In Vitro, In Vivo, and In Silico Analysis of Pyraclostrobin and Cyprodinil and Their Mixture Reveal New Targets and Signaling Mechanisms

dc.contributor.authorKim, Yeju
dc.contributor.authorBereketoglu, Ceyhun
dc.contributor.authorSerçinoğlu, Oğlu
dc.contributor.authorPradhan, Ajay
dc.date.accessioned2025-10-29T11:20:47Z
dc.date.issued2024
dc.departmentFakülteler, Mühendislik Fakültesi, Biyomühendislik Bölümü
dc.description.abstractPyraclostrobin and cyprodinil are broad-spectrum fungicides that are used in crops to control diseases. However, they are excessively used and, as a result, end up in the environment and threaten human health and ecosystems. Hence, knowledge of their mechanisms of action is critical to revealing their environmental fate and negative effects and regulating their use. In the present study, we conducted a comprehensive study to show the adverse effects of pyraclostrobin, cyprodinil, and their mixture using zebrafish larvae and different cell lines. Several end points were investigated, including mortality, development, gene expression, reporter assays, and molecular docking simulations. We found that both compounds and their mixture caused developmental delays and mortality in zebrafish, with a higher effect displayed by pyraclostrobin. Both compounds altered the expression of genes involved in several signaling pathways, including oxidative stress and mitochondrial function, lipid and drug metabolisms, the cell cycle, DNA damage, apoptosis, and inflammation. A noteworthy result of this study is that cyprodinil and the mixture group acted as NF kappa B activators, while pyraclostrobin demonstrated antagonist activity. The AHR activity was also upregulated by cyprodinil and the mixture group; however, pyraclostrobin did not show any effect. For the first time, we also demonstrated that pyraclostrobin had androgen receptor antagonist activity.
dc.description.sponsorshipKnowledge Foundation
dc.description.sponsorshipMarmara University
dc.description.sponsorshipWe would like to thank Orebro University and Marmara University for supporting this study.
dc.identifier.doi10.1021/acs.chemrestox.3c00371
dc.identifier.endpage512
dc.identifier.issn0893-228X
dc.identifier.issn1520-5010
dc.identifier.issue3
dc.identifier.orcid0000-0001-9400-7892
dc.identifier.orcid0000-0003-1361-8160
dc.identifier.pmid38419406
dc.identifier.scopus2-s2.0-85186426642
dc.identifier.scopusqualityQ1
dc.identifier.startpage497
dc.identifier.urihttps://doi.org/10.1021/acs.chemrestox.3c00371
dc.identifier.urihttps://hdl.handle.net/20.500.14854/8732
dc.identifier.volume37
dc.identifier.wosWOS:001176392800001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAmer Chemical Soc
dc.relation.ispartofChemical Research in Toxicology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectAryl-Hydrocarbon Receptor
dc.subjectNf-Kappa-B
dc.subjectAndrogen Receptor
dc.subjectMitochondrial Dysfunction
dc.subjectOxidative Stress
dc.subjectZebrafish
dc.subjectPesticides
dc.subjectToxicity
dc.subjectFungicides
dc.subjectWater
dc.titleIn Vitro, In Vivo, and In Silico Analysis of Pyraclostrobin and Cyprodinil and Their Mixture Reveal New Targets and Signaling Mechanisms
dc.typeArticle

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