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Bavachin alleviates diabetic nephropathy in db/db mice by inhibition of oxidative stress and improvement of mitochondria function

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dc.contributor.authorPark, Jisu-
dc.contributor.authorSeo, Eunhui-
dc.contributor.authorJun, Hee-Sook-
dc.date.accessioned2023-05-16T00:41:38Z-
dc.date.available2023-05-16T00:41:38Z-
dc.date.created2023-05-15-
dc.date.issued2023-05-
dc.identifier.issn0753-3322-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/87682-
dc.description.abstractDiabetic nephropathy (DN) is a major complication of diabetes mellitus. Psoralea corylifolia L. seed (PCS) is a traditional medicine effective against various diseases. In this study, we aimed to investigate the effect of bavachin, the major active component of PCS, on DN in db/db mice. Bavachin (10 mg/kg/day) was administered orally to 12-week-old male db/db mice for 6 wk. For in vitro experiments, SV40 MES13 cells were treated with bavachin in the presence of 25 mM glucose. Food and water intake and urine mass were significantly increased in db/db mice compared to wild-type CON mice, but bavachin administration significantly reduced these increases. Urinary microalbumin, blood urea nitrogen, and creatinine clearance which were significantly increased in db/ db mice, were also decreased by bavachin administration. Glomerular area and collagen deposition in the kidney were significantly decreased in db/db mice following bavachin administration. Increased renal levels of fibrotic factors, fibronectin, COL1A1, and alpha-SMA, were reduced following bavachin administration. Protein expressions of antioxidant enzymes, namely SOD2, catalase, and HO-1, and mitochondrial function-related factors, namely SIRT1, PGC1 alpha, Nrf1, and mtTFA, were reduced in the kidney tissues of db/db mice compared to wild-type CON mice, and bavachin administration upregulated these protein expressions. In vitro studies also showed that bavachin decreases mitochondria ROS production, increases the expression of PGC-1 alpha and SIRT1, and decreases the expression of alpha-SMA in high glucose-treated SV40 MES13 cells. Based on these results, bavachin improved DN by inhibiting oxidative stress and enhancing mitochondrial function.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER-
dc.relation.isPartOfBIOMEDICINE & PHARMACOTHERAPY-
dc.titleBavachin alleviates diabetic nephropathy in db/db mice by inhibition of oxidative stress and improvement of mitochondria function-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000956218900001-
dc.identifier.doi10.1016/j.biopha.2023.114479-
dc.identifier.bibliographicCitationBIOMEDICINE & PHARMACOTHERAPY, v.161-
dc.description.isOpenAccessY-
dc.identifier.scopusid2-s2.0-85149822221-
dc.citation.titleBIOMEDICINE & PHARMACOTHERAPY-
dc.citation.volume161-
dc.contributor.affiliatedAuthorPark, Jisu-
dc.contributor.affiliatedAuthorSeo, Eunhui-
dc.contributor.affiliatedAuthorJun, Hee-Sook-
dc.type.docTypeArticle-
dc.subject.keywordAuthorBavachin-
dc.subject.keywordAuthorDiabetic nephropathy-
dc.subject.keywordAuthorOxidative stress-
dc.subject.keywordAuthorMitochondrial function-
dc.subject.keywordAuthorPsoralea corylifolia L-
dc.subject.keywordAuthorseed-
dc.subject.keywordPlusKIDNEY-
dc.subject.keywordPlusBIOGENESIS-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusSIRT1-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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