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Increased malondialdehyde and nitric oxide formation, lowered total radical trapping capacity coupled with psychological stressors are strongly associated with the phenome of first-episode mild depression in undergraduate students.

Authors :
Brinholi FF
Vasupanrajit A
Semeão LO
Michelin AP
Matsumoto AK
Almulla AF
Tunvirachaisakul C
Barbosa DS
Maes M
Source :
Neuroscience [Neuroscience] 2024 Aug 30; Vol. 554, pp. 52-62. Date of Electronic Publication: 2024 Jul 09.
Publication Year :
2024

Abstract

Undergraduate students are frequently afflicted by major depressive disorder (MDD). Oxidative and nitrosative stress (O&NS) has been implicated in the pathophysiology of MDD. There is no information regarding whether mild outpatient MDD (SDMD) and first episode SDMD (FE-SDMD) are accompanied by O&NS. The current study compared lipid hydroperoxides (LOOH), malondialdehyde (MDA), advanced protein oxidation products, nitric oxide metabolites (NOx), thiol groups, plasma total antioxidant potential (TRAP), and paraoxonase 1 activities among SDMD and FE-SDMD patients versus healthy controls. We found that SDMD and FE-SDMD exhibit elevated MDA and NOx, and decreased TRAP and LOOH as compared with controls. There was a significant and positive correlation between O&NS biomarkers and adverse childhood experiences (ACEs), and negative life events (NLEs). O&NS pathways, NLEs and ACEs accounted for 51.7 % of the variance in the phenome of depression, and O&NS and NLS explained 42.9 % of the variance in brooding. Overall, these results indicate that SDMD and FE-SDMD are characterized by reduced total antioxidant defenses and increased aldehyde and NOx production. The combined effects of oxidative and psychological stressors are substantially associated with the manifestation of SDMD.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 IBRO. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-7544
Volume :
554
Database :
MEDLINE
Journal :
Neuroscience
Publication Type :
Academic Journal
Accession number :
38992564
Full Text :
https://doi.org/10.1016/j.neuroscience.2024.06.003