Publication:
Examination of Caspase-Dependent Apoptotic and Necrotic Changes in Rat Kidney Exposed to Different Doses of Permethrin

dc.authorscopusid16238460900
dc.authorscopusid23093995200
dc.authorscopusid36058260100
dc.authorscopusid16237906700
dc.authorscopusid56353804300
dc.contributor.authorGüvenç, D.
dc.contributor.authorKabak, Y.B.
dc.contributor.authorAtmaca, E.
dc.contributor.authorAksoy, A.
dc.contributor.authorGüvenç, T.
dc.date.accessioned2020-06-21T14:06:46Z
dc.date.available2020-06-21T14:06:46Z
dc.date.issued2013
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Güvenç] Dilek, , Department of Pharmacology and Toxicology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kabak] Yonca Betil, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Atmaca] Enes,; [Aksoy] Abdurrahman,; [Güvenç] Tolga, Department of Pathology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractWe investigated dose-related pathological alterations and apoptosis in rat kidney tissue exposed to permethrin. Histopathological findings, apoptotic cell death and urinary 3-phenoxybenzoic acid concentrations (3-PBA) were evaluated. Different doses of permethrin were administered to animals by oro-gastric gavage. A dose-dependent increase of urine 3-PBA concentration was observed in all the permethrin-treated groups. SDS-PAGE separated 30-45 kD and 100-220 kD protein bands in all experimental groups. Histopathologically, degenerative changes were observed in the epithelial lining of the S1, S2, and S3 segments of the renal proximal tubules. Apoptotic cells were seen in the inner stripe of the outer medulla in Group I, and both the cortex and medulla in Groups II and III. Immunohistochemical staining of caspase 3 and caspase 9 also was observed in the same areas. Our results suggest that damage to regions of the proximal tubules is dose-related, and caspase-9-dependent, mitochondria-related apoptotic cell death could play an important role in permethrin-induced nephrotoxicity. We also observed morphologically necrotic cells. We concluded that both necrosis and apoptosis are produced by permethrin. © 2013 The Biological Stain Commission.en_US
dc.identifier.doi10.3109/10520295.2012.736637
dc.identifier.endpage85en_US
dc.identifier.issn1052-0295
dc.identifier.issn1473-7760
dc.identifier.issue2en_US
dc.identifier.pmid23167626
dc.identifier.scopus2-s2.0-84872298137
dc.identifier.scopusqualityQ3
dc.identifier.startpage76en_US
dc.identifier.urihttps://doi.org/10.3109/10520295.2012.736637
dc.identifier.volume88en_US
dc.identifier.wosWOS:000321903600002
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherTaylor & Francis Ltden_US
dc.relation.ispartofBiotechnic & Histochemistryen_US
dc.relation.journalBiotechnic & Histochemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject3-Phenoxybenzoic Aciden_US
dc.subjectCaspaseen_US
dc.subjectImmunohistochemistryen_US
dc.subjectPermethrinen_US
dc.subjectTUNELen_US
dc.subjectUrine Proteinsen_US
dc.titleExamination of Caspase-Dependent Apoptotic and Necrotic Changes in Rat Kidney Exposed to Different Doses of Permethrinen_US
dc.typeArticleen_US
dspace.entity.typePublication

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