Cited 7 times in

Co-administration of ursodeoxycholic acid with rosuvastatin/ezetimibe in a non-alcoholic fatty liver disease model

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dc.contributor.author박준용-
dc.contributor.author배수한-
dc.contributor.author김범경-
dc.contributor.author김승업-
dc.contributor.author김도영-
dc.contributor.author안상훈-
dc.contributor.author이혜원-
dc.contributor.author이다현-
dc.date.accessioned2022-12-22T03:15:37Z-
dc.date.available2022-12-22T03:15:37Z-
dc.date.issued2022-08-
dc.identifier.issn*-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/191826-
dc.description.abstractBackground: Ursodeoxycholic acid (UDCA), statins, and ezetimibe (EZE) have demonstrated beneficial effects against non-alcoholic fatty liver disease (NAFLD). We investigated the efficacy of the combination of UDCA and the mix of rosuvastatin (RSV)/EZE in the treatment of NAFLD. Methods: NAFLD mouse models were developed by injecting thioacetamide, fasting, and high-carbohydrate refeeding, high-fat diet, and choline-deficient L-amino acid-defined high-fat diet (CDAHFD). Low-dose UDCA (L-UDCA; 15 mg/kg) or high-dose UDCA (H-UDCA; 30 mg/kg) was administered with RSV/EZE. We also employed an in vitro model of NAFLD developed using palmitic acid-treated Hepa1c1c7 cells. Results: Co-administration of RSV/EZE with UDCA significantly decreased the collagen accumulation, serum alanine aminotransferase (ALT) levels, and mRNA levels of fibrosis-related markers than those observed in the vehicle group in thioacetamide-treated mice (all P < 0.01). In addition, in the group fasted and refed with a high-carbohydrate diet, UDCA/RSV/EZE treatment decreased the number of apoptotic cells and serum ALT levels compared with those observed in the vehicle group (all P < 0.05). Subsequently, H-UDCA/RSV/EZE treatment decreased the number of ballooned hepatocytes and stearoyl-CoA desaturase 1 (SCD-1) mRNA levels (P = 0.027) in the liver of high-fat diet-fed mice compared with those observed in the vehicle group. In the CDAHFD-fed mouse model, UDCA/RSV/EZE significantly attenuated collagen accumulation and fibrosis-related markers compared to those observed in the vehicle group (all P < 0.05). In addition, UDCA/RSV/EZE treatment significantly restored cell survival and decreased the protein levels of apoptosis-related markers compared to RSV/EZE treatment in palmitic acid-treated Hepa1c1c7 cells (all P < 0.05). Conclusion: Combination therapy involving UDCA and RSV/EZE may be a novel strategy for potent inhibition of NAFLD progression.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherOxford University Press and Science Digestive Pub. Co.-
dc.relation.isPartOfGASTROENTEROLOGY REPORT-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleCo-administration of ursodeoxycholic acid with rosuvastatin/ezetimibe in a non-alcoholic fatty liver disease model-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorSang Hyun Seo-
dc.contributor.googleauthorDa Hyun Lee-
dc.contributor.googleauthorYu Seol Lee-
dc.contributor.googleauthorKyung Joo Cho-
dc.contributor.googleauthorHye Jung Park-
dc.contributor.googleauthorHye Won Lee-
dc.contributor.googleauthorBeom Kyung Kim-
dc.contributor.googleauthorJun Yong Park-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorSang Hoon Ahn-
dc.contributor.googleauthorSoo Han Bae-
dc.contributor.googleauthorSeung Up Kim-
dc.identifier.doi10.1093/gastro/goac037-
dc.contributor.localIdA01675-
dc.contributor.localIdA01798-
dc.contributor.localIdA00487-
dc.contributor.localIdA00654-
dc.contributor.localIdA00385-
dc.contributor.localIdA02226-
dc.contributor.localIdA03318-
dc.relation.journalcodeJ04352-
dc.identifier.eissn2052-0034-
dc.identifier.pmid35982712-
dc.subject.keywordezetimibe-
dc.subject.keywordnon-alcoholic fatty liver disease-
dc.subject.keywordnon-alcoholic steatohepatitis-
dc.subject.keywordrosuvastatin-
dc.subject.keywordursodeoxycholic acid-
dc.contributor.alternativeNamePark, Jun Yong-
dc.contributor.affiliatedAuthor박준용-
dc.contributor.affiliatedAuthor배수한-
dc.contributor.affiliatedAuthor김범경-
dc.contributor.affiliatedAuthor김승업-
dc.contributor.affiliatedAuthor김도영-
dc.contributor.affiliatedAuthor안상훈-
dc.contributor.affiliatedAuthor이혜원-
dc.citation.volume10-
dc.citation.startPagegoac037-
dc.identifier.bibliographicCitationGASTROENTEROLOGY REPORT, Vol.10 : goac037, 2022-08-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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