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Semen Cuscutae Administration Improves Hepatic Lipid Metabolism and Adiposity in High Fat Diet-Induced Obese Mice

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dc.contributor.authorMoon, Jiyoung-
dc.contributor.authorHa, Min Jin-
dc.contributor.authorShin, Min-Jeong-
dc.contributor.authorKim, Oh Yoen-
dc.contributor.authorYoo, Eun Hye-
dc.contributor.authorSong, Juhyun-
dc.contributor.authorChung, Ji Hyung-
dc.date.accessioned2021-08-31T22:53:43Z-
dc.date.available2021-08-31T22:53:43Z-
dc.date.created2021-06-18-
dc.date.issued2019-12-
dc.identifier.issn2072-6643-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/61482-
dc.description.abstractSince arginase has been shown to compete with nitric oxide (NO) synthase, emerging evidence has reported that arginase inhibition improves obesity by increasing NO production. Semen cuscutae (SC), which is a well-known Chinese medicine, has multiple biological functions such as anti-oxidant function and immune regulation. In this study, we investigated whether the SC as a natural arginase inhibitor influences hepatic lipid abnormalities and whole-body adiposity in high-fat diet (HFD)-induced obese mice. The lipid accumulation was significantly reduced by SC treatment in oleic acid -induced hepatic steatosis in vitro. Additionally, SC supplementation substantially lowered HFD-induced increases in arginase activity and weights of liver and visceral fat tissue, while increasing hepatic NO. Furthermore, elevated mRNA expressions of sterol regulatory element-binding transcription factor 1 (SREBP-1c), fatty-acid synthase (FAS), peroxisome proliferator-activated receptor-gamma (PPAR-gamma)1, and PPAR-gamma 2 in HFD-fed mice were significantly attenuated by SC supplementation. Taken together, SC, as a novel natural arginase inhibitor, showed anti -obesity properties by modulating hepatic arginase and NO production and metabolic pathways related to hepatic triglyceride (TG) metabolism.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI-
dc.subjectACTIVATED RECEPTOR-GAMMA-
dc.subjectNITRIC-OXIDE SYNTHASE-
dc.subjectLIVER-DISEASE-
dc.subjectENDOTHELIAL DYSFUNCTION-
dc.subjectVASCULAR DYSFUNCTION-
dc.subjectTRANSCRIPTION FACTOR-
dc.subjectINSULIN-RESISTANCE-
dc.subjectARGINASE-I-
dc.subjectINHIBITION-
dc.subjectEXPRESSION-
dc.titleSemen Cuscutae Administration Improves Hepatic Lipid Metabolism and Adiposity in High Fat Diet-Induced Obese Mice-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Min-Jeong-
dc.identifier.doi10.3390/nu11123035-
dc.identifier.scopusid2-s2.0-85076711849-
dc.identifier.wosid000506917800197-
dc.identifier.bibliographicCitationNUTRIENTS, v.11, no.12-
dc.relation.isPartOfNUTRIENTS-
dc.citation.titleNUTRIENTS-
dc.citation.volume11-
dc.citation.number12-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNutrition & Dietetics-
dc.relation.journalWebOfScienceCategoryNutrition & Dietetics-
dc.subject.keywordPlusACTIVATED RECEPTOR-GAMMA-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusLIVER-DISEASE-
dc.subject.keywordPlusENDOTHELIAL DYSFUNCTION-
dc.subject.keywordPlusVASCULAR DYSFUNCTION-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusINSULIN-RESISTANCE-
dc.subject.keywordPlusARGINASE-I-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordAuthorSemen cuscutae (SC)-
dc.subject.keywordAuthorarginase inhibitor-
dc.subject.keywordAuthornitric oxide (NO)-
dc.subject.keywordAuthorhepatic steatosis-
dc.subject.keywordAuthorobesity-
dc.subject.keywordAuthorperoxisome proliferator-activated receptor (PPAR)-
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