The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Glutamine synthetase down-regulation reduces astrocyte protection against glutamate excitotoxicity to neurons
Open accessAbstract
Although the role of astrocyte glutamate transporters in glutamate clearance is well illustrated, the role of glutamine synthetase (GS) that influences this process remains to be elucidated. We examined whether GS affected the uptake of glutamate in astrocytes in vitro. The glutamate uptake was assessed by measuring the concentration of glutamate and glutamine in culture medium in the presence or absence of glutamate. We demonstrated that inhibition of GS in astrocytes by MSO significantly impaired glutamate uptake and glutamine release. Conversely, induction of GS expression in astrocytes by gene transfer significantly enhanced the glutamate uptake and glutamine release. When an inflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) was applied to the cultures, it significantly reduced GS expression and inhibited glutamate-induced GS activation resulting in increased excitotoxicity to neurons. These results suggest that GS in astrocytes may represent a novel target for neuroprotection against neuronal dysfunction and death that occur in many neurological disorders.
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 doesn’t support the claim as written.
In the citing paper
“When a large amount of glutamate is released from neuronal vesicles, glutamate clearance is mainly achieved by glutamate transporters (EAATs) on the membrane of astrocytes, which transport excess glutamate into astrocytes, where it is converted to glutamylamine through the action of glutamine synthase, reducing damage to neurons. 88 , 89”
From Major depressive disorder: hypothesis, mechanism, prevention and treatment (2024) · cites this paper as [89]
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
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
Microglia: a sensor for pathological events in the CNS
Kreutzberg, G. W. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)10049-7 · Cited by 4,396
Kamata, H., Honda, S.-I., Maeda, S., Chang, L., Hirata, H., & Karin, M. (2005) · Cell · doi:10.1016/j.cell.2004.12.041 · Cited by 1,792
Microglia and inflammation-mediated neurodegeneration: Multiple triggers with a common mechanism
Block, M. L., & Hong, J.-S. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.06.004 · Cited by 1,557
Glutamate neurotoxicity in cortical cell culture
Choi, D. W., Maulucci-Gedde, M., & Kriegstein, A. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-02-00357.1987 · Cited by 1,506
Okada, S., Nakamura, M., Katoh, H., Miyao, T., Shimazaki, T., Ishii, K., Yamane, J., Yoshimura, A., Iwamoto, Y., Toyama, Y., et al. (2006) · Nature Medicine · doi:10.1038/nm1425 · Cited by 991
Oliver, C., Starke-Reed, P. E., Stadtman, E. R., Liu, G. J., Carney, J. M., & Floyd, R. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.13.5144 · Cited by 771
Astrocytic control of glutamatergic activity: astrocytes as stars of the show.
Hertz, L., & Zielke, H. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.10.008 · Cited by 490
Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity
Shin, J., Fang, Z.-H., Yu, Z.-X., Wang, C.-E., Li, S., & Li, X. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200508072 · Cited by 488
Werner, P., Pitt, D., & Raine, C. S. (2001) · Annals of Neurology · doi:10.1002/ana.1077 · Cited by 488
Inflammatory processes in amyotrophic lateral sclerosis
McGeer, P. L., & McGeer, E. G. (2002) · Muscle & Nerve · doi:10.1002/mus.10191 · Cited by 470
Cited by
Sorted by citations
Berk, M., Kapczinski, F., Andreazza, A. C., Dean, O. M., Giorlando, F., Maes, M., Yücel, M., Gama, C. S., Dodd, S., Dean, B., et al. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.10.001 · Cited by 1,178
Major depressive disorder: hypothesis, mechanism, prevention and treatment
Cui, L., Li, S., Wang, S., Wu, X., Liu, Y., Yu, W., Wang, Y., Tang, Y., Xia, M., & Li, B. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01738-y · Cited by 1,244
“88,89 In the classic glutamate-glutamine cycle, astrocytes and neurons convert glutamate to the nonexcitatory amino acid glutamine, which is then released back into the extracellular space and absorbed by neurons.”
BackgroundSelf-citationManganese Is Essential for Neuronal Health
Horning, K. J., Caito, S. W., Tipps, K. G., Bowman, A. B., & Aschner, M. (2015) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071714-034419 · Cited by 623
Activation of microglia and astrocytes: a roadway to neuroinflammation and Alzheimer’s disease
Kaur, D., Sharma, V., & Deshmukh, R. R. (2019) · Inflammopharmacology · doi:10.1007/s10787-019-00580-x · Cited by 503
Astrocytes: Role and Functions in Brain Pathologies
Siracusa, R., Fusco, R., & Cuzzocrea, S. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01114 · Cited by 361
Andersen, J. V., Schousboe, A., & Verkhratsky, A. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102331 · Cited by 263
Astrocyte dysfunction in Alzheimer disease
Acosta, C., Anderson, H. D., & Anderson, C. M. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24075 · Cited by 262
The Role of Astrocytes in Neuroprotection after Brain Stroke: Potential in Cell Therapy
Becerra-Calixto, A., & Cardona‐Gómez, G. P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00088 · Cited by 239
APOE ε4/ε4 diminishes neurotrophic function of human iPSC-derived astrocytes
Zhao, J., Davis, M. D., Martens, Y. A., Shinohara, M., Graff-Radford, N. R., Younkin, S. G., Wszolek, Z. K., Kanekiyo, T., & Bu, G. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx155 · Cited by 221
Dual roles of astrocytes in plasticity and reconstruction after traumatic brain injury
Zhou, Y., Shao, A., Yao, Y., Tu, S., Deng, Y., & Zhang, J. (2020) · Cell Communication and Signaling · doi:10.1186/s12964-020-00549-2 · Cited by 211
Astrocytic-neuronal crosstalk: Implications for neuroprotection from brain injury
Barreto, G. E., González, J., Torres, Y. P., & Morales, L. (2011) · Neuroscience Research · doi:10.1016/j.neures.2011.06.004 · Cited by 194
Can satellite glial cells be therapeutic targets for pain control?
Jasmin, L., Vit, J., Bhargava, A., & Ohara, P. T. (2010) · Neuron Glia Biology · doi:10.1017/s1740925x10000098 · Cited by 176
Mechanisms of Endogenous Neuroprotective Effects of Astrocytes in Brain Injury
Bylicky, M. A., Mueller, G. P., & Day, R. M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6501031 · Cited by 170
Andersen, J. V., & Schousboe, A. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15811 · Cited by 161
Astrocytes as Guardians of Neuronal Excitability: Mechanisms Underlying Epileptogenesis
Verhoog, Q. P., Holtman, L., Aronica, E., & van Vliet, E. A. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.591690 · Cited by 149
The Glutamate/ GABA ‐Glutamine Cycle: Insights, Updates, and Advances
Andersen, J. V. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70029 · Cited by 170
Reactive astrocytes give neurons less support: implications for Alzheimer's disease
Steele, M. L., & Robinson, S. R. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.09.018 · Cited by 145
Encephalitic Arboviruses: Emergence, Clinical Presentation, and Neuropathogenesis
Salimi, H., Cain, M. D., & Klein, R. S. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0443-5 · Cited by 135
Villapol, S., Byrnes, K. R., & Symes, A. J. (2014) · Frontiers in Neurology · doi:10.3389/fneur.2014.00082 · Cited by 128
Diversity of astroglial responses across human neurodegenerative disorders and brain aging
Ferrer, I. (2017) · Brain Pathology · doi:10.1111/bpa.12538 · Cited by 135
Song, X., Gong, Z., Liu, K., Kou, J., Liu, B., & Liu, K. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101559 · Cited by 113
Avila-Muñoz, E., & Arias, C. (2014) · Ageing Research Reviews · doi:10.1016/j.arr.2014.07.004 · Cited by 114
Alzheimer’s Disease: Mechanism and Approach to Cell Therapy
Amemori, T., Jendelová, P., Růžička, J., Urdzíková, L. M., & Syková, E. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161125961 · Cited by 110
Glutamine Acts as a Neuroprotectant against DNA Damage, Beta-Amyloid and H2O2-Induced Stress
Chen, J., & Herrup, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033177 · Cited by 97
Glutamine deficiency in the prefrontal cortex increases depressive-like behaviours in male mice
Lee, Y., Son, H., Kim, G., Kim, S., Lee, D. H., Roh, G. S., Kang, S. S., Cho, G. J., Choi, W. S., & Kim, H. J. (2013) · Journal of Psychiatry & Neuroscience · doi:10.1503/jpn.120024 · Cited by 94
Rege, S., & Hodgkinson, S. J. (2013) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867413499077 · Cited by 90
Silvestrin, R. B., Bambini-Júnior, V., Galland, F., Bobermin, L. D., Quincozes‐Santos, A., Abib, R. T., Zanotto, C., Batassini, C., Brolese, G., Gonçalves, C., et al. (2012) · Brain Research · doi:10.1016/j.brainres.2012.11.048 · Cited by 99
Glial Glutamine Homeostasis in Health and Disease
Andersen, J. V., & Schousboe, A. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03771-1 · Cited by 92
Glutamate transporters in brain ischemia: to modulate or not?
Krzyżanowska, W., Pomierny, B., Filip, M., & Pera, J. (2014) · Acta Pharmacologica Sinica · doi:10.1038/aps.2014.1 · Cited by 86
Narne, P., Pandey, V., & Phanithi, P. B. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.05.008 · Cited by 84
Metabotropic glutamatergic receptors and their ligands in drug addiction
Pomierny-Chamioło, L., Rup, K., Pomierny, B., Niedzielska, E., Kalivas, P. W., & Filip, M. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.12.012 · Cited by 84
Dimethyl Fumarate Modulation of Immune and Antioxidant Responses: Application to HIV Therapy
Gill, A. J., & Kolson, D. L. (2013) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.2013007247 · Cited by 81
Yamamoto, N., Fujii, Y., Kasahara, R., Tanida, M., Ohora, K., Ono, Y., Suzuki, K., & Sobue, K. (2016) · Glia · doi:10.1002/glia.22974 · Cited by 80
Glutamate metabolism and HIV-associated neurocognitive disorders
Vázquez-Santiago, F. J., Noel, R. J., Porter, J. T., & Rivera‐Amill, V. (2014) · Journal of NeuroVirology · doi:10.1007/s13365-014-0258-2 · Cited by 79
Protection by Neuroglobin Expression in Brain Pathologies
Báez, E., Echeverría, V., Cabezas, R., Avila-Rodriguez, M. F., Garcia-Segura, L., & Barreto, G. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00146 · Cited by 70
Norden, D. M., Trojanowski, P. J., Walker, F. R., & Godbout, J. P. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.04.014 · Cited by 73
Brison, É., Jacomy, H., Desforges, M., & Talbot, P. J. (2013) · Journal of Virology · doi:10.1128/jvi.02972-13 · Cited by 71
Quincozes‐Santos, A., Bobermin, L. D., de Assis, A. M., Gonçalves, C., & Souza, D. O. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.09.013 · Cited by 70
Insect models of central nervous system energy metabolism and its links to behavior
Rittschof, C. C., & Schirmeier, S. (2017) · Glia · doi:10.1002/glia.23235 · Cited by 71
Li, Z., Liu, Q., Liu, C., Li, C., Li, Y., Li, S., Liu, X., & Shao, J. (2016) · Toxicology in Vitro · doi:10.1016/j.tiv.2016.11.002 · Cited by 65
Astrocyte and glutamate involvement in the pathogenesis of epilepsy in Alzheimer's disease
Dejakaisaya, H., Kwan, P., & Jones, N. C. (2021) · Epilepsia · doi:10.1111/epi.16918 · Cited by 64
Proteomic differences in the hippocampus and cortex of epilepsy brain tissue
Pires, G., Leitner, D., Drummond, E., Kanshin, E., Nayak, S., Askenazi, M., Faustin, A., Friedman, D. J., Debure, L., Ueberheide, B. M., et al. (2021) · Brain Communications · doi:10.1093/braincomms/fcab021 · Cited by 67
Barreto, G. E., White, R., Xu, L., Palm, C. J., & Giffard, R. G. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.08.015 · Cited by 61
Chakraborty, P., Dey, A., Gopalakrishnan, A. V., Swati, K., Ojha, S. K., Prakash, A., Kumar, D., Ambasta, R. K., Jha, N. K., Jha, S. K., et al. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101838 · Cited by 59
Prevention of Cognitive Decline in Alzheimer’s Disease by Novel Antioxidative Supplements
Tadokoro, K., Ohta, Y., Inufusa, H., Loon, A. F. N., & Abe, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061974 · Cited by 58
Mehla, R., Bivalkar-Mehla, S., Nagarkatti, M., & Chauhan, A. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-239 · Cited by 55
Brain edema in acute liver failure and chronic liver disease: Similarities and differences
Bosoi, C. R., & Rose, C. F. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.01.015 · Cited by 54
Biomaterials to Neuroprotect the Stroke Brain: A Large Opportunity for Narrow Time Windows
González‐Nieto, D., Fernández-Serra, R., Pérez‐Rigueiro, J., Panetsos, F., Martínez‐Murillo, R., & Guinea, G. V. (2020) · Cells · doi:10.3390/cells9051074 · Cited by 54
houcke, J. V., Mariën, V., Zandecki, C., Vanhunsel, S., Moons, L., Ayana, R., Seuntjens, E., & Arckens, L. (2021) · Aging Cell · doi:10.1111/acel.13464 · Cited by 51
Kostić, M. S., Živković, N., Cvetanović, A., Stojanović, I. R., & Čolić, M. J. (2016) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2016.11.006 · Cited by 50
Vandresen-Filho, S., Martins, W. C., Bertoldo, D. B., Mancini, G., Herculano, B., Bem, A. F. D., & Tasca, C. I. (2013) · Neurochemistry International · doi:10.1016/j.neuint.2013.03.002 · Cited by 51
Astrocytes as a target for neuroprotection: Modulation by progesterone and dehydroepiandrosterone
Arbo, B. D., Benetti, F., & Ribeiro, M. F. M. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.03.010 · Cited by 52
Lau, C. L., Perreau, V. M., Chen, M. J., Cate, H. S., Merlo, D., Cheung, N. S., O'Shea, R. D., & Beart, P. M. (2012) · Journal of Cellular Physiology · doi:10.1002/jcp.22838 · Cited by 49
Oklinski, M. K., Skowronski, M. T., Skowrońska, A., Rützler, M. R., Nørgaard, K., Nieland, J. D., Kwon, T., & Nielsen, S. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17122050 · Cited by 49
Targeting inflammation as a therapeutic strategy for drug-resistant epilepsies
Vitaliti, G., Pavone, P., Mahmood, F., Nunnari, G., & Falsaperla, R. (2014) · Human Vaccines & Immunotherapeutics · doi:10.4161/hv.28400 · Cited by 48
Protective Effects of Gastrodin Against Autophagy‐Mediated Astrocyte Death
Wang, X., Tian, Z., Zhang, N., Han, J., Guo, H., Zhao, M., & Liu, S. (2015) · Phytotherapy Research · doi:10.1002/ptr.5538 · Cited by 48
Mshaty, A., Haijima, A., Takatsuru, Y., Ninomiya, A., Yajima, H., Kokubo, M., Khairinisa, M. A., Miyazaki, W., Amano, I., & Koibuchi, N. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111710 · Cited by 50
Gottipati, M. K., Kalinina, I. V., Bekyarova, E. B., Haddon, R. C., & Parpura, V. (2012) · Nano Letters · doi:10.1021/nl302178s · Cited by 42
Wang, Y., Sun, M., Hou, Q., & Parpura, V. (2013) · Glia · doi:10.1002/glia.22453 · Cited by 42
Self-citationBellaver, B., Bobermin, L. D., de Souza, D. G., Rodrigues, M. D. N., de Assis, A. M., Wajner, M., Gonçalves, C., Souza, D. O., & Quincozes‐Santos, A. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.06.018 · Cited by 42
Neuroimmune System as a Driving Force for Plasticity Following CNS Injury
O’Reilly, M. L., & Tom, V. J. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00187 · Cited by 44
Fomin, V., Richard, P., Hoque, M., Li, C., Gu, Z., Fissore-O'Leary, M., Tian, B., Prives, C. L., & Manley, J. L. (2018) · Molecular and Cellular Biology · doi:10.1128/mcb.00155-18 · Cited by 44
Repeated Mesenchymal Stromal Cell Treatment Sustainably Alleviates Machado-Joseph Disease
Miranda, C. O., Marcelo, A., Silva, T. P., Barata, J., Vasconcelos‐Ferreira, A., Pereira, D., Nóbrega, C., Duarte, S., Barros, I., Alves, J., et al. (2018) · Molecular Therapy · doi:10.1016/j.ymthe.2018.07.007 · Cited by 37
Yu, N., Liu, H., & Di, Q. (2013) · Current Neuropharmacology · doi:10.2174/157015913804999540 · Cited by 38
Lv, J., Ma, S., Zhang, X., Zheng, L., Ma, Y., Zhao, X., Lai, W., Shen, H., Wang, Q., & Ji, J. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.07.028 · Cited by 38
Zhou, Y., Chen, Q., Wang, Y., Wu, H., Xu, W., Pan, Y., Gao, S., Dong, X., Zhang, J. H., & Shao, A. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00581 · Cited by 36
Self-citationSchmitz, F., Pierozan, P., Rodrigues, A. F., Biasibetti, H., Grings, M., Zanotto, B., Coelho, D. M., Vargas, C. R., Leipnitz, G., & Wyse, A. T. S. (2017) · Molecular Neurobiology · doi:10.1007/s12035-016-0289-1 · Cited by 35
Kalecký, K., & Bottiglieri, T. (2023) · npj Parkinson's Disease · doi:10.1038/s41531-023-00531-y · Cited by 32
Age-Dependent Astroglial Vulnerability to Hypoxia and Glutamate: The Role for Erythropoietin
Lourhmati, A., Buniatian, G. H., Paul, C., Verleysdonk, S., Bücheler, R., Buadze, M., Proksch, B., Schwab, M. G., Gleiter, C. H., & Danielyan, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077182 · Cited by 33
Roles of Specialized Pro-Resolving Lipid Mediators in Cerebral Ischemia Reperfusion Injury
Yin, P., Wei, Y., Wang, X., Zhu, M., & Feng, J. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00617 · Cited by 34
Kitaoka, Y., Munemasa, Y., Hayashi, Y., Kuribayashi, J., Koseki, N., Kojima, K., Kumai, T., & Ueno, S. (2011) · Endocrinology · doi:10.1210/en.2011-0046 · Cited by 30
Alzheimer’s Disease, Astrocytes and Kynurenines
Dézsi, L., Tuka, B., Martos, D., & Vécsei, L. (2015) · Current Alzheimer Research · doi:10.2174/156720501205150526114000 · Cited by 33
Hoshi, A., Yamamoto, T., Shimizu, K., Sugiura, Y., & Ugawa, Y. (2010) · Experimental Neurology · doi:10.1016/j.expneurol.2010.09.016 · Cited by 31
王学文, Kang, J., Li, X., Wu, P., Huang, Y., Huang, Y., Feng, J., & Feng, J. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.118016 · Cited by 30
Jeitner, T. M., & Cooper, A. J. L. (2013) · Metabolic Brain Disease · doi:10.1007/s11011-013-9439-6 · Cited by 30
Cao, P., Zhang, J., Huang, Y., Fang, Y., Lyu, J., & Shen, Y. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2018.12.018 · Cited by 29
Mannelli, L. D. C., Tenci, B., Zanardelli, M., Failli, P., & Ghelardini, C. (2015) · Neural Plasticity · doi:10.1155/2015/396908 · Cited by 29
Ammonia impairs glutamatergic communication in astroglial cells: protective role of resveratrol
Bobermin, L. D., Hansel, G., Scherer, E. B. S., Wyse, Â. T. D. S., Souza, D. O., Quincozes‐Santos, A., & Gonçalves, C. (2015) · Toxicology in Vitro · doi:10.1016/j.tiv.2015.08.008 · Cited by 29
Astrocyte glutamate transporters are increased in an early sporadic model of synucleinopathy
Diniz, L. P., Araújo, A. P. B., Matias, I. C. P., Garcia, M. N., Barros‐Aragão, F. G. Q., Reis, R. A. D. M., Foguel, D., Braga, C. A. C. A., Figueiredo, C. P., Romão, L. F., et al. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104758 · Cited by 27
Gruol, D. L., Vo, K., & Bray, J. G. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00234 · Cited by 29
Cross-Talk Between Neurons and Astrocytes in Response to Bilirubin: Early Beneficial Effects
Falcão, A. S., Silva, R. F. M., Vaz, A. R., Silva, S. L., Fernandes, A. M. A., & Brites, D. M. T. O. (2013) · Neurochemical Research · doi:10.1007/s11064-012-0963-2 · Cited by 28
Proteomics Reveals Profound Metabolic Changes in the Alcohol Use Disorder Brain
Enculescu, C., Kerr, E. D., Yeo, K. Y. B., Dodd, P. R., Schenk, G., Fortes, M. R. S., & Schulz, B. L. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.8b00660 · Cited by 30
Down-regulation of glutamine synthetase enhances migration of rat astrocytes after in vitro injury
Zou, J., Wang, Y., Mu, H., Xiang, J., Wu, W., Zhang, B., & Xie, P. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.12.018 · Cited by 27
Self-citationTerrasso, A. P., Pinto, C., Serra, M., Filipe, A., Almeida, S., Ferreira, A. L. A., Pedroso, P., Brito, C., & Alves, P. M. (2015) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2014.12.011 · Cited by 27
Inflammation as a Mechanism of Bipolar Disorder Neuroprogression
Barichello, T., Giridharan, V. V., Bhatti, G. S., Sayana, P., Doifode, T., Macêdo, D. S., & Quevedo, J. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_173 · Cited by 28
Bradesi, S., Golovatscka, V., Ennes, H. S., McRoberts, J. A., Karagiannidis, I., Bakirtzi, K., Pothoulakis, C., & Mayer, E. A. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00182.2011 · Cited by 27
Kalkman, H. O. (2019) · Pharmaceuticals · doi:10.3390/ph12030113 · Cited by 32
The cGAS−STING-mediated ROS and ferroptosis are involved in manganese neurotoxicity
Zhang, Z., Yang, J., Zhou, Q., Zhong, S., Liu, J., Zhang, X., Chang, X., & Wang, H. (2024) · Journal of Environmental Sciences · doi:10.1016/j.jes.2024.05.003 · Cited by 27
Host response to intravenous injection of epsilon toxin in mouse model: A proteomic view
Kumar, B., Alam, S. I., & Kumar, O. (2012) · PROTEOMICS · doi:10.1002/pmic.201200227 · Cited by 26
Manganese Provision in Parenteral Nutrition: An Update
Livingstone, C. (2017) · Nutrition in Clinical Practice · doi:10.1177/0884533617702837 · Cited by 26
Cortical spreading depression-induced preconditioning in the brain
Cui, L., Feng, J., Shen, P.-P., Hou, S., Ma, D., Zhao, M.-M., Zhu, M., Zhang, J., & Feng, L. (2016) · Neural Regeneration Research · doi:10.4103/1673-5374.194759 · Cited by 24
Raphael, I., Gomez‐Rivera, F., Raphael, R. A., Robinson, R. R., Nalawade, S. A., & Forsthuber, T. G. (2019) · JCI Insight · doi:10.1172/jci.insight.132527 · Cited by 24
Singh, K., Trivedi, R., Verma, A. M., D'Souza, M. M., Koundal, S., Rana, P., Baishya, B., & Khushu, S. (2017) · NMR in Biomedicine · doi:10.1002/nbm.3764 · Cited by 23
Neurotoxic potential of reactive astrocytes in canine distemper demyelinating leukoencephalitis
Klemens, J., Ciurkiewicz, M., Chludzinski, E., Iseringhausen, M., Klotz, D., Pfankuche, V., Ulrich, R., Herder, V., Puff, C., Baumgärtner, W., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-48146-9 · Cited by 24
Lin, C.-H., Chen, H.-Y., & Wei, K. (2020) · Cells · doi:10.3390/cells9122585 · Cited by 23
Comparative proteomic analysis of Bactrocera dorsalis (Hendel) in response to thermal stress
Wei, D., Jia, F., Tian, C.-B., Tian, Y., Smagghe, G. J., Dou, W., & Wang, J. (2015) · Journal of Insect Physiology · doi:10.1016/j.jinsphys.2015.01.012 · Cited by 23
Zhu, Z., Wang, Y., Wang, Y., Fu, M., Luo, X., Wang, G., Zhang, J., Yang, X., Shan, W., Li, C., et al. (2024) · Environmental Pollution · doi:10.1016/j.envpol.2024.124798 · Cited by 22
Self-citationRole of Astrocytes in Neurodegenerative Diseases
George, E., González, J., Capani, F., & Morales, L. (2011) · InTech eBooks · doi:10.5772/31166 · Cited by 21
Gottipati, M. K., Bekyarova, E. B., Haddon, R. C., & Parpura, V. (2015) · Amino Acids · doi:10.1007/s00726-015-1970-9 · Cited by 21
Why are neurotransmitters neurotoxic? An evolutionary perspective
Harris, K. D., Weiss, M., & Zahavi, A. A. (2014) · F1000Research · doi:10.12688/f1000research.4828.2 · Cited by 24
Metadata
- Authors
- Zou, J., Wang, Y.-X., Dou, F.-F., Lü, H.-Z., Ma, Z.-W., Lu, P.-H., & Xu, X.-M.
- Affiliations
- Shanghai Jiao Tong University (CN)
- Corresponding author
- Lu, Pei-Hua
- Xu, Xiao-Ming
- Venue
- Neurochemistry International
- Publisher
- Elsevier BV
- Published
- 2010-03
- Volume
- 56
- Issue
- 4
- Pages
- 577-584
- ISSN
- 0197-0186 (ISSN-L)
- PMC
- PMC2831119
- OpenAlex
- W2070004275
- Cited by
- 181
- References
- 47
- Citations by year
- 2026: 10 · 2025: 8 · 2024: 8 · 2023: 10 · 2022: 8 · 2021: 10 · 2020: 16 · 2019: 10 · 2018: 9 · 2017: 11 · 2016: 16 · 2015: 14 · 2014: 12 · 2013: 16 · 2012: 9
- FWCI
- 5.04
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Neurochemistry International (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Funders
- National Institutes of Health (7r01ns050243-06)
- National Institute of Neurological Disorders and Stroke (R01NS111776, NS52290, R01NS059622, R01NS052290, R01-NS050243, R01NS036350, NS36350, NS50243)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- glutamine synthetase, astrocytes, glutamate excitotoxicity, glutamate uptake, glutamine release, glutamate transporters, glutamate clearance, TNF-α, neuroprotection, gene transfer, neuronal cell death
- MeSH terms
- Animals, Astrocytes, Cell Survival, Cells, Cultured, Glutamate-Ammonia Ligase, Nerve Degeneration, Neurons, Plasmids, Transfection, Tumor Necrosis Factor-alpha, Blotting, Western, Down-Regulation, Rats, Sprague-Dawley, Apoptosis, Glutamic Acid, Excitatory Amino Acids, 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