Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/77855
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorCao, Sen_US
dc.creatorDong, XLen_US
dc.creatorHo, MXen_US
dc.creatorYu, WXen_US
dc.creatorWong, KCen_US
dc.creatorYao, XSen_US
dc.creatorWong, MSen_US
dc.date.accessioned2018-08-28T01:35:14Z-
dc.date.available2018-08-28T01:35:14Z-
dc.identifier.issn2072-6643en_US
dc.identifier.urihttp://hdl.handle.net/10397/77855-
dc.language.isoenen_US
dc.publisherMolecular Diversity Preservation International (MDPI)en_US
dc.rights© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Cao, S.; Dong, X.-L.; Ho, M.-X.; Yu, W.-X.; Wong, K.-C.; Yao, X.-S.; Wong, M.-S. Oleanolic Acid Exerts Osteoprotective Effects and Modulates Vitamin D Metabolism. Nutrients 2018, 10, 247 is available at https://dx.doi.org/10.3390/nu10020247en_US
dc.subjectAgingen_US
dc.subjectCalciumen_US
dc.subjectOleanolic aciden_US
dc.subjectOsteoporosisen_US
dc.subjectOvariectomiseden_US
dc.subjectVitamin Den_US
dc.titleOleanolic acid exerts osteoprotective effects and modulates vitamin D metabolismen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage20en_US
dc.identifier.volume10en_US
dc.identifier.issue2en_US
dc.identifier.doi10.3390/nu10020247en_US
dcterms.abstractOleanolic acid (OA) is a triterpenoid with reported bone anti-resorption activities. The present study aimed to characterize its bone protective effects in vivo and to study its effects on vitamin D metabolism, both in vivo and in vitro. OA significantly increased bone mineral density, improved micro-architectural properties, reduced urinary Ca excretion, increased 1,25(OH)2D3 and renal CYP27B1 mRNA expression in mature C57BL/6 ovariectomised (OVX) mice. OA also improved bone properties, Ca balance, and exerted modulatory effects on renal CYP27B1 and CYP24A1 expressions in aged normal female Sprague-Dawley rats. In addition, OA significantly increased renal CYP27B1 mRNA and promoter activity, and suppressed CYP24A1 mRNA and protein expressions in human proximal tubule HKC-8 cells. OA exerted bone protective effects in mature OVX mice and aged female rats. This action on bone might be, at least in part, associated with its effects on Ca and vitamin D metabolism. The present findings suggest that OA is a potential drug candidate for the management of postmenopausal osteoporosis.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationNutrients, Feb. 2018, v. 10, no. 2, 247, p. 1-20en_US
dcterms.isPartOfNutrientsen_US
dcterms.issued2018-02-
dc.identifier.isiWOS:000427540000137-
dc.identifier.scopus2-s2.0-85042502592-
dc.identifier.artn247en_US
dc.identifier.rosgroupid2017004573-
dc.description.ros2017-2018 > Academic research: refereed > Publication in policy or professional journalen_US
dc.description.validate201808 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRA, a1375-
dc.identifier.SubFormID44728-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China (81528024);The Hong Kong Polytechnic University Central Allocation fund (15100015);Collaborative Research Fund PolyU support for shortlisted proposal (1BBAB);Shenzhen Basic Research Program (JCYJ20151030164008764);Research Studentship of the Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
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