Effect of tangeretin on cisplatin-induced oxido-inflammatory brain damage in rats

ArticleAçık Erişim

Özet

Cisplatin (CIS) is a platinum-derived chemotherapeutic agent commonly utilized in the treatment of various malignant tumours. However, anticancer doses of the drug cause serious damage to the brain. This study aimed to determine the potential protective effects of tangeretin, which has antioxidant and anti-inflammatory properties, in cisplatin-induced neurotoxicity on BALB/c mice brains. Male BALB/c mice were randomized and separated into four groups. Tangeretin was given for 10 days by gavage. CIS was injected as a single dose of 10 mg/kg intraperitoneally (ip) on the 10th day. Brain tissues, malondialdehyde (MDA), total glutathione (tGSH), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase (CAT) and nitric oxide (NO) levels were measured to determine oxidative damage and myeloperoxidase, tumour necrosis factor-alpha (TNF-α), interleukin 1 beta (IL-1β), IL-6 and IL-10 were measured to determine inflammatory activity. In addition, 8-OHdG and caspase-3 were analysed by immunofluorescence methods. While CIS administration remarkably elevated reactive oxygen species, MDA, and NO levels in brain tissue compared to the control, tGSH, GPx, SOD and CAT levels were significantly decreased. Also, it has been detected that TNF-α, IL-1β and IL-6 obtained in CIS-treated groups increased as well as IL-10 decreased, thereby elevating the inflammatory response. In addition, 8-OHdG and caspase-3 immunoreactivity in neurons increased with CIS administration. Treatment with tangeretin ameliorated the deterioration in oxidant/antioxidant status, overpowered neuroinflammation and ameliorated neurotoxicity-induced apoptosis. This study shows that tangeretin has beneficial effects on CIS-induced neurodegeneration. Possible mechanisms underlying these beneficial effects include the antioxidant and anti-inflammatory properties of tangeretin. © 2024 The Author(s). Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11512Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/jcmm.18565Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorCicek, Betul
dc.contributor.authorDanisman, Betul
dc.contributor.authorBolat, Ismail
dc.contributor.authorKiliclioglu, Metin
dc.contributor.authorKuzucu, Mehmet
dc.contributor.authorSuleyman, Halis
dc.contributor.authorTsarouhas, Konstantinos
dc.contributor.authorTsatsakis, Aristidis
dc.contributor.authorTaghizadehghalehjoughi, Ali
dc.date.accessioned2026-10-18T20:26:33.219531853Z
dc.date.available2026-10-18T20:26:33.219531853Z
dc.date.issued2024
dc.description.abstractCisplatin (CIS) is a platinum-derived chemotherapeutic agent commonly utilized in the treatment of various malignant tumours. However, anticancer doses of the drug cause serious damage to the brain. This study aimed to determine the potential protective effects of tangeretin, which has antioxidant and anti-inflammatory properties, in cisplatin-induced neurotoxicity on BALB/c mice brains. Male BALB/c mice were randomized and separated into four groups. Tangeretin was given for 10 days by gavage. CIS was injected as a single dose of 10 mg/kg intraperitoneally (ip) on the 10th day. Brain tissues, malondialdehyde (MDA), total glutathione (tGSH), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase (CAT) and nitric oxide (NO) levels were measured to determine oxidative damage and myeloperoxidase, tumour necrosis factor-alpha (TNF-α), interleukin 1 beta (IL-1β), IL-6 and IL-10 were measured to determine inflammatory activity. In addition, 8-OHdG and caspase-3 were analysed by immunofluorescence methods. While CIS administration remarkably elevated reactive oxygen species, MDA, and NO levels in brain tissue compared to the control, tGSH, GPx, SOD and CAT levels were significantly decreased. Also, it has been detected that TNF-α, IL-1β and IL-6 obtained in CIS-treated groups increased as well as IL-10 decreased, thereby elevating the inflammatory response. In addition, 8-OHdG and caspase-3 immunoreactivity in neurons increased with CIS administration. Treatment with tangeretin ameliorated the deterioration in oxidant/antioxidant status, overpowered neuroinflammation and ameliorated neurotoxicity-induced apoptosis. This study shows that tangeretin has beneficial effects on CIS-induced neurodegeneration. Possible mechanisms underlying these beneficial effects include the antioxidant and anti-inflammatory properties of tangeretin. © 2024 The Author(s). Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.
dc.identifier.doi10.1111/jcmm.18565
dc.identifier.issn1582-1838
dc.identifier.issue14
dc.identifier.pmcidPMC11265995
dc.identifier.pmid39044287
dc.identifier.scopus2-s2.0-85199291123
dc.identifier.startpagee18565
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11512
dc.identifier.volume28
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofJournal of Cellular and Molecular Medicine
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectanti-inflammatory
dc.subjectantioxidant
dc.subjectcisplatin
dc.subjectoxidant/antioxidant status
dc.subjecttangeretin
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents
dc.subjectAntioxidants
dc.subjectBrain
dc.subjectCytokines
dc.subjectFlavones
dc.subjectGlutathione
dc.subjectGlutathione Peroxidase
dc.subjectMale
dc.subjectMalondialdehyde
dc.subjectMice
dc.subjectMice, Inbred BALB C
dc.subjectNitric Oxide
dc.subjectOxidative Stress
dc.subjectRats
dc.subjectReactive Oxygen Species
dc.subjectSuperoxide Dismutase
dc.subjectcaspase 3
dc.subjectcatalase
dc.subjectdimethyl sulfoxide
dc.subjectglutathione reductase
dc.subjectinterleukin 10
dc.subjectinterleukin 1beta
dc.subjectinterleukin 6
dc.subjectmalonaldehyde
dc.titleEffect of tangeretin on cisplatin-induced oxido-inflammatory brain damage in rats
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus16
rdl.departmentDepartment of Physiology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey. | Department of Biology, Faculty of Arts and Sciences, Erzincan Binali Yildirim University, Erzincan, Turkey. | Department of Medical Pharmacology, Faculty of Medicine, Erzincan Binali Yildirim University, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexPUBMED