Comparative evaluation of hepatotoxic and nephrotoxic effects of aroclors 1221 and 1254 in female rats

dc.contributor.authorKutlu, Selim
dc.contributor.authorColakoglu, Neriman
dc.contributor.authorHalifeglu, Ihsan
dc.contributor.authorSandal, Suleyman
dc.contributor.authorSeyran, Ayse D.
dc.contributor.authorAydin, Mehmet
dc.contributor.authorYilmaz, Bayram
dc.date.accessioned2026-08-12T17:13:35Z
dc.date.issued2007
dc.departmentFırat Üniversitesi
dc.description.abstractPolychlorinated biphenyls (PCBs) are persistent environmental pollutants. This study compared effects of two PCB mixtures, Aroclors 1221 (A1221) and 1254 (A1254) on serum levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), urea, creatinine and uric acid in female rats. Histopathological changes in the liver and kidney were also examined. A group of adult Wistar rats served as controls. Groups II and III were subcutaneously injected with A 1221 and A 1254 at 10 mg/kg every other day for 6 weeks. At the end of this period, all animals were decapitated and blood samples were collected. Serum urea, creatinine, uric acid, ALT, AST and ALP levels were determined. Liver and kidney were collected for histopathological examination. They were fixed in formaldehyde and processed for light microscopy. Both A 1221 and 1254 significantly elevated serum ALT (p > 0.05) and AST (p < 0.01) levels compared to the control group. Serum ALP values were significantly increased by A1221 (p < 0.05), but they were unaffected in the A1254 group. Treatment with both A1221 and A 1254 significantly increased serum levels of urea (p < 0.05), creatinine (P < 0.01) and uric acid (except in the A 1221 group; p < 0.005). Distinct histopathological changes including renal corpuscular atrophy, peritubular vascular congestion and dilated cortical tubules, sinusoidal dilatation, congestion and mononuclear cell infiltration were observed. These findings suggest that PCBs may cause nephrotoxicity and hepatotoxicity in female rats. Copyright (c) 2005 John Wiley & Sons, Ltd.
dc.identifier.doi10.1002/cbf.1289
dc.identifier.endpage172
dc.identifier.issn0263-6484
dc.identifier.issn1099-0844
dc.identifier.issue2
dc.identifier.orcid0000-0002-2674-6535
dc.identifier.orcid0000-0003-0787-0757
dc.identifier.orcid0000-0001-9257-4797
dc.identifier.orcid0000-0001-5018-2728
dc.identifier.orcid0000-0002-4235-3942
dc.identifier.pmid16180246
dc.identifier.scopus2-s2.0-33947142916
dc.identifier.scopusqualityQ3
dc.identifier.startpage167
dc.identifier.urihttps://doi.org/10.1002/cbf.1289
dc.identifier.urihttps://hdl.handle.net/11508/51480
dc.identifier.volume25
dc.identifier.wosWOS:000244914200006
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofCell Biochemistry and Function
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectPCBs
dc.subjectALT
dc.subjectAST
dc.subjectALP
dc.subjecturea
dc.subjectcreatinine
dc.subjecturic acid
dc.titleComparative evaluation of hepatotoxic and nephrotoxic effects of aroclors 1221 and 1254 in female rats
dc.typeArticle

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