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Effects of Bisphosphonates on Glucose Transport in a Conditionally Immortalized Rat Retinal Capillary Endothelial Cell Line (TR-iBRB Cells)

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dc.contributor.authorLee, Na-Young-
dc.contributor.authorPark, Hyun-Joo-
dc.contributor.authorKang, Young-Sook-
dc.date.available2021-02-22T11:30:11Z-
dc.date.issued2016-01-
dc.identifier.issn1976-9148-
dc.identifier.issn2005-4483-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/9972-
dc.description.abstractThe objective of the present study was to elucidate the effect of bisphosphonates, anti-osteoporosis agents, on glucose uptake in retinal capillary endothelial cells under normal and high glucose conditions. The change of glucose uptake by pre-treatment of bisphosphonates at the inner blood-retinal barrier (iBRB) was determined by measuring cellular uptake of [H-3]3-O-methyl glucose (3-OMG) using a conditionally immortalized rat retinal capillary endothelial cell line (TR-iBRB cells) under normal and high glucose conditions. [H-3]3-OMG uptake was inhibited by simultaneous treatment of unlabeled D-glucose and 3-OMG as well as glucose transport inhibitor, cytochalasin B. On the other hand, simultaneous treatment of alendronate or pamidronate had no significant inhibitory effect on [H-3]3-OMG uptake by TR-iBRB cells. Under high glucose condition of TR-iBRB cells, [H-3]3-OMG uptake was increased at 48 h. However, [H-3]3-OMG uptake was decreased significantly by pre-treatment of alendronate or pannidronate compared with the values for normal and high glucose conditions. Moreover, geranylgeraniol (GGOH), a mevalonate pathway intermediate, increased the uptake of [H-3]3-OMG reduced by bisphosphonates pre-treatment. But, pre-treatment of histamine did not show significant inhibition of [H-3]3-OMG uptake. The glucose uptake may be down regulated by inhibiting the mevalonate pathway with pre-treatment of bisphosphonates in TR-iBRB cells at high glucose condition.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.titleEffects of Bisphosphonates on Glucose Transport in a Conditionally Immortalized Rat Retinal Capillary Endothelial Cell Line (TR-iBRB Cells)-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4062/biomolther.2015.183-
dc.identifier.scopusid2-s2.0-84952685446-
dc.identifier.wosid000367640100013-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.24, no.1, pp 94 - 98-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume24-
dc.citation.number1-
dc.citation.startPage94-
dc.citation.endPage98-
dc.type.docTypeArticle-
dc.identifier.kciidART002060607-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusMEVALONATE PATHWAY-
dc.subject.keywordPlusCHOROIDAL NEOVASCULARIZATION-
dc.subject.keywordPlusTAURINE TRANSPORT-
dc.subject.keywordPlusBOVINE RETINA-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusBARRIER-
dc.subject.keywordPlusPERMEABILITY-
dc.subject.keywordPlusRETINOPATHY-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusHISTAMINE-
dc.subject.keywordAuthorGlucose uptake-
dc.subject.keywordAuthorBisphosphonates-
dc.subject.keywordAuthorInner blood-retinal barrier-
dc.subject.keywordAuthorRetinal capillary endothelial cells-
dc.subject.keywordAuthorMevalonate pathway-
dc.identifier.urlhttp://www.biomolther.org/journal/view.html?volume=24&number=1&spage=94&year=2016-
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