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

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Özet

This 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.

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https://doi.org/10.1111/and.14327Yayıncı resmi DOI adresi
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AlanDeğerDil
dc.contributor.authorParlak Ak, Tuba
dc.contributor.authorTatli Seven, Pinar
dc.contributor.authorGur, Seyfettin
dc.contributor.authorGul, Burcu
dc.contributor.authorYaman, Mine
dc.contributor.authorSeven, Ismail
dc.date.accessioned2026-10-28T14:56:04.752294358Z
dc.date.available2026-10-28T14:56:04.752294358Z
dc.date.issued2022
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.sponsorshipCrimson Interactive Inc.
dc.description.sponsorshipFirat University Scientific Research Projects Management Unit, FÜBAP
dc.identifier.articlenumbere14327
dc.identifier.doi10.1111/and.14327
dc.identifier.issn0303-4569
dc.identifier.issue2
dc.identifier.pmid34817900
dc.identifier.scopus2-s2.0-85119701633
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/2991
dc.identifier.volume54
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofAndrologia
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectapoptosis
dc.subjectchrysin
dc.subjectcopper
dc.subjectflunixin meglumine
dc.subjectreproductive toxicity
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherApoptosis
dc.subject.otherClonixin
dc.subject.otherCopper
dc.subject.otherFlavonoids
dc.subject.otherMale
dc.subject.otherOxidative Stress
dc.subject.otherRats
dc.subject.otherRats, Sprague-Dawley
dc.subject.otherSpermatozoa
dc.subject.otherTestis
dc.subject.otherantioxidant
dc.subject.otherchrysin
dc.subject.otherflunixin meglumine
dc.subject.othernatural product
dc.subject.otherflavonoid
dc.subject.otheranimal experiment
dc.subject.otherArticle
dc.subject.othercontrolled study
dc.subject.otherdata analysis software
dc.subject.otherenzyme activity
dc.subject.othergroup therapy
dc.subject.otherhistology
dc.subject.otherhistopathology
dc.subject.otherinjury
dc.subject.otherlipid peroxidation
dc.subject.othernonhuman
dc.subject.otherrat
dc.subject.otherreproductive toxicity
dc.subject.othersemen abnormality
dc.subject.othersemen parameters
dc.subject.othersperm quality
dc.subject.otherspermatogenesis
dc.subject.otherSprague Dawley rat
dc.subject.othertestis tissue
dc.subject.otheranimal
dc.subject.othermetabolism
dc.subject.otherspermatozoon
dc.titleChrysin and flunixin meglumine mitigate overloaded copper-induced testicular and spermatological damages via modulation of oxidative stress and apoptosis in rats
dc.typeArticle
rdl.citation.openalex4
rdl.citation.scopus4
rdl.oa.statusgreen
rdl.oa.urlhttps://hdl.handle.net/11508/53370
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS