In Vivo Evidence for the Preventive Role of Vaccinium macrocarpon Aiton in Indomethacin-Induced Gastric Ulcer: Focusing on Antioxidant, Anti-Inflammatory and Anti-Apoptotic Mechanisms

ArticleAçık Erişim

Özet

The present study aimed to unveil the gastroprotective potential of Vaccinium macrocarpon (VM) extract and its mechanism of action against indomethacin (INDO)-induced gastric ulcers in rats. To achieve this goal, rats were pretreated with either omeprazole (20 mg/kg) or VM (100 mg/kg) orally for 14 consecutive days. Gastric tissue samples were collected and various parameters were evaluated to understand the mechanism of VM's action, including the levels of superoxide dismutase, malondialdehyde, glutathione, CAT and transforming growth factor beta (TGF-β), as well as the mRNA expression levels of tumour necrosis factor alpha, interleukin 1 beta, nuclear factor kappa B (NF-κB) and inhibitor kappa B (IκB). Additionally, the immunopositivity of cyclooxygenase (COX)-1, COX-2, PGE2, proliferating cell nuclear antigen (PCNA) and caspase-3 was assessed. The total amount of phenolic compounds present in the VM extract was high (58.08 µg/mL gallic acid equivalent/mg extract). The healing effect of VM was demonstrated by an increase in the expression of PCNA. Furthermore, the level of TGF-β was found to increase upon treatment with VM. Analyses of COX-1, COX-2 and PGE2 expression in gastric tissue confirmed the gastroprotective effect of VM. Notably, the expression of NF-κB was markedly reduced, whereas that of IκB was substantially increased. Overall, the findings of this study demonstrate that VM extract has gastroprotective and curative effects against INDO-induced ulcers through its antioxidant, anti-inflammatory, mucosal regenerative and anti-apoptotic activities. Therefore, VM may serve as a useful adjuvant treatment for nonsteroidal anti-inflammatory drugs–induced gastric ulcer disease. © 2025 The Author(s). Veterinary Medicine and Science published by John Wiley & Sons Ltd.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11034Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/vms3.70048Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorAydin, Ismail Cagri
dc.contributor.authorFerah Okkay, Irmak
dc.contributor.authorOkkay, Ufuk
dc.contributor.authorOzkaraca, Mustafa
dc.contributor.authorYesilyurt, Fatma
dc.contributor.authorYilmaz, Aysegul
dc.contributor.authorCicek, Betul
dc.contributor.authorKaratas, Ozhan
dc.contributor.authorKalkandelen, Hilal Kadioglu
dc.contributor.authorAydin, Bilge
dc.contributor.authorHacimuftuoglu, Ahmet
dc.contributor.authorKarakaya, Songul
dc.contributor.authorGüvenalp, Zuhal
dc.contributor.authorAbd El-Aty, A.M.
dc.date.accessioned2026-10-18T20:26:08.370413062Z
dc.date.available2026-10-18T20:26:08.370413062Z
dc.date.issued2025
dc.description.abstractThe present study aimed to unveil the gastroprotective potential of Vaccinium macrocarpon (VM) extract and its mechanism of action against indomethacin (INDO)-induced gastric ulcers in rats. To achieve this goal, rats were pretreated with either omeprazole (20 mg/kg) or VM (100 mg/kg) orally for 14 consecutive days. Gastric tissue samples were collected and various parameters were evaluated to understand the mechanism of VM's action, including the levels of superoxide dismutase, malondialdehyde, glutathione, CAT and transforming growth factor beta (TGF-β), as well as the mRNA expression levels of tumour necrosis factor alpha, interleukin 1 beta, nuclear factor kappa B (NF-κB) and inhibitor kappa B (IκB). Additionally, the immunopositivity of cyclooxygenase (COX)-1, COX-2, PGE2, proliferating cell nuclear antigen (PCNA) and caspase-3 was assessed. The total amount of phenolic compounds present in the VM extract was high (58.08 µg/mL gallic acid equivalent/mg extract). The healing effect of VM was demonstrated by an increase in the expression of PCNA. Furthermore, the level of TGF-β was found to increase upon treatment with VM. Analyses of COX-1, COX-2 and PGE2 expression in gastric tissue confirmed the gastroprotective effect of VM. Notably, the expression of NF-κB was markedly reduced, whereas that of IκB was substantially increased. Overall, the findings of this study demonstrate that VM extract has gastroprotective and curative effects against INDO-induced ulcers through its antioxidant, anti-inflammatory, mucosal regenerative and anti-apoptotic activities. Therefore, VM may serve as a useful adjuvant treatment for nonsteroidal anti-inflammatory drugs–induced gastric ulcer disease. © 2025 The Author(s). Veterinary Medicine and Science published by John Wiley & Sons Ltd.
dc.identifier.doi10.1002/vms3.70048
dc.identifier.issn2053-1095
dc.identifier.issue1
dc.identifier.pmcidPMC11694502
dc.identifier.pmid39745481
dc.identifier.scopus2-s2.0-85213804335
dc.identifier.startpagee70048
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11034
dc.identifier.volume11
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofVeterinary Medicine and Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcyclooxygenase (COX)
dc.subjectnuclear factor kappa B (NF-κB)/inhibitor kappa B (IκB)
dc.subjectoxidative stress
dc.subjectulcer
dc.subjectvaccinium macrocarpon
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents
dc.subjectAnti-Ulcer Agents
dc.subjectAntioxidants
dc.subjectApoptosis
dc.subjectIndomethacin
dc.subjectMale
dc.subjectPlant Extracts
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectRats, Wistar
dc.subjectStomach Ulcer
dc.subjectantiinflammatory agent
dc.subjectantioxidant
dc.subjectcaspase 3
dc.subjectcatalase
dc.subjectcycline
dc.subjectcyclooxygenase 1
dc.subjectcyclooxygenase 2
dc.subjectglutathione
dc.subjectI kappa B
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectinterleukin 1beta
dc.subjectmalonaldehyde
dc.subjectmessenger RNA
dc.titleIn Vivo Evidence for the Preventive Role of Vaccinium macrocarpon Aiton in Indomethacin-Induced Gastric Ulcer: Focusing on Antioxidant, Anti-Inflammatory and Anti-Apoptotic Mechanisms
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus5
rdl.departmentDepartment of Pharmacology, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, Turkey. | Department of Physiology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey. | Department of Pharmacognosy, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexPUBMED