Naringenin Attenuates Testicular Toxicity and Apoptosis in Rats Chronically Exposed to Mercury Chloride

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Özet

Mercury is an industrial toxin with detrimental effects on the reproductive system. This study explored the impact of naringenin (NAR) on testicular toxicity and apoptosis in rats chronically exposed to mercury chloride (MC). The research involved 41 adult male Wistar-Albino rats aged about 2.5 months, which were allocated into 5 groups: group 1 was a control group, group 2 received 100mg/kg of NAR, group 3 was exposed to MC, group 4 received both MC and 50mg/kg of NAR, and group 5 received both MC and 100mg/kg of NAR. For the treatments, the control group took 1mL/kg saline via intraperitoneal (ip) injection and 1mL/kg corn oil via gavage. MC was administered at 0.4mg/kg/day to the MC groups via ip, and NAR was delivered in corn oil at 50 and 100mg/kg/day to the respective NAR groups via gavage. All treatments were performed over a period of 20 days, with MC administration starting 1 hour after NAR administration. The irregularity and loss in spermatogenic cell organization, degeneration and vacuolization in tubules, edema, and congestion in interstitial areas of the testicular tissue of the MC group were alleviated by NAR administration. In addition, the increase in Caspase 3, iNOS, and eNOS immunoreactivities of the MC group were alleviated by NAR administration. In conclusion, it was found that NAR had protective and therapeutic effects against oxidative damage, histopathological changes, apoptosis, and altered spermatological parameters resulting from MC exposure in the testis, and 100mg/kg NAR provided positive effects on altered histopathological analysis, spermatological parameters, and apoptosis.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/1583Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.29261/pakvetj/2025.196Yayıncı resmi DOI adresi
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorKahramanoğullari, Merve
dc.contributor.authorErişir, Mine
dc.contributor.authorYaman, Mine
dc.contributor.authorKaya, Şeyma Özer
dc.contributor.authorAk, Tuba Parlak
dc.date.accessioned2026-10-28T14:54:21.922159512Z
dc.date.available2026-10-28T14:54:21.922159512Z
dc.date.issued2025
dc.description.abstractMercury is an industrial toxin with detrimental effects on the reproductive system. This study explored the impact of naringenin (NAR) on testicular toxicity and apoptosis in rats chronically exposed to mercury chloride (MC). The research involved 41 adult male Wistar-Albino rats aged about 2.5 months, which were allocated into 5 groups: group 1 was a control group, group 2 received 100mg/kg of NAR, group 3 was exposed to MC, group 4 received both MC and 50mg/kg of NAR, and group 5 received both MC and 100mg/kg of NAR. For the treatments, the control group took 1mL/kg saline via intraperitoneal (ip) injection and 1mL/kg corn oil via gavage. MC was administered at 0.4mg/kg/day to the MC groups via ip, and NAR was delivered in corn oil at 50 and 100mg/kg/day to the respective NAR groups via gavage. All treatments were performed over a period of 20 days, with MC administration starting 1 hour after NAR administration. The irregularity and loss in spermatogenic cell organization, degeneration and vacuolization in tubules, edema, and congestion in interstitial areas of the testicular tissue of the MC group were alleviated by NAR administration. In addition, the increase in Caspase 3, iNOS, and eNOS immunoreactivities of the MC group were alleviated by NAR administration. In conclusion, it was found that NAR had protective and therapeutic effects against oxidative damage, histopathological changes, apoptosis, and altered spermatological parameters resulting from MC exposure in the testis, and 100mg/kg NAR provided positive effects on altered histopathological analysis, spermatological parameters, and apoptosis.
dc.description.sponsorshipFirat University Scientific Research Projects Management Unit, FUBAP, (VF.21.21)
dc.description.sponsorshipFirat University Scientific Research Projects Management Unit, FUBAP
dc.identifier.doi10.29261/pakvetj/2025.196
dc.identifier.eissn2074-7764
dc.identifier.endpage798
dc.identifier.issn0253-8318
dc.identifier.issue2
dc.identifier.scopus2-s2.0-105010873106
dc.identifier.startpage791
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/1583
dc.identifier.volume45
dc.identifier.wosWOS:001551221300029
dc.language.isoen
dc.publisherUniversity of Agriculture
dc.relation.ispartofPakistan Veterinary Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectApoptosis
dc.subjectMercury (II) Chloride
dc.subjectNaringenin
dc.subjectOxidative Damage
dc.subjectReproductive Toxicity
dc.subject.classificationVeterinary Sciences
dc.subject.othercaspase 3
dc.subject.othercatalase
dc.subject.otherglutathione
dc.subject.otherglutathione peroxidase
dc.subject.othermalonaldehyde
dc.subject.othermercury chloride
dc.subject.othernaringenin
dc.subject.othersuperoxide dismutase
dc.subject.otheradult
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otherapoptosis
dc.subject.otherArticle
dc.subject.othercontrolled study
dc.subject.otherDNA damage
dc.subject.otherDNA fragmentation
dc.subject.otherhistology
dc.subject.otherlipid peroxidation
dc.subject.othermale
dc.subject.othernonhuman
dc.subject.otheroxidative stress
dc.subject.otherrat
dc.subject.othersemen analysis
dc.subject.othersperm quality
dc.subject.otherspermatocyte
dc.subject.otherspermatogenesis
dc.subject.otherspermatozoon motility
dc.subject.otherTesticular Toxicity
dc.subject.othertestis tissue
dc.subject.othertoxicity
dc.titleNaringenin Attenuates Testicular Toxicity and Apoptosis in Rats Chronically Exposed to Mercury Chloride
dc.typeArticle
rdl.citation.openalex0
rdl.citation.scopus1
rdl.citation.wos1
rdl.oa.statusclosed
rdl.scopus.quartileQ1
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)