Chrysin and flunixin meglumine mitigate overloaded copper-induced testicular and spermatological damages via modulation of oxidative stress and apoptosis in rats

dc.contributor.authorParlak, Tuba
dc.contributor.authorSeven, Pinar Tatli
dc.contributor.authorGur, Seyfettin
dc.contributor.authorGul, Burcu
dc.contributor.authorYaman, Mine
dc.contributor.authorSeven, Ismail
dc.date.accessioned2026-08-12T17:19:57Z
dc.date.issued2022
dc.departmentFırat Üniversitesi
dc.description.abstractThis study aimed to evaluate the possible protective actions of chrysin and flunixine meglumine on testicular and spermatological injuries experimentally stimulated by copper. We separated 36 male Sprague-Dawley rats into six equal groups: control, chrysin, flunixine meglumine, copper, copper +chrysin and copper +flunixine meglumine. Chrysin (50 mg/kg/bw/po), flunixine meglumine (2.2 mg/kg/bw/ip) and copper (500 mg/kg/bw/po) were administered day to day for 21 days. Copper administration caused significant morphological, physiological and biochemical alterations compared to the control group, which are as follows: production of oxidative stress, thanks to rise in testis lipid peroxidation and fall in antioxidant enzyme concentrations, decrease in sperm quality and increase in morphologic sperm abnormalities, suppression of spermatogenesis and prominent alterations in the testis histomorphology and induction of apoptosis in the testis tissues. On the other hand, compared to the copper group, treatment with chrysin or flunixine meglumine significantly attenuated these alterations. In conclusion, chrysin and flunixine meglumine have benefits such as antioxidant, antiapoptotic and anti-inflammatory against copper-induced testicular and spermatological damages in rats via the modulation of oxidative stress and apoptosis. Consequently, chrysin is a natural product which has comparable therapeutic actions to flunixine meglumine on the male reproductive system.
dc.description.sponsorshipFirat University Scientific Research Projects Unit, Elazig, Turkey [VF.14.11]
dc.description.sponsorshipThe present research was funded by Firat University Scientific Research Projects Unit, Elazig, Turkey (VF.14.11).
dc.identifier.doi10.1111/and.14327
dc.identifier.issn0303-4569
dc.identifier.issn1439-0272
dc.identifier.issue2
dc.identifier.orcid0000-0002-8318-7995
dc.identifier.orcid0000-0002-9122-8953
dc.identifier.orcid0000-0002-0067-4190
dc.identifier.pmid34817900
dc.identifier.scopus2-s2.0-85119701633
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1111/and.14327
dc.identifier.urihttps://hdl.handle.net/11508/53370
dc.identifier.volume54
dc.identifier.wosWOS:000721824000001
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.subjectapoptosis
dc.subjectchrysin
dc.subjectcopper
dc.subjectflunixin meglumine
dc.subjectreproductive toxicity
dc.titleChrysin and flunixin meglumine mitigate overloaded copper-induced testicular and spermatological damages via modulation of oxidative stress and apoptosis in rats
dc.typeArticle

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