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The adverse effects of selenomethionine on skeletal muscle, liver, and brain in the steelhead trout (Oncorhynchus mykiss)

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dc.contributor.authorLee, Jang-Won-
dc.contributor.authorDeng, Dong-Fang-
dc.contributor.authorLee, Jinsu-
dc.contributor.authorKim, Kiyoung-
dc.contributor.authorJung, Hyun Jin-
dc.contributor.authorChoe, Youngshik-
dc.contributor.authorPark, Seung Hwa-
dc.contributor.authorYoon, Minjung-
dc.date.accessioned2023-08-16T09:43:37Z-
dc.date.available2023-08-16T09:43:37Z-
dc.date.created2022-01-11-
dc.date.issued2020-11-
dc.identifier.issn1382-6689-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/568-
dc.description.abstractJuvenile Oncorhynchus mykiss (average weight 22.3 g) were fed one of five selenomethionine diets (1.09, 8.79, 15.37, 30.79, or 61.58 mg Se/kg diet). After 4 weeks, hepatic catalase activity over 15.37 mg Se/kg diets was significantly decreased, and the glutathione peroxidase activity over 30.79 mg Se/kg diets was elevated compared to the controls. In the brain, the dopamine levels at 61.58 mg Se/kg diet and the serotonin levels over 15.37 mg Se/kg diets were significantly increased, whereas the 3,4-dihydroxyphenylacetic acid, homovanillic acid, and dopamine turnover, and the 5-hydroxyindoleacetic acid and serotonin turnover over 30.79 mg Se/kg diets were decreased. In muscle, the 3-nitrotyrosine level over 15.37 mg Se/kg diets, acetylcholine esterase activity over 30.79 mg Se/kg diets, and histological alterations over 8.79 mg Se/kg diets were increased. Our current results showed that selenomethionine disrupted dopamine and serotonin metabolism in the brain and damaged the neuromuscular system in skeletal muscle.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER-
dc.titleThe adverse effects of selenomethionine on skeletal muscle, liver, and brain in the steelhead trout (Oncorhynchus mykiss)-
dc.typeArticle-
dc.contributor.affiliatedAuthorJung, Hyun Jin-
dc.contributor.affiliatedAuthorChoe, Youngshik-
dc.identifier.doi10.1016/j.etap.2020.103451-
dc.identifier.scopusid2-s2.0-85087206837-
dc.identifier.wosid000583776900010-
dc.identifier.bibliographicCitationENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, v.80-
dc.relation.isPartOfENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY-
dc.citation.titleENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY-
dc.citation.volume80-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusDIETARY SELENOMETHIONINE-
dc.subject.keywordPlusHETEROCYCLIC AMINES-
dc.subject.keywordPlusCHRONIC EXPOSURE-
dc.subject.keywordPlusSODIUM SELENITE-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusACETYLCHOLINESTERASE-
dc.subject.keywordPlusNEUROTOXICITY-
dc.subject.keywordPlusANTIOXIDANT-
dc.subject.keywordAuthorSelenium neurotoxicity-
dc.subject.keywordAuthorSteelhead trout-
dc.subject.keywordAuthorNeuromuscular system-
dc.subject.keywordAuthorHistopathology-
dc.subject.keywordAuthorOxidative stress-
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