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Cited 3 time in webofscience Cited 7 time in scopus
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dc.contributor.authorHoe-Yune Jung-
dc.contributor.authorYosep Ji-
dc.contributor.authorNa-Ri Kim-
dc.contributor.authorDo-Young Kim-
dc.contributor.authorKyong-Tai Kim-
dc.contributor.authorBo-Hwa Choi-
dc.date.accessioned2017-07-19T13:20:49Z-
dc.date.available2017-07-19T13:20:49Z-
dc.date.created2017-01-23-
dc.date.issued2016-03-
dc.identifier.issn1741-427X-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/36859-
dc.description.abstractThis study investigated the antiobesity effect of an extract of the Fomitopsis pinicola Jeseng-containing formulation (FAVA), which is a combination of four natural components: Fomitopsis pinicola Jeseng; Acanthopanax senticosus; Viscum album coloratum; and Allium tuberosum. High-fat diet-(HFD-) fedmale C57BL/6J mice were treated with FAVA (200 mg/kg/day) for 12 weeks to monitor the antiobesity effect and amelioration of nonalcoholic fatty liver diseases (NAFLD). Body and white adipose tissue (WAT) weights were reduced in FAVA-treated mice, and a histological examination showed an amelioration of fatty liver in FAVA-treated mice without decreasing food consumption. Additionally, FAVA reduced serumlipid profiles, leptin, and insulin levels compared with the HFD control group. The FAVA extract suppressed lipogenic mRNA expression levels from WAT concomitantly with the cholesterol biosynthesis level in the liver. These results demonstrate the inhibitory effects of FAVA on obesity and NAFLD in the diet-induced obese (DIO) mouse model. Therefore, FAVA may be an effective therapeutic candidate for treating obesity and fatty liver caused by a high-fat diet.-
dc.languageEnglish-
dc.publisherHINDAWI PUBLISHING CORP-
dc.relation.isPartOfEVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE-
dc.titleA Fomitopsis pinicola Jeseng Formulation Has an Antiobesity Effect and Protects against Hepatic Steatosis in Mice with High-Fat Diet-Induced Obesity-
dc.typeArticle-
dc.identifier.doi10.1155/2016/7312472-
dc.type.rimsART-
dc.identifier.bibliographicCitationEVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, v.2016-
dc.identifier.wosid000375293400001-
dc.date.tcdate2018-03-23-
dc.citation.titleEVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE-
dc.citation.volume2016-
dc.contributor.affiliatedAuthorKyong-Tai Kim-
dc.identifier.scopusid2-s2.0-84971393019-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.scptc0*
dc.date.scptcdate2018-05-121*
dc.description.isOpenAccessN-
dc.type.docTypeArticle-
dc.subject.keywordPlusPPAR-GAMMA-
dc.subject.keywordPlusADIPOGENESIS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusADIPOSITY-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusSREBP-2-
dc.subject.keywordPlusLEPTIN-
dc.subject.keywordPlusENZYME-
dc.relation.journalWebOfScienceCategoryIntegrative & Complementary Medicine-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaIntegrative & Complementary Medicine-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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