The Protective Effect of ENA Actimineral Resource A on CCl4-Induced Liver Injury in Rats

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dc.contributor.authorHong, Il-Hwako
dc.contributor.authorJi, Hoonko
dc.contributor.authorHwa, Sung-Yongko
dc.contributor.authorJeong, Won-ilko
dc.contributor.authorJeong, Da-Heeko
dc.contributor.authorDo, Sun-Heeko
dc.contributor.authorKim, Ji-Minko
dc.contributor.authorKi, Mi-Ranko
dc.contributor.authorPark, Jin-Kyuko
dc.contributor.authorGoo, Moon-Jungko
dc.contributor.authorHwang, Ok-Kyungko
dc.contributor.authorHong, Kyung-Sookko
dc.contributor.authorHan, Jung-Younko
dc.contributor.authorChung, Hae-Youngko
dc.contributor.authorJeong, Kyu-Shikko
dc.date.accessioned2013-03-12T05:31:05Z-
dc.date.available2013-03-12T05:31:05Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2011-06-
dc.identifier.citationMARINE BIOTECHNOLOGY, v.13, no.3, pp.462 - 473-
dc.identifier.issn1436-2228-
dc.identifier.urihttp://hdl.handle.net/10203/101451-
dc.description.abstractENA Actimineral Resource A (ENA-A) is alkaline water that is composed of refined edible cuttlefish bone and two different species of seaweed, Phymatolithon calcareum and Lithothamnion corallioides. In the present study, ENA-A was investigated as an antioxidant to protect against CCl4-induced oxidative stress and hepatotoxicity in rats. Liver injury was induced by either subacute or chronic CCl4 administration, and the rats had free access to tap water mixed with 0% (control group) or 10% (v/v) ENA-A for 5 or 8 weeks. The results of histological examination and measurement of antioxidant activity showed that the reactive oxygen species production, lipid peroxidation, induction of CYP2E1 were decreased and the antioxidant activity, including glutathione and catalase production, was increased in the ENA-A groups as compared with the control group. On 2-DE gel analysis of the proteomes, 13 differentially expressed proteins were obtained in the ENA-A groups as compared with the control group. Antioxidant proteins, including glutathione S-transferase, kelch-like ECH-associated protein 1, and peroxiredoxin 1, were increased with hepatocyte nuclear factor 3-beta and serum albumin precursor, and kininogen precursor decreased more in the ENA-A groups than compared to the control group. In conclusion, our results suggest that ENA-A does indeed have some protective capabilities against CCl4-induced liver injury through its antioxidant function.-
dc.languageEnglish-
dc.publisherSPRINGER-
dc.subjectCARBON-TETRACHLORIDE-
dc.subjectGENE-EXPRESSION-
dc.subjectIN-VIVO-
dc.subjectLIPID-PEROXIDATION-
dc.subjectOXIDATIVE STRESS-
dc.subjectENZYMES-
dc.subjectMETABOLISM-
dc.subjectKININOGEN-
dc.subjectPHASE-
dc.subjectNRF2-
dc.titleThe Protective Effect of ENA Actimineral Resource A on CCl4-Induced Liver Injury in Rats-
dc.typeArticle-
dc.identifier.wosid000291168500012-
dc.identifier.scopusid2-s2.0-79957980389-
dc.type.rimsART-
dc.citation.volume13-
dc.citation.issue3-
dc.citation.beginningpage462-
dc.citation.endingpage473-
dc.citation.publicationnameMARINE BIOTECHNOLOGY-
dc.identifier.doi10.1007/s10126-010-9317-8-
dc.contributor.localauthorJeong, Won-il-
dc.contributor.nonIdAuthorHong, Il-Hwa-
dc.contributor.nonIdAuthorJi, Hoon-
dc.contributor.nonIdAuthorHwa, Sung-Yong-
dc.contributor.nonIdAuthorJeong, Da-Hee-
dc.contributor.nonIdAuthorDo, Sun-Hee-
dc.contributor.nonIdAuthorKim, Ji-Min-
dc.contributor.nonIdAuthorKi, Mi-Ran-
dc.contributor.nonIdAuthorPark, Jin-Kyu-
dc.contributor.nonIdAuthorGoo, Moon-Jung-
dc.contributor.nonIdAuthorHwang, Ok-Kyung-
dc.contributor.nonIdAuthorHong, Kyung-Sook-
dc.contributor.nonIdAuthorHan, Jung-Youn-
dc.contributor.nonIdAuthorChung, Hae-Young-
dc.contributor.nonIdAuthorJeong, Kyu-Shik-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorENA actimineral resource A-
dc.subject.keywordAuthorAntioxidant capability-
dc.subject.keywordAuthorHepatoxicity-
dc.subject.keywordAuthorSeaweed-
dc.subject.keywordAuthorCarbon tetrachloride-
dc.subject.keywordPlusCARBON-TETRACHLORIDE-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusKININOGEN-
dc.subject.keywordPlusPHASE-
dc.subject.keywordPlusNRF2-
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