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N-Acetylcysteine Normalizes Neurochemical Changes in the Glutathione-Deficient Schizophrenia Mouse Model During Development
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Background Glutathione (GSH) is the major cellular redox-regulator and antioxidant. Redox-imbalance due to genetically impaired GSH synthesis is among the risk factors for schizophrenia. Here we used a mouse model with chronic GSH deficit induced by knockout (KO) of the key GSH-synthesizing enzyme, glutamate-cysteine ligase modulatory subunit (GCLM).Methods With high-resolution magnetic resonance spectroscopy at 14.1 T, we determined the neurochemical profile of GCLM-KO, heterozygous, and wild-type mice in anterior cortex throughout development in a longitudinal study design.Results Chronic GSH deficit was accompanied by an elevation of glutamine (Gln), glutamate (Glu), Gln/Glu, N-acetylaspartate, myo-Inositol, lactate, and alanine. Changes were predominantly present at prepubertal ages (postnatal days 20 and 30). Treatment with N-acetylcysteine from gestation on normalized most neurochemical alterations to wild-type level.Conclusions Changes observed in GCLM-KO anterior cortex, notably the increase in Gln, Glu, and Gln/Glu, were similar to those reported in early schizophrenia, emphasizing the link between redox imbalance and the disease and validating the model. The data also highlight the prepubertal period as a sensitive time for redox-related neurochemical changes and demonstrate beneficial effects of early N-acetylcysteine treatment. Moreover, the data demonstrate the translational value of magnetic resonance spectroscopy to study brain disease in preclinical models.
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“In mice with a weakened GSH synthesis (Gclm KO mice), NAC prevents PVI and PNN deficits induced by an oxidative insult during postnatal development (Cabungcal et al., 2013a), although it does not increase GSH levels because of the Gclm deletion (das Neves Duarte et al., 2012).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as das Neves Duarte et al., 2012
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Cites
Introduction to Linear Regression Analysis.
Assunção, R., Sampson, P. D., Montgomery, D. C., & Peck, E. A. (1993) · Journal of the American Statistical Association · doi:10.2307/2290746 · Cited by 5,389
Krystal, J. H. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950030035004 · Cited by 3,330
Homayoun, H., & Moghaddam, B. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2213-07.2007 · Cited by 1,231
Schizophrenia as a Disorder of Neurodevelopment
Lewis, D. A., & Levitt, P. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142754 · Cited by 1,163
Patil, S. T., Zhang, L., Martenyi, F., Lowe, S. L., Jackson, K. A., Andreev, B. V., Avedisova, A. S., Bardenstein, L. M., Gurovich, I. Y., Morozova, M. A., et al. (2007) · Nature Medicine · doi:10.1038/nm1632 · Cited by 1,040
Prabakaran, S., SWATTON, J. E., Ryan, M. M., Huffaker, S. J., Huang, J.-J., Griffin, J. L., Wayland, M. T., Freeman, T., Dudbridge, F., Lilley, K. S., et al. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001511 · Cited by 985
Automatic, localized in Vivo adjustment of all first‐and second‐order shim coils
Gruetter, R. (1993) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910290613 · Cited by 875
Self-citationN-Acetylcysteine—a safe antidote for cysteine/glutathione deficiency
Atkuri, K. R., Mantovani, J. J., Herzenberg, L. A., & Herzenberg, L. A. (2007) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2007.04.005 · Cited by 721
Neuroinflammation, Oxidative Stress and the Pathogenesis of Alzheimers Disease
Agostinho, P., A. Cunha, R., & Oliveira, C. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210793176572 · Cited by 685 · cited 1×
“O xidative stress and impaired redox-regulation occur in neurodegenerative diseases such as Parkinson’s (1), Alzheimer’s (2), and Huntington disease (3), as well as in psychiatic pathologies including bipolar disorder (4) and schizophrenia (5).”
Food Intake, Water Intake, and Drinking Spout Side Preference of 28 Mouse Strains
Bachmanov, A. A., Reed, D. R., Beauchamp, G. K., & Tordoff, M. G. (2002) · Behavior Genetics · doi:10.1023/a:1020884312053 · Cited by 679
Research works printed but not linked: 2
- Do, 2010, Reverse translational approach to redox dysregulation in schizophrenia: Genetics, environment, neurodevelopment and therapy, Biol Psychiatry, 67, 199
- Cuenod, 2011, Redox dysregulation and oxidative stress affect parvalbumin interneurons and neural synchrony in anterior cingulated cortex during neurodevelopment, Schizophr Bull, 37, 102
Cited by
Sorted by citations
Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262
Self-citationSmaga, I., Niedzielska, E., Gawlik, M., Moniczewski, A., Krzek, J., Przegaliński, E., Pera, J., & Filip, M. (2015) · Pharmacological Reports · doi:10.1016/j.pharep.2014.12.015 · Cited by 252
Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuenod, M., & Do, K. Q. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.020 · Cited by 232
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Poels, E. M. P., Kegeles, L. S., Kantrowitz, J. T., Slifstein, M., Javitt, D. C., Lieberman, J. A., Abi-Dargham, A., & Girgis, R. R. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.136 · Cited by 205
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Cabungcal, J.-H., Counotte, D. S., Lewis, E. M., Tejeda, H. A., Piantadosi, P., Pollock, C., Calhoon, G. G., Sullivan, E. M., Presgraves, E., Kil, J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.028 · Cited by 204
Oxidative stress, prefrontal cortex hypomyelination and cognitive symptoms in schizophrenia
Maas, D. A., Vallès, A., & Martens, G. J. M. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.138 · Cited by 183
Oxidative stress and schizophrenia
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Fernandez, A., Meechan, D. W., Karpinski, B. A., Paronett, E. M., Bryan, C. A., Rutz, H. L. H., Radin, E. A., Lubin, N., Bonner, E. R., Popratiloff, A. S., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.013 · Cited by 168
Conus, P., Seidman, L. J., Fournier, M., Xin, L., Cleusix, M., Baumann, P., Ferrari, C., Cousins, A., Alameda, L., Gholam‐Rezaee, M., et al. (2017) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx093 · Cited by 164
Decreased Brain Levels of Vitamin B12 in Aging, Autism and Schizophrenia
Zhang, Y., Hodgson, N., Trivedi, M. S., Abdolmaleky, H. M., Fournier, M., Cuénod, M., Kim, Q., & Deth, R. C. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146797 · Cited by 164
Elevated brain lactate in schizophrenia: a 7 T magnetic resonance spectroscopy study
Rowland, L. M., Pradhan, S., Korenic, S. A., Wijtenburg, S. A., Hong, L. E., Edden, R. A. E., & Barker, P. B. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.239 · Cited by 160
Do, K. Q., Cuenod, M., & Hensch, T. K. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv065 · Cited by 158
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Hagihara, H., Catts, V. S., Katayama, Y., Shoji, H., Takagi, T., Huang, F. L., Nakao, A., Mori, Y., Huang, K., Ishii, S., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.167 · Cited by 147
Dwir, D., Giangreco, B., Xin, L., Tenenbaum, L., Cabungcal, J.-H., Steullet, P., Goupil, A., Cleusix, M., Jenni, R., Chtarto, A., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0393-5 · Cited by 140
Kulak, A., Steullet, P., Cabungcal, J.-H., Werge, T., Ingason, A., Cuenod, M., & Do, K. Q. (2013) · Antioxidants & Redox Signaling · doi:10.1089/ars.2012.4858 · Cited by 124
Self-citationTargeting of NMDA receptors in new treatments for schizophrenia
Hashimoto, K. (2014) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2014.934225 · Cited by 117
Das, T. K., Javadzadeh, A., Dey, A., Sabesan, P., Théberge, J., Raduà, J., & Palaniyappan, L. K. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.08.006 · Cited by 114
Duarte, J. M. N., Kim, Q., & Rolf Gruetter, A. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.01.135 · Cited by 108
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Eakin, K. C., Baratz-Goldstein, R., Pick, C. G., Zindel, O., Balaban, C. D., Hoffer, M. E., Lockwood, M. M., Miller, J. P., & Hoffer, B. J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0090617 · Cited by 106
Potential Roles of Redox Dysregulation in the Development of Schizophrenia
Perkins, D. O., Jeffries, C. D., & Do, K. Q. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.03.016 · Cited by 103
Rafiee, Z., García-Serrano, A. M., & Duarte, J. M. N. (2022) · Nutrients · doi:10.3390/nu14061292 · Cited by 105
A randomized placebo-controlled trial of an omega-3 fatty acid and vitamins E+C in schizophrenia
Bentsen, H., Osnes, K., Refsum, H., Solberg, D. K., & Bøhmer, T. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.110 · Cited by 97
Nucifora, L. G., Tanaka, T., Hayes, L. N., Kim, M., Lee, B. J., Matsuda, T., Nucifora, F. C., Sedlak, T. W., Mojtabai, R., Eaton, W. W., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.178 · Cited by 96
Kulak, A., Cuenod, M., & Do, K. Q. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.020 · Cited by 90
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Yao, J. K., & Reddy, R. D. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3646 · Cited by 76
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N‐acetylcysteine as a new prominent approach for treating psychiatric disorders
Smaga, I., Frankowska, M., & Filip, M. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15456 · Cited by 73
Duarte, J. M. N., & Xin, L. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2521-z · Cited by 69
Bustillo, J. (2013) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2013.15.3/jbustillo · Cited by 60
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Mahmoud, S., Moneim, A. E. A., Qayed, M. M., & El-Yamany, N. A. (2019) · Environmental Science and Pollution Research · doi:10.1007/s11356-019-05366-w · Cited by 54
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Robertson, O. D., Coronado, N. G., Sethi, R., Berk, M., & Dodd, S. (2019) · Early Intervention in Psychiatry · doi:10.1111/eip.12775 · Cited by 52
Xu, H., Zhang, H., Zhang, J., Huang, Q., Shen, Z., & Wu, R. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.09.027 · Cited by 58
Ribaudo, G., Bortoli, M., Pavan, C., Zagotto, G., & Orian, L. (2020) · Antioxidants · doi:10.3390/antiox9080714 · Cited by 51
Macêdo, D. S., de Lucena, D. F., Queiroz, A. I. G., Cordeiro, R. C., Araújo, M. M., Sousa, F. C., Vasconcelos, S. M., Hyphantis, T. N., Quevedo, J., McIntyre, R. S., et al. (2013) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2013.01.007 · Cited by 50
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Kätzel, D., Wolff, A. R., Bygrave, A. M., & Bannerman, D. M. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.486811 · Cited by 51
Khovarnagh, N., & Seyedalipour, B. (2021) · Saudi Pharmaceutical Journal · doi:10.1016/j.jsps.2021.02.004 · Cited by 47
Decreased Brain pH and Pathophysiology in Schizophrenia
Park, H. J., Choi, I., & Leem, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168358 · Cited by 48
Filho, A. J. M. C., Cunha, N. L., de Souza, A. G., Soares, M. V.-R., Jucá, P. M., de Queiroz, T., Oliveira, J. V. S., Valvassori, S. S., Barichello, T., Quevedo, J., et al. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.109872 · Cited by 46
Zhu, X., Cabungcal, J., Cuenod, M., Uliana, D., Do, K., & Grace, A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01198-8 · Cited by 41
Notaras, M. J., Lodhi, A., Barrio-Alonso, E., Foord, C., Rodrick, T. C., Jones, D. R., Fang, H., Greening, D. W., & Colak, D. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01189-9 · Cited by 45
Tran, T.-V., Shin, E., Jeong, J. H., Lee, J., Lee, Y., Jang, C., Nah, S.-Y., Lei, X. G., Toriumi, K., Yamada, K., et al. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0239-y · Cited by 42
Cardis, R., Cabungcal, J.-H., Dwir, D., Kim, Q., & Steullet, P. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.10.006 · Cited by 45
Corcoba, A., Steullet, P., Duarte, J. M. N., van de Looij, Y., Monin, A., Cuénod, M., Rolf Gruetter, A., & Kim, Q. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv110 · Cited by 40
Retsa, C., Knebel, J., Geiser, E., Ferrari, C., Jenni, R., Fournier, M., Alameda, L., Baumann, P., Clarke, S., Conus, P., et al. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.07.008 · Cited by 40
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Duarte, J. M. N., & Rolf Gruetter, A. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07688.x · Cited by 40
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Santos‐Silva, T., Colodete, D. A. E., Lisboa, J. R., Freitas, I. D. S., Lopes, C. F. B., Hadera, V., Lima, T. S. A., Souza, A. J., & Gomes, F. V. (2024) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13994 · Cited by 39
García-Serrano, A. M., Vieira, J. P. P., Fleischhart, V., & Duarte, J. M. N. (2022) · Nutritional Neuroscience · doi:10.1080/1028415x.2022.2131062 · Cited by 36
Repositioning drugs for traumatic brain injury - N-acetyl cysteine and Phenserine
Hoffer, B. J., Pick, C. G., Hoffer, M. E., Becker, R. E., Chiang, Y. H., & Greig, N. H. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0377-1 · Cited by 35
Durieux, A. M. S., Fernandes, C., Murphy, D., Labouesse, M. A., Giovanoli, S., Meyer, U., Li, Q., So, P., & McAlonan, G. M. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00343 · Cited by 34
Borella, V., Seeman, M. V., Cordeiro, R. C., Santos, J. V. D., de Souza, M. R. M., Fernandes, E. N. D. S., Monte, A. S., Vasconcelos, S. M. M., Quinn, J. P., de Lucena, D. F., et al. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22329 · Cited by 33
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Shungu, D. C. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.03.025 · Cited by 31
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Egerton, A. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05344-7 · Cited by 30
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Xin, L., & Tkáč, I. (2016) · Analytical Biochemistry · doi:10.1016/j.ab.2016.10.019 · Cited by 28
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Lee, M. R., Đenić, A., Hinton, D. J., Mishra, P. K., Choi, D., Pirko, I., Rodriguez, M., & Macura, S. I. (2012) · Bioanalysis · doi:10.4155/bio.12.129 · Cited by 27
Saleh, A. A. S. (2015) · The Journal of Basic and Applied Zoology · doi:10.1016/j.jobaz.2015.05.001 · Cited by 26
Girgis, R. R., Baker, S. C., Mao, X., Gil, R. B., Javitt, D. C., Kantrowitz, J. T., Gu, M., Spielman, D. M., Ojeil, N., Xu, X., et al. (2019) · Psychiatry Research · doi:10.1016/j.psychres.2019.03.018 · Cited by 26
Chakraborty, S., Rao, S., & Tripathi, S. J. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110527 · Cited by 25
Khoueiry, C. E., Cabungcal, J.-H., Rovó, Z., Fournier, M., Kim, Q., & Steullet, P. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01425-2 · Cited by 22
Lactate: a prospective target for therapeutic intervention in psychiatric disease
Cai, Y., Guo, H., Han, T., & Wang, H. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.387969 · Cited by 23
Tran, T.-V., Shin, E., Ko, S. K., Nam, Y., Chung, Y. H., Jeong, J. H., Jang, C., Nah, S.-Y., Yamada, K., Nabeshima, T., et al. (2016) · Journal of Medicinal Food · doi:10.1089/jmf.2016.3751 · Cited by 21
Rolland, B., Marche, K., Cottencin, O., & Bordet, R. (2012) · Schizophrenia Research and Treatment · doi:10.1155/2012/839853 · Cited by 20
LeVault, K. R., Tischkau, S. A., & Brewer, G. J. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150026 · Cited by 18
Schiavi, S., Rosa, P. L., Petrillo, S., Carbone, E., D’Amico, J., Piemonte, F., & Trezza, V. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.851679 · Cited by 19
Czekus, C., Steullet, P., López, A. O., Bozic, I., Rusterholz, T., Bandarabadi, M., Kim, Q., & Herrera, C. G. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01700-w · Cited by 18
Hagihara, H., Shoji, H., Hattori, S., Sala, G., Takamiya, Y., Tanaka, M., Ihara, M., Shibutani, M., Hatada, I., Hori, K., et al. (2023) · eLife · doi:10.7554/elife.89376 · Cited by 53
Santos‐Silva, T., Lopes, C. F. B., Ülgen, D. H., Guimarães, D. A., Guimarães, F. S., Alberici, L. C., Sandi, C., & Gomes, F. V. (2024) · Schizophrenia Bulletin · doi:10.1093/schbul/sbae033 · Cited by 20
N-acetylcysteine prevents increased amphetamine sensitivity in social isolation-reared mice
Herrmann, A. P., Benvenutti, R., Pilz, L. K., & Elisabetsky, E. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.03.012 · Cited by 18
Corcoba, A., Rolf Gruetter, A., Kim, Q., & Duarte, J. M. N. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14116 · Cited by 18
Oxidation and ubiquitination in neurodegeneration
Riederer, B. M., Leuba, G., & ElHajj, Z. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213488484 · Cited by 16
Lutgen, V., Qualmann, K. J., Resch, J. M., Kong, L., Choi, S., & Baker, D. L. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2926-3 · Cited by 16
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Lv, S., & Luo, C. (2024) · Molecular Medicine Reports · doi:10.3892/mmr.2024.13402 · Cited by 14
Reyes-Madrigal, F., León-Ortíz, P., Mao, X., Mora-Durán, R., Shungu, D. C., & de la Fuente‐Sandoval, C. (2019) · Archives of Medical Research · doi:10.1016/j.arcmed.2019.08.003 · Cited by 14
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Xin, L., Gambarota, G., Cudalbu, C., Mlynárik, V., & Rolf Gruetter, A. (2013) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-013-0378-3 · Cited by 14
Kim, S.-Y., Jang, E.-J., Hong, K. S., Lee, C., Lee, D., Choi, C., Lee, H.-S., & Choe, B. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0668-y · Cited by 14
Zhang, Y., Tong, L., Ma, L., Ye, H., Zeng, S., Zhang, S., Ding, Y., Wang, W., & Bao, T. (2024) · Advanced Biology · doi:10.1002/adbi.202300409 · Cited by 13
Simultaneous detection of glutathione and lactate using spectral editing at 3 T
Chan, K. L., Snoussi, K., Edden, R. A. E., & Barker, P. B. (2017) · NMR in Biomedicine · doi:10.1002/nbm.3800 · Cited by 13
Liang, J., Guan, X., Sun, Q., Hao, Y., & Xiu, M. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111092 · Cited by 11
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Pardhi, V. P., & Flora, S. J. S. (2020) · Biopharmaceutics & Drug Disposition · doi:10.1002/bdd.2252 · Cited by 12
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Sun, L., Fang, L., Lian, B., Xia, J.-J., Zhou, C., Wang, L., Mao, Q., Wang, X., Gong, X., Liang, Z., et al. (2016) · Molecular BioSystems · doi:10.1039/c6mb00651e · Cited by 10
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Rio, D. D., Stucchi, P., Hernández-Nuño, F., Cano, V., Morales, L., Chowen, J. A., Olmo, N. D., & Ruiz‐Gayo, M. (2016) · European Journal of Nutrition · doi:10.1007/s00394-016-1225-x · Cited by 8
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Hagihara, H., Shoji, H., Hattori, S., Sala, G., Takamiya, Y., Tanaka, M., Ihara, M., Shibutani, M., Hatada, I., Hori, K., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.02.428362 · Cited by 8
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Clari, R., McNamara, R. K., & Szeszko, P. R. (2020) · Springer eBooks · doi:10.1007/978-3-030-35206-6_19 · Cited by 3
Metadata
- Authors
- das Neves Duarte, J. M., Kulak, A., Gholam-Razaee, M. M., Cuenod, M., Gruetter, R., & Do, K. Q.
- Affiliations
- Centre Hospitalier Universitaire Vaudois (CH)
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2012-06
- Volume
- 71
- Issue
- 11
- Pages
- 1006-1014
- ISSN
- 0006-3223 (ISSN-L)
- OpenAlex
- W2171650204
- Cited by
- 124
- References
- 76
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 7 · 2023: 9 · 2022: 10 · 2021: 10 · 2020: 6 · 2019: 10 · 2018: 4 · 2017: 11 · 2016: 13 · 2015: 7 · 2014: 7 · 2013: 11 · 2012: 9
- FWCI
- 6.77
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- IRIS (submittedVersion)
- Lund University Publications (Lund University) (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Funders
- National Science Foundation (310030)
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (135736, 310030)
- Université de Genève
- Université de Lausanne
- Centre d'Imagerie BioMédicale
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Sulfur Compounds in Biology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- N-acetylcysteine, glutathione deficiency, schizophrenia, redox imbalance, neurochemical changes, glutamine, glutamate, N-acetylaspartate, myo-inositol, lactate, prepubertal development, anterior cortex, early treatment, mouse model
- MeSH terms
- Acetylcysteine, Alanine, Animals, Aspartic Acid, Cerebral Cortex, Disease Models, Animal, Glutamate-Cysteine Ligase, Glutamine, Glutathione, Inositol, Longitudinal Studies, Magnetic Resonance Spectroscopy, Schizophrenia, Free Radical Scavengers, Mice, Knockout, Glutamic Acid, Lactic Acid, Mice
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