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Endocrine disruption and consequences of chronic exposure to ibuprofen in Japanese medaka (Oryzias latipes) and freshwater cladocerans Daphnia magna and Moina macrocopa

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dc.contributor.authorHan, Sunyoung-
dc.contributor.authorChoi, Kyungho-
dc.contributor.authorKim, Jungkon-
dc.contributor.authorJi, Kyunghee-
dc.contributor.authorKim, Sunmi-
dc.contributor.authorAhn, Byeongwoo-
dc.contributor.authorYun, Junheon-
dc.contributor.authorChoi, Kyunghee-
dc.contributor.authorKhim, Jong Seong-
dc.contributor.authorZhang, Xiaowei-
dc.contributor.authorGiesy, John P.-
dc.date.accessioned2021-09-08T01:35:54Z-
dc.date.available2021-09-08T01:35:54Z-
dc.date.created2021-06-11-
dc.date.issued2010-07-01-
dc.identifier.issn0166-445X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/116081-
dc.description.abstractDespite frequent detection of ibuprofen in aquatic environments, the hazards associated with long-term exposure to ibuprofen have seldom been investigated. Ibuprofen is suspected of influencing sex steroid hormones through steroidogenic pathways in both vertebrates and invertebrates. In this study, the effect of ibuprofen on sex hormone balance and the associated mechanisms was investigated in vitro by use of H295R cells. We also conducted chronic toxicity tests using freshwater fish, Oryzias latipes, and two freshwater cladocerans. Daphnia magna and Moina macrocopa, for up to 144 and 21 d of exposure, respectively. Ibuprofen exposure increased 17 beta-estradiol (E2) production and aromatase activity in H295R cells. Testosterone (T) production decreased in a dose-dependent manner. For D. magna, the 48 h immobilization EC50 was 51.4 mg/L and the 21 d reproduction NOEC was <1.23 mg/L; for M. macrocopa, the 48 h immobilization EC50 was 72.6 mg/L and the 7 d reproduction NOEC was 25 mg/L For O.latipes, 120 d survival NOEC was 0.0001 mg/L In addition, ibuprofen affected several endpoints related to reproduction of the fish, including induction of vitellogenin in male fish, fewer broods per pair, and more eggs per brood. Parental exposure to as low as 0.0001 mg/L ibuprofen delayed hatching of eggs even when they were transferred to and cultured in clean water. Delayed hatching is environmentally relevant because this may increase the risk of being predated. For O. latipes, the acute-to-chronic ratio of ibuprofen was estimated to be greater than 1000. Overall, relatively high acute-to-chronic ratio and observation of reproduction damage in medaka fish at environmentally relevant ranges of ibuprofen warrant the need for further studies to elucidate potential ecological consequences of ibuprofen contamination in the aquatic environment. (C) 2010 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.subjectHAZARD ASSESSMENT-
dc.subjectCHRONIC TOXICITY-
dc.subjectSURFACE-WATER-
dc.subjectH295R CELLS-
dc.subjectPHARMACEUTICALS-
dc.subjectDRUGS-
dc.subjectCNIDARIAN-
dc.subjectHISTORY-
dc.subjectRISK-
dc.titleEndocrine disruption and consequences of chronic exposure to ibuprofen in Japanese medaka (Oryzias latipes) and freshwater cladocerans Daphnia magna and Moina macrocopa-
dc.typeArticle-
dc.contributor.affiliatedAuthorKhim, Jong Seong-
dc.identifier.doi10.1016/j.aquatox.2010.02.013-
dc.identifier.scopusid2-s2.0-77953687759-
dc.identifier.wosid000279061800005-
dc.identifier.bibliographicCitationAQUATIC TOXICOLOGY, v.98, no.3, pp.256 - 264-
dc.relation.isPartOfAQUATIC TOXICOLOGY-
dc.citation.titleAQUATIC TOXICOLOGY-
dc.citation.volume98-
dc.citation.number3-
dc.citation.startPage256-
dc.citation.endPage264-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMarine & Freshwater Biology-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryMarine & Freshwater Biology-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusHAZARD ASSESSMENT-
dc.subject.keywordPlusCHRONIC TOXICITY-
dc.subject.keywordPlusSURFACE-WATER-
dc.subject.keywordPlusH295R CELLS-
dc.subject.keywordPlusPHARMACEUTICALS-
dc.subject.keywordPlusDRUGS-
dc.subject.keywordPlusCNIDARIAN-
dc.subject.keywordPlusHISTORY-
dc.subject.keywordPlusRISK-
dc.subject.keywordAuthorNon-steroidal anti-inflammatory drug-
dc.subject.keywordAuthorFish-
dc.subject.keywordAuthorSteroidogenesis-
dc.subject.keywordAuthorH295R cell-
dc.subject.keywordAuthorAromatase-
dc.subject.keywordAuthorHormones-
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