The Impact of Resveratrol on Oxidative Stress Induced by Methotrexate in Rat Ileum Tissue: Evaluation of Biochemical and Histopathological Features and Analysis of Gene Expression

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Objective: The aim of this study was to assess the impact of resveratrol (RST) on oxidative stress induced by methotrexate in rat ileum tissue. Materials and Methods: Twenty-four rats were divided into 4 groups with 6 in each group. Each rat was orally administered the following every day for 30 days: group 1 (MTXG), methotrexate (MTX; 5 mg/kg); group 2 (RMTXG), MTX (5 mg/kg) plus RST (25 mg/kg/day); group 3 (RSTG), RST alone (25 mg/kg/day), and group 4 (controls), distilled water. After the rats had been sacrified, the ilea were removed for the assessment of malondialdehyde (MDA), total glutathione (tGSH) and glutathione peroxidase (GSH-Px). Gene expression analyses for interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α) and myeloperoxidase (MPO) were also performed. Hematoxylin and eosin-stained paraffin-embedded sections of the ileum were analyzed under a light microscope and the findings were recorded. Statistical analyses of the data were performed using one-way ANOVA. Results: The administration of MTX in group 1 yielded a higher level of MDA (8.33 ± 2.5 μmol/g protein, p < 0.001) and lower levels of tGSH (0.97 ± 0.29 nmol/g protein) and GSH-Px (5.22 ± 0.35 U/g protein, p < 0.001) compared to the other groups. MTX also increased IL-1β (40.33 ± 5.43 gene expression levels), TNF-α (6.08 ± 0.59) and MPO gene expression (9 ± 1.41) in group 1 compared to the controls (11.33 ± 2.07, 2.15 ± 0.33 and 3.43 ± 0.48, respectively, p < 0.001). The impact of RST on IL-1β, TNF-α and MPO gene expression induced by MTX was observed as a reversal of these findings (p < 0.05). Severe inflammation, damage to the villus epithelium and crypt necrosis was observed histopathologically in the MTXG group, whereas only mild inflammation was seen in the RMTXG group. Conclusion: In this study, ileal damage caused by MTX was inhibited by RST. © 2015 S. Karger AG, Basel.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15363Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1159/000442020Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorOzcicek, Adalet
dc.contributor.authorCetin, Nihal
dc.contributor.authorKeskin Cimen, Ferda
dc.contributor.authorTumkaya, Levent
dc.contributor.authorMalkoc, Ismail
dc.contributor.authorGulaboglu, Mine
dc.contributor.authorYarali, Oguzhan
dc.contributor.authorSuleyman, Bahadir
dc.date.accessioned2026-10-18T20:30:10.875938011Z
dc.date.available2026-10-18T20:30:10.875938011Z
dc.date.issued2016
dc.description.abstractObjective: The aim of this study was to assess the impact of resveratrol (RST) on oxidative stress induced by methotrexate in rat ileum tissue. Materials and Methods: Twenty-four rats were divided into 4 groups with 6 in each group. Each rat was orally administered the following every day for 30 days: group 1 (MTXG), methotrexate (MTX; 5 mg/kg); group 2 (RMTXG), MTX (5 mg/kg) plus RST (25 mg/kg/day); group 3 (RSTG), RST alone (25 mg/kg/day), and group 4 (controls), distilled water. After the rats had been sacrified, the ilea were removed for the assessment of malondialdehyde (MDA), total glutathione (tGSH) and glutathione peroxidase (GSH-Px). Gene expression analyses for interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α) and myeloperoxidase (MPO) were also performed. Hematoxylin and eosin-stained paraffin-embedded sections of the ileum were analyzed under a light microscope and the findings were recorded. Statistical analyses of the data were performed using one-way ANOVA. Results: The administration of MTX in group 1 yielded a higher level of MDA (8.33 ± 2.5 μmol/g protein, p < 0.001) and lower levels of tGSH (0.97 ± 0.29 nmol/g protein) and GSH-Px (5.22 ± 0.35 U/g protein, p < 0.001) compared to the other groups. MTX also increased IL-1β (40.33 ± 5.43 gene expression levels), TNF-α (6.08 ± 0.59) and MPO gene expression (9 ± 1.41) in group 1 compared to the controls (11.33 ± 2.07, 2.15 ± 0.33 and 3.43 ± 0.48, respectively, p < 0.001). The impact of RST on IL-1β, TNF-α and MPO gene expression induced by MTX was observed as a reversal of these findings (p < 0.05). Severe inflammation, damage to the villus epithelium and crypt necrosis was observed histopathologically in the MTXG group, whereas only mild inflammation was seen in the RMTXG group. Conclusion: In this study, ileal damage caused by MTX was inhibited by RST. © 2015 S. Karger AG, Basel.
dc.identifier.doi10.1159/000442020
dc.identifier.eissn1423-0151
dc.identifier.endpage186
dc.identifier.issn1011-7571
dc.identifier.issue2
dc.identifier.pmcidPMC5588348
dc.identifier.pmid26517535
dc.identifier.scopus2-s2.0-84958106515
dc.identifier.startpage181
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15363
dc.identifier.volume25
dc.identifier.wosWOS:000370081000014
dc.language.isoen
dc.publisherS. Karger AG
dc.relation.ispartofMedical Principles and Practice
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGene expression
dc.subjectIleum tissue
dc.subjectOxidative stress
dc.subjectRat
dc.subjectResveratrol
dc.subjectAnalysis of Variance
dc.subjectAnimals
dc.subjectAntioxidants
dc.subjectFemale
dc.subjectGlutathione Peroxidase
dc.subjectIleal Diseases
dc.subjectIleum
dc.subjectInterleukin-1beta
dc.subjectMale
dc.subjectMethotrexate
dc.subjectPeroxidase
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectTumor Necrosis Factor-alpha
dc.subjecteosin
dc.subjectglutathione
dc.subjecthematoxylin
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectmyeloperoxidase
dc.subjectparaffin
dc.subjecttumor necrosis factor alpha
dc.subjectantioxidant
dc.subjecttumor necrosis factor
dc.subjectanimal experiment
dc.titleThe Impact of Resveratrol on Oxidative Stress Induced by Methotrexate in Rat Ileum Tissue: Evaluation of Biochemical and Histopathological Features and Analysis of Gene Expression
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus13
rdl.citation.wos12
rdl.departmentDepartment of Internal Medicine, Faculty of Medicine, Erzincan University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)