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dc.contributor.authorAlemdar, Nihal Türkmen
dc.contributor.authorDemir, Selim
dc.contributor.authorYulug, Esin
dc.contributor.authorKulaber, Ali
dc.contributor.authorDemir, Elif Ayazoğlu
dc.contributor.authorErdoğan, Nadire Sevdenur
dc.contributor.authorMenteşe, Ahmet
dc.contributor.authorAliyazıcıoğlu, Yüksel
dc.date.accessioned2025-07-01T12:07:18Z
dc.date.available2025-07-01T12:07:18Z
dc.date.issued2025en_US
dc.identifier.citationAlemdar, N. T., Demir, S., Yulug, E., Kulaber, A., Demir, E. A., Erdogan, N. S., Mentese, A., & Aliyazicioglu, Y. (2025). Acetamiprid-induced testicular toxicity in mice: ameliorative effect and potential mechanisms of morin. BMC Complementary Medicine and Therapies, 25(1), 203. https://doi.org/10.1186/s12906-025-04944-5en_US
dc.identifier.issn2662-7671
dc.identifier.urihttps://doi.org/10.1186/s12906-025-04944-5
dc.identifier.urihttps://hdl.handle.net/11436/10603
dc.description.abstractBackground: Acetamiprid (ACP) is a novel chloronicotinyl insecticide that has been extensively utilized in agricultural, domestic, and public health contexts for nearly two decades. However, its potential to induce organ damage, including reproductive toxicity in mammals, has emerged as a significant concern. Morin is a naturally occurring flavonol that has gained prominence as a food supplement in recent years due to its antioxidant and anti-inflammatory properties. The objective of this study was to evaluate the protective effect of morin against testicular damage in mice subjected to ACP exposure. Methods: Thirty male Balb/c mice were randomly assigned to one of five groups, with the following treatment allocations: control, ACP (20 mg/kg), ACP + morin (15 and 30 mg/kg), and only morin (30 mg/kg). ACP and morin applications were conducted orally over a period of 14 days. Hormonal analyses were conducted on serum samples obtained from the mice, while biochemical and histological evaluations were performed on testicular samples. Results: The biochemical results demonstrated that ACP elevated oxidative stress, inflammation, and ER stress in testicular tissue by inhibiting the Nrf2 pathway, a finding that was corroborated by histopathological analyses. However, morin treatments eliminated ACP-induced Nrf2 inhibition and to activate antioxidant and anti-inflammatory mechanisms. These findings were also corroborated by the restoration of serum testosterone and inhibin B levels and the diminution of histopathological lesions. Conclusions: Overall, the findings indicated that morin may have potential protective properties against ACP-associated reproductive toxicity, however, further research is required to determine the detailed molecular mechanisms.en_US
dc.language.isoengen_US
dc.publisherSpringer Natureen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcetamipriden_US
dc.subjectER stressen_US
dc.subjectInflammationen_US
dc.subjectNrf2en_US
dc.subjectOxidative stressen_US
dc.subjectTesticular toxicityen_US
dc.titleAcetamiprid-induced testicular toxicity in mice: ameliorative effect and potential mechanisms of morinen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.contributor.institutionauthorAlemdar, Nihal Türkmen
dc.identifier.doi10.1186/s12906-025-04944-5en_US
dc.identifier.volume25en_US
dc.identifier.issue1en_US
dc.identifier.startpage203en_US
dc.relation.journalBMC Complementary Medicine and Therapiesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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