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Integrative assessment of biomarker responses in pale chub (Zacco platypus) exposed to copper and benzo[a]pyrene

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dc.contributor.authorKim, Woo-Keun-
dc.contributor.authorLee, Sung-Kyu-
dc.contributor.authorChoi, Kyungho-
dc.contributor.authorJung, Jinho-
dc.date.accessioned2021-09-06T00:45:35Z-
dc.date.available2021-09-06T00:45:35Z-
dc.date.created2021-06-14-
dc.date.issued2013-06-01-
dc.identifier.issn0147-6513-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/103003-
dc.description.abstractMulti-level biomarker responses (molecular/biochemical and histological/physiological levels) were studied to assess the sublethal toxicities of copper (Cu: 1.25, 5, and 20 mu g/L) and benzo[a]pyrene (BaP: 0.5, 5, and 50 mu g/L) induced in the freshwater pale chub Zacco platypus. Except for the kidney tissues when exposed to 20 mu g Cu/L, no significant differences were observed at the histological or physiological levels among the treatment groups. However, various molecular and biochemical responses were observed in Z. platypus, and these responses primarily depended on exposure time. Upon Cu exposure, both DNA single-strand breaks (COMET) and metallothionein (MT) concentration significantly increased after 4 days, whereas there were no significant changes after 14 days of exposure. Both 4 and 14 days of BaP exposure induced significant increases in COMET and 7-ethoxyresorufin-O-deethylase (EROD) activity, but there was no significant difference between them. Additionally, both Cu and BaP induced acetylcholinesterase (AChE) activity only after 14 days of exposure. The current findings demonstrate that the differences in the responses of MT and EROD are associated with each chemical's particular mode of action. Biomarker responses at the molecular and biochemical levels were quantized in terms of the integrated biomarker response (IBR) index to compare the toxicities of Cu and BaP. The IBR values were well correlated with the concentrations of Cu and BaP, and the correlations were enhanced at 4 days of exposure (r(2) = 0.849 and 0.945, respectively) compared with 14 days (r(2) = 0.412 and 0.634, respectively). These results suggest that the IBR index may be a useful tool for the integrative quantification of the molecular and biochemical biomarker responses in a short-term exposure to Cu and BaP. (c) 2013 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectCYPRINUS-CARPIO-
dc.subjectRISK-ASSESSMENT-
dc.subjectCOMMON CARP-
dc.subjectMYTILUS-GALLOPROVINCIALIS-
dc.subjectOXIDATIVE STRESS-
dc.subjectJAPANESE MEDAKA-
dc.subjectRAINBOW-TROUT-
dc.subjectCOMET ASSAY-
dc.subjectUSEFUL TOOL-
dc.subjectDNA-DAMAGE-
dc.titleIntegrative assessment of biomarker responses in pale chub (Zacco platypus) exposed to copper and benzo[a]pyrene-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Jinho-
dc.identifier.doi10.1016/j.ecoenv.2013.02.010-
dc.identifier.scopusid2-s2.0-84876990996-
dc.identifier.wosid000319030700010-
dc.identifier.bibliographicCitationECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, v.92, pp.71 - 78-
dc.relation.isPartOfECOTOXICOLOGY AND ENVIRONMENTAL SAFETY-
dc.citation.titleECOTOXICOLOGY AND ENVIRONMENTAL SAFETY-
dc.citation.volume92-
dc.citation.startPage71-
dc.citation.endPage78-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusCYPRINUS-CARPIO-
dc.subject.keywordPlusRISK-ASSESSMENT-
dc.subject.keywordPlusCOMMON CARP-
dc.subject.keywordPlusMYTILUS-GALLOPROVINCIALIS-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusJAPANESE MEDAKA-
dc.subject.keywordPlusRAINBOW-TROUT-
dc.subject.keywordPlusCOMET ASSAY-
dc.subject.keywordPlusUSEFUL TOOL-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordAuthorBiochemical endpoint-
dc.subject.keywordAuthorHistological endpoint-
dc.subject.keywordAuthorIntegrated biomarker response-
dc.subject.keywordAuthorMolecular biomarker-
dc.subject.keywordAuthorPhysiological endpoint-
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