Protective effect of lycopene against ochratoxin A induced renal oxidative stress and apoptosis in rats

dc.contributor.authorPalabiyik, S. Sezin
dc.contributor.authorErkekoglu, Pinar
dc.contributor.authorZeybek, N. Dilara
dc.contributor.authorKizilgun, Murat
dc.contributor.authorBaydar, Dilek Ertoy
dc.contributor.authorSahin, Gonul
dc.contributor.authorGiray, Belma Kocer
dc.date.accessioned2026-02-06T18:38:03Z
dc.date.issued2013
dc.departmentDoğu Akdeniz Üniversitesi
dc.description.abstractThis study was designed to investigate the possible protective effect of lycopene against the renal toxic effects of OTA. Male Sprague-Dawley rats (<200 g, n = 6) were treated with OTA (0.5 mg/kg/day) and/or lycopene (5 mg/kg/day) by gavage for 14 days. Histopathological examinations were performed and apoptotic cell death in both cortex and medulla was evaluated by TUNEL assay. Besides, biochemical parameters and activities of renal antioxidant selenoenzymes [glutathione peroxidase 1 (GPx1), thioredoxin reductase (TrxR)], catalase (CAT), superoxide dismutase (SOD); concentrations of total glutathione (GSH), and malondialdehyde (MDA) levels were measured. OTA treatment was found to induce oxidative stress in rat kidney, as evidenced by marked decreases in CAT (35%) activity and GSH levels (44%) as well as increase in SOD activity (22%) vs control group. Furthermore, TUNEL analysis revealed a significant increase in the number of TUNEL-positive cells in cortex (49%) and medulla (75%) in OTA administrated group compared to control (p < 0.05). Lycopene supplementation with OTA increased GPx1 activity and GSH levels, and decreased apoptotic cell death in both cortex and medulla vs. control. The results of this study showed that at least one of the mechanisms underlying the renal toxicity of OTA is oxidative stress and apoptosis is the major form of cell death caused by OTA. Besides, our data indicate that the natural antioxidant lycopene might be partially protective against OTA-induced nephrotoxicity and oxidative stress in rat. (c) 2012 Elsevier GmbH. All rights reserved.
dc.identifier.doi10.1016/j.etp.2012.12.004
dc.identifier.endpage861
dc.identifier.issn0940-2993
dc.identifier.issn1618-1433
dc.identifier.issue6
dc.identifier.orcid0000-0003-4311-2291
dc.identifier.orcid0000-0003-3742-6841
dc.identifier.orcid0000-0001-5551-4058
dc.identifier.orcid0000-0002-6239-6114
dc.identifier.orcid0000-0002-6161-5661
dc.identifier.pmid23332503
dc.identifier.scopus2-s2.0-84880037441
dc.identifier.scopusqualityN/A
dc.identifier.startpage853
dc.identifier.urihttps://doi.org/10.1016/j.etp.2012.12.004
dc.identifier.urihttps://hdl.handle.net/11129/12766
dc.identifier.volume65
dc.identifier.wosWOS:000322929800017
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Gmbh
dc.relation.ispartofExperimental and Toxicologic Pathology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260204
dc.subjectOchratoxin A
dc.subjectOxidative stress
dc.subjectApoptosis
dc.subjectAntioxidant enzymes
dc.subjectLipid peroxidation
dc.subjectKidney
dc.titleProtective effect of lycopene against ochratoxin A induced renal oxidative stress and apoptosis in rats
dc.typeArticle

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