Effect of Sertraline and Vortioxetine on Stress-Induced Brain Injury in Rats: Biochemical and Histopathological Evaluations

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Objectives: Our aim was to evaluate the comparative effects of sertraline and vortioxetine against stress-induced brain injury in rats. Methods: The rats were assigned to a nonstress group (NSG), stress-treated control (StC), sertraline + stress (SSt), and vortioxetine + stress (VSt) groups. Sertraline and vortioxetine (10 mg/kg) were given orally by gavage to the SSt and VSt groups. One hour later, all animals (except NSG) underwent forced immobilization to establish a stress model (2 hours). The drugs were given once a day for 30 days. The animals were killed with ketamine 150 mg/kg, and tissues were removed from the cerebral cortex. One-way analysis of variance and Fisher post hoc least significant difference were conducted for the analysis. Results: The malondialdehyde (nmol/mL) level was 2.58 ± 0.48 in the NSG, 8.09 ± 0.57 in the StC, 3.84 ± 0.53 in the SSt, and 2.84 ± 0.20 in the VSt group (P < 0.0002). The total glutathione (mmol/g) was 7.15 ± 0.59 in the NSG, 2.41 ± 0.43 in the StC, 4.58 ± 0.26 in the SSt, and 5.98 ± 0.13 in the VSt (P < 0.0002). The total oxidant status (mmol H2O2Eq/L) level was 3.56 ± 0.20 in the NSG, 9.99 ± 0.74 in the StC, 4.97 ± 0.39 in the SSt, and 3.81 ± 0.31 in the VSt (P < 0.0002). The total antioxidant status (mmolTroloxEq/L) level was 8.65 ± 0.37 in the NSG, 3.04 ± 0.22 in the StC, 6.29 ± 0.34 in the SSt, and 7.61 ± 0.40 in the VSt (P < 0.0002). Sertraline reduced pericellular edema in astrocytes and oligodendrocytes and decreased perivascular edema, dilatation, and congestion of blood vessels, whereas these were not seen with vortioxetine. Conclusions: Compared with sertraline, vortioxetine is a neuroprotective antidepressant with higher antioxidant activity and can more effectively prevent stress-induced brain tissue injury. Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

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AlanDeğerDil
dc.contributor.authorCim, Emine Fusun Akyuz
dc.contributor.authorSuleyman, Zeynep
dc.contributor.authorSuleyman, Halis
dc.contributor.authorYazici, Gulce Naz
dc.contributor.authorCoban, Taha Abdulkadir
dc.date.accessioned2026-10-18T20:26:07.690959718Z
dc.date.available2026-10-18T20:26:07.690959718Z
dc.date.issued2024
dc.description.abstractObjectives: Our aim was to evaluate the comparative effects of sertraline and vortioxetine against stress-induced brain injury in rats. Methods: The rats were assigned to a nonstress group (NSG), stress-treated control (StC), sertraline + stress (SSt), and vortioxetine + stress (VSt) groups. Sertraline and vortioxetine (10 mg/kg) were given orally by gavage to the SSt and VSt groups. One hour later, all animals (except NSG) underwent forced immobilization to establish a stress model (2 hours). The drugs were given once a day for 30 days. The animals were killed with ketamine 150 mg/kg, and tissues were removed from the cerebral cortex. One-way analysis of variance and Fisher post hoc least significant difference were conducted for the analysis. Results: The malondialdehyde (nmol/mL) level was 2.58 ± 0.48 in the NSG, 8.09 ± 0.57 in the StC, 3.84 ± 0.53 in the SSt, and 2.84 ± 0.20 in the VSt group (P < 0.0002). The total glutathione (mmol/g) was 7.15 ± 0.59 in the NSG, 2.41 ± 0.43 in the StC, 4.58 ± 0.26 in the SSt, and 5.98 ± 0.13 in the VSt (P < 0.0002). The total oxidant status (mmol H2O2Eq/L) level was 3.56 ± 0.20 in the NSG, 9.99 ± 0.74 in the StC, 4.97 ± 0.39 in the SSt, and 3.81 ± 0.31 in the VSt (P < 0.0002). The total antioxidant status (mmolTroloxEq/L) level was 8.65 ± 0.37 in the NSG, 3.04 ± 0.22 in the StC, 6.29 ± 0.34 in the SSt, and 7.61 ± 0.40 in the VSt (P < 0.0002). Sertraline reduced pericellular edema in astrocytes and oligodendrocytes and decreased perivascular edema, dilatation, and congestion of blood vessels, whereas these were not seen with vortioxetine. Conclusions: Compared with sertraline, vortioxetine is a neuroprotective antidepressant with higher antioxidant activity and can more effectively prevent stress-induced brain tissue injury. Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.
dc.identifier.doi10.1097/wnf.0000000000000615
dc.identifier.eissn1537-162X
dc.identifier.endpage217
dc.identifier.issn0362-5664
dc.identifier.issue6
dc.identifier.pmid39792536
dc.identifier.scopus2-s2.0-85210353288
dc.identifier.startpage213
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11021
dc.identifier.volume47
dc.identifier.wosWOS:001361328000002
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofClinical Neuropharmacology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantioxidant
dc.subjectbrain injury
dc.subjectoxidant
dc.subjectoxidative stress
dc.subjectsertraline
dc.subjectstress
dc.subjectvortioxetine
dc.subjectAnimals
dc.subjectBrain
dc.subjectBrain Injuries
dc.subjectDisease Models, Animal
dc.subjectGlutathione
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectSelective Serotonin Reuptake Inhibitors
dc.subjectStress, Psychological
dc.subjectketamine
dc.subjectmalonaldehyde
dc.subjectserotonin uptake inhibitor
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectastrocyte
dc.subjectbrain biochemistry
dc.subjectbrain protection
dc.subjectcerebral cortical tissue
dc.titleEffect of Sertraline and Vortioxetine on Stress-Induced Brain Injury in Rats: Biochemical and Histopathological Evaluations
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos1
rdl.departmentDepartment of Nursing, Erzincan Binali Yıldırım University Faculty of Health Sciences. | Medical Biochemistry, Erzincan Binali Yıldırım University Faculty of Medicine, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)