F., Toben, C. G., Jawahar, M. C., & Baune, B. T. (2015) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2015.05.021 · Cited by 38 · see citing works
Therapeutic Targeting Strategies for Early- to Late-Staged Alzheimer’s Disease
Kang, Y. J., Diep, Y. N., Tran, M., & Cho, H. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249591 · Cited by 36 · see citing works
Abdel‐Rahman, E. A., Mahmoud, A. M., Khalifa, A. M., & Ali, S. S. (2016) · The Journal of Physiology · doi:10.1113/jp271471 · Cited by 35 · see citing works
Self-citationInitial evidence linking synaptic superoxide production with poor short-term memory in aged mice
Ali, S. S., Young, J. W., Wallace, C. K., Gresack, J. E., Jeste, D. V., Geyer, M. A., Dugan, L. L., & Risbrough, V. B. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.009 · Cited by 32 · see citing works
Self-citationWoodie, L. N., Johnson, R. M., Ahmed, B., Fowler, S., Haynes, W., Carmona, B. A., Reed, M. N., Suppiramaniam, V. D., & Greene, M. W. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.05.053 · Cited by 31 · see citing works
Jaiswal, G., & Kumar, P. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113699 · Cited by 31 · see citing works
Early Adolescent Emergence of Reversal Learning Impairments in Isolation-Reared Rats
Powell, S. B., Khan, A., Young, J. W., Scott, C. N., Buell, M. R., Caldwell, S., Tsan, E., de Jong, L. A. W., Acheson, D. T., Lucero, J. D., et al. (2015) · Developmental Neuroscience · doi:10.1159/000430091 · Cited by 30 · see citing works
Self-citationKikuchihara, Y., Abe, H., Tanaka, T., Kato, M., Wang, L., Ikarashi, Y., Yoshida, T., & Shibutani, M. (2015) · Toxicology · doi:10.1016/j.tox.2015.02.005 · Cited by 29 · see citing works
Toxoplasma gondii infection and schizophrenia: an inter-kingdom communication perspective
Elsheikha, H., & Zhu, X.-Q. (2016) · Current Opinion in Infectious Diseases · doi:10.1097/qco.0000000000000265 · Cited by 29 · see citing works
Amraie, E., Pouraboli, I., & Rajaei, Z. (2020) · Food & Function · doi:10.1039/d0fo01030h · Cited by 29 · see citing works
Potter, H. G., Kowash, H. M., Woods, R. M., Revill, G., Grime, A., Deeney, B., Burgess, M. A., Aarons, T., Glazier, J. D., Neill, J. C., et al. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.12.003 · Cited by 29 · see citing works
Lonnemann, N., Hosseini, S., Ohm, M., Geffers, R., Hiller, K., Dinarello, C. A., & Körte, M. (2022) · eLife · doi:10.7554/elife.75889 · Cited by 28 · see citing works
Gut microbiota, pathogenic proteins and neurodegenerative diseases
Wei, W., Wang, S., Xu, C., Zhou, X., Lian, X., He, L., & Li, K. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.959856 · Cited by 29 · see citing works
Алекcеенко, А. В., Lemeshchenko, V. V., Pekun, T. G., Waseem, T. V., & Fedorovich, S. V. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.02.051 · Cited by 28 · see citing works
Andy, S. N., Pandy, V., Alias, Z., & Kadir, H. A. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.05.035 · Cited by 27 · see citing works
Sun, Z., Li, X., Liu, Y., Dong, X., Han, Y., Li, Y., Luo, J., & Li, W. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02717-y · Cited by 27 · see citing works
Rengasamy, M. L., Marsland, A. L., Spada, M. L., Hsiung, K. S., Kovats, T., & Price, R. B. (2021) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2021.100177 · Cited by 26 · see citing works
Atzori, M., García‐Oscos, F., & Méndez, J. A. T. (2012) · Future Medicinal Chemistry · doi:10.4155/fmc.12.156 · Cited by 25 · see citing works
Ben‐Azu, B., Adebayo, O. G., Fokoua, A. R., Onuelu, J. E., Asiwe, J. N., Moke, E. G., Omogbiya, I. A., Okpara, O. L., Okoro, J. E., Oghenevwerutevwe, O. M., et al. (2024) · Brain Disorders · doi:10.1016/j.dscb.2024.100122 · Cited by 23 · see citing works
Khan, A., de Jong, L. A. W., Kamenski, M. E., Higa, K. K., Lucero, J. D., Young, J. W., Behrens, M. M., & Powell, S. B. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.022 · Cited by 19 · see citing works
Self-citationPlaza-Briceño, W., Estay, S. F., de la Fuente-Ortega, E., Gutiérrez, C., Sánchez, G., Hidalgo, C., Chávez, A. E., & Haeger, P. A. (2019) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7787 · Cited by 18 · see citing works
- Authors
- Dugan, L. L., Ali, S. S., Shekhtman, G., Roberts, A. J., Lucero, J., Quick, K. L., & Behrens, M. M.
- Affiliations
- University of California San Diego (US)
- Scripps Research Institute (US)
- Corresponding author
- Dugan, Laura L.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2009-05-13
- Volume
- 4
- Issue
- 5
- Pages
- e5518
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC2678193
- OpenAlex
- W2000833088
- Cited by
- 165
- References
- 66
- Citations by year
- 2026: 4 · 2025: 8 · 2024: 9 · 2023: 10 · 2022: 9 · 2021: 12 · 2020: 9 · 2019: 11 · 2018: 10 · 2017: 10 · 2016: 12 · 2015: 11 · 2014: 11 · 2013: 13 · 2012: 7
- FWCI
- 5.52
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Larry L. Hillblom Foundation
- National Institutes of Health (NS057096)
- National Institute on Aging (K25AG026379, R21AG030320, AG030320)
- National Institute of Neurological Disorders and Stroke (P30NS057096, NS057096)
- Topics
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Antioxidants, Aging, Portulaca oleracea
- Keywords
- interleukin-6, brain aging, GABAergic interneurons, parvalbumin interneurons, NADPH oxidase, superoxide, non-canonical NF-κB signaling, age-related cognitive decline, neuroinflammation, superoxide dismutase mimetic, spatial learning and memory
- MeSH terms
- NADPH Oxidase 2, Aging, Animals, Cell Nucleus, Cognition, gamma-Aminobutyric Acid, Interneurons, Membrane Glycoproteins, Mice, Transgenic, Nerve Degeneration, Neurons, Parvalbumins, Superoxide Dismutase, Synaptosomes, Interleukin-6, Prosencephalon, NADPH Oxidases, 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 ›
Are you an author, or do you see a problem with this page? Request a review