Quercetin prevents docetaxel- induced testicular damage in rats

dc.contributor.authorAltintas, R.
dc.contributor.authorCiftci, O.
dc.contributor.authorAydin, M.
dc.contributor.authorAkpolat, N.
dc.contributor.authorOguz, F.
dc.contributor.authorBeytur, A.
dc.date.accessioned2026-08-12T17:16:27Z
dc.date.issued2015
dc.departmentFırat Üniversitesi
dc.description.abstractThe protective effect of quercetin on docetaxel - an anticancer agent - induced testicular damage in rats was investigated. Thirty-two rats were randomly divided into four groups: group 1 - control, carrier solutions were given; group 2 - quarcetin 20mgkg(-1)day(-1) was given orally; group 3 - docetaxel 5mgkg(-1) was given intraperitoneally as single dose; group 4 - docetaxel and quarcetin were given together. The histopathological changes; the specific biochemical markers, including antioxidants; and the sperm characteristics were evaluated. Docetaxel caused a significant increase in TBARS level and a significant decrease in SOD, GPX, CAT and GSH levels in the testicular tissues compared with the control group, whereas quercetin led to a significant decrease in lipid peroxidation, which was caused by docetaxel, via reducing TBARS level and increasing the levels of SOD, CAT, GPX and GSH. In addition, after docetaxel administration, sperm motility, sperm concentration, testicular and epididymis weights were significantly decreased and abnormal sperm rate and histopathological changes were increased. However, these effects of docetaxel on sperm parameters, histological changes and the tissue weights were eliminated by quercetin treatment. Our results show that the administration of docetaxel induced the testicular damage (oxidative stress, testes tissue damage and sperm parameters), and quercetin prevented docetaxel-induced testicular damage in rats.
dc.description.sponsorshipInonu University, Scientific Research Projects Coordination Unit [2011/195]
dc.description.sponsorshipThis study has been supported by Inonu University, Scientific Research Projects Coordination Unit (Project No: 2011/195).
dc.identifier.doi10.1111/and.12253
dc.identifier.endpage256
dc.identifier.issn0303-4569
dc.identifier.issn1439-0272
dc.identifier.issue3
dc.identifier.orcid0000-0001-5755-3560
dc.identifier.orcid0000-0002-9138-2117
dc.identifier.orcid0000-0003-3145-3005
dc.identifier.orcid0000-0002-6494-9229
dc.identifier.pmid24601972
dc.identifier.scopus2-s2.0-84923636571
dc.identifier.scopusqualityQ1
dc.identifier.startpage248
dc.identifier.urihttps://doi.org/10.1111/and.12253
dc.identifier.urihttps://hdl.handle.net/11508/52291
dc.identifier.volume47
dc.identifier.wosWOS:000350490000003
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofAndrologia
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectDocetaxel
dc.subjectquercetin
dc.subjectrat
dc.subjecttesticular damage
dc.titleQuercetin prevents docetaxel- induced testicular damage in rats
dc.typeArticle

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