The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Altered glutathione redox state in schizophrenia.
Open accessAbstract
Altered antioxidant status has been reported in schizophrenia. The glutathione (GSH) redox system is important for reducing oxidative stress. GSH, a radical scavenger, is converted to oxidized glutathione (GSSG) through glutathione peroxidase (GPx), and converted back to GSH by glutathione reductase (GR). Measurements of GSH, GSSG and its related enzymatic reactions are thus important for evaluating the redox and antioxidant status. In the present study, levels of GSH, GSSG, GPx and GR were assessed in the caudate region of postmortem brains from schizophrenic patients and control subjects (with and without other psychiatric disorders). Significantly lower levels of GSH, GPx, and GR were found in schizophrenic group than in control groups without any psychiatric disorders. Concomitantly, a decreased GSH:GSSG ratio was also found in schizophrenic group. Moreover, both GSSG and GR levels were significantly and inversely correlated to age of schizophrenic patients, but not control subjects. No significant differences were found in any GSH redox measures between control subjects and individuals with other types of psychiatric disorders. There were, however, positive correlations between GSH and GPx, GSH and GR, as well as GPx and GR levels in control subjects without psychiatric disorders. These positive correlations suggest a dynamic state is kept in check during the redox coupling under normal conditions. By contrast, lack of such correlations in schizophrenia point to a disturbance of redox coupling mechanisms in the antioxidant defense system, possibly resulting from a decreased level of GSH as well as age‐related decreases of GSSG and GR activities.
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?
In the citing paper
“Redox dysregulation has been observed in schizophrenic patients, who have defective antioxidant systems and exhibit increased lipid peroxidation (Do et al., 2000; Yao et al., 2006; Flatow et al., 2013).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Yao et al., 2006
In the citing paper
“Higher levels of oxidative stress have been reported in schizophrenia (Wang et al, 2009;Yao et al, 2006)”
From Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia (2016) · cites this paper as Yao et al, 2006
In the citing paper
“In an animal model with low GSH content, as reported in the brain of some schizophrenia patients (Do et al., 2000; Gawryluk et al., 2011; Yao et al., 2006), there is a deficit in prefrontal and hippocampal PVI, impairing high-frequency neuronal synchronization (Cabungcal et al., 2013a; Cabungcal et al., 2013b; Steullet et al., 2010).”
From Redox dysregulation, neuroinflammation, and NMDA receptor hypofunction: A “central hub” in schizophrenia pathophysiology? (2016) · cites this paper as Yao et al., 2006
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
Diagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,845
Free-Radical Chemistry of Cigarette Smoke and Its Toxicological Implications
CHURCH, D. F., & PRYOR, W. A. (1985) · Environmental Health Perspectives · doi:10.1289/ehp.8564111 · Cited by 1,442
Selective Modification of Glutathione Metabolism
Meister, A. (1983) · Science · doi:10.1126/science.6836290 · Cited by 1,267 · cited 1×
“Its reducing and nucleophilic properties protect cells against destructive effects of reactive oxygen species and free radicals [12].”
Oxidants in Cigarette Smoke Radicals, Hydrogen Peroxide, Peroxynitrate, and Peroxynitritea
Pryor, W. A., & Stone, K. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb39148.x · Cited by 1,179
Prevalence of smoking among psychiatric outpatients
(1986) · American Journal of Psychiatry · doi:10.1176/ajp.143.8.993 · Cited by 1,058
Glutathione: an overview of biosynthesis and modulation
Anderson, M. E. (1998) · Chemico-Biological Interactions · doi:10.1016/s0009-2797(97)00146-4 · Cited by 917
Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo
Do, K. Q., Trabesinger, A. H., Kirsten‐Krüger, M., Lauer, C. J., Dydak, U., Hell, D., Holsboer, F., Boesiger, P., & Cuénod, M. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00229.x · Cited by 540
Forman, H. J., Fukuto, J. M., & Torrès, M. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00516.2003 · Cited by 533
Lung glutathione and oxidative stress: implications in cigarette smoke-induced airway disease
Rahman, I., & MacNee, W. (1999) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1999.277.6.l1067 · Cited by 420
Kinetics of Nitrosation of Thiols by Nitric Oxide in the Presence of Oxygen
Kharitonov, V. G., Sundquist, A. R., & Sharma, V. S. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.47.28158 · Cited by 365
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–320 of 320
Estrés Oxidativo y Esquizofrenia
Prados, A. B. (2014) · Gredos (University of Salamanca) · doi:10.14201/gredos.124073
Gautam, A. H. (2010) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t30c4vjx
Neuhaus, D. (2015) · Common Library Network (Der Gemeinsame Bibliotheksverbund)
Oxidative and nitrative stress in schizophrenia
Dietrich‐Muszalska, A. (2016) · Wiley eBooks · doi:10.1002/9781118832431.ch5
Zhou, X. (2018) · D-Scholarship@Pitt (University of Pittsburgh)
Rogóż, Z., Lech, M. A., Chamera, K., & Wąsik, A. (2022) · Neurotoxicity Research · doi:10.1007/s12640-022-00496-5
Metabolic stress and antipsychotic treatment induced gene expression alterations in human cell
Kálmán, S. (2016) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2988
Faculty Opinions recommendation of Meta-analysis of oxidative stress in schizophrenia.
Altamura, A. C., & Buoli, M. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718074530.793484196
Complementary/Integrative Medicine Treatment and Prevention of Youth Psychosis
Bhatara, V. S., Daniel, J., Whitman, C., Vik, T., Bernstein, B., & Simkin, D. R. (2023) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2022.08.009
Mekkawy, M. H., Karam, H. M., Mohamed, M. A. E. H., & Lotfy, D. M. (2023) · Dose-Response · doi:10.1177/15593258231217845
Samuelsson, M. (2012) · KTH Publication Database DiVA (KTH Royal Institute of Technology)
Arif Malik, S. S. (2017) · International Journal of Biosciences (IJB) · doi:10.12692/ijb/11.2.125-135
Rogóż, Z., & Wąsik, A. (2026) · Pharmacological Reports · doi:10.1007/s43440-026-00853-7
Ebrahimi, M. N., Banazadeh, M., Kohlmeier, K. A., & Shabani, M. (2026) · The Neuroscientist · doi:10.1177/10738584261445364
Rouhani, M. H., Navab, F. S., Shahdadian, F., & Keyhanpour, S. (2026) · SpringerBriefs in modern perspectives on disability research. · doi:10.1007/978-981-95-8150-4_9
Thirumalai, J., Mohammed, A. A. F., & Jeslin, G. N. (2026) · SN Comprehensive Clinical Medicine · doi:10.1007/s42399-026-02557-8
The Role of Cytochrome P450 Holoenzyme Metabolism in the Origin of Neuropathologies
Štambuk, S. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27156971
Energetic dysregulations in psychotic disorders: Targets for new therapeutics
Anderson, J., Sonntag, K., Le, T. D. V., Shannon, K., Wang, C., Du, F., Chen, X., McPhie, D. L., Öngür, D., Cohen, B. M., et al. (2026) · FEBS Journal · doi:10.1111/febs.70719
Manvini., S., & Verma, P. (2026) · Asian Journal of Research in Pharmaceutical Sciences · doi:10.52711/2231-5659.2026.00052
Metadata
- Authors
- Yao, J. K., Leonard, S., & Reddy, R.
- Affiliations
- University of Pittsburgh (US)
- Denver VA Medical Center (US)
- VA Pittsburgh Healthcare System (US)
- Corresponding author
- Yao, Jeffrey K.
- ORCID
- Reddy, Ravinder
- Venue
- Disease Markers
- Publisher
- Wiley
- Published
- 2006-01
- Volume
- 22
- Issue
- 1-2
- Pages
- 83-93
- ISSN
- 0278-0240 (ISSN-L)
- 1875-8630
- PMC
- PMC3850558
- OpenAlex
- W2088215062
- Cited by
- 321
- References
- 45
- Citations by year
- 2026: 11 · 2025: 9 · 2024: 6 · 2023: 10 · 2022: 20 · 2021: 20 · 2020: 10 · 2019: 16 · 2018: 19 · 2017: 18 · 2016: 18 · 2015: 21 · 2014: 12 · 2013: 18 · 2012: 21
- FWCI
- 6.18
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Disease Markers (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH58141, MH64118, DA09457)
- Brain and Behavior Research Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- schizophrenia, glutathione, glutathione disulfide, glutathione peroxidase, glutathione reductase, GSH/GSSG ratio, oxidative stress, antioxidant defense, redox coupling, caudate nucleus, postmortem brain, age-related decline
- MeSH terms
- Age Factors, Aged, Caudate Nucleus, Female, Glutathione, Glutathione Reductase, Humans, Male, Middle Aged, Oxidation-Reduction, Schizophrenia, Sex Factors, Smoking, Glutathione Disulfide
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