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dc.contributor.authorChularojmontri L.
dc.contributor.authorGerdprasert O.
dc.contributor.authorWattanapitayakul S.K.
dc.date.accessioned2021-04-05T03:33:09Z-
dc.date.available2021-04-05T03:33:09Z-
dc.date.issued2013
dc.identifier.issn1741427X
dc.identifier.other2-s2.0-84874547456
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14092-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84874547456&doi=10.1155%2f2013%2f254835&partnerID=40&md5=ebb6a1a886e477ad23e51720f25f4cdf
dc.description.abstractCitrus flavonoids have been shown to reduce cardiovascular disease (CVD) risks prominently due to their antioxidant effects. Here we investigated the protective effect of pummelo (Citrus maxima, CM) fruit juice in rat cardiac H9c2 cells against doxorubicin (DOX-) induced cytotoxicity. Four antioxidant compositions (ascorbic acid, hesperidin, naringin, and gallic acid) were determined by HPLC. CM significantly increased cardiac cell survival from DOX toxicity as evaluated by MTT assay. Reduction of cellular oxidative stress was monitored by the formation of DCF fluorescent product and total glutathione (GSH) levels. The changes in glutathione-S-transferase (GST) activity and expression were determined by enzyme activity assay and Western blot analysis, respectively. Influence of CM on senescence-associated β-galactosidase activity (SA-β-gal) was also determined. The mechanisms of cytoprotection involved reduction of intracellular oxidative stress, maintaining GSH availability, and enhanced GST enzyme activity and expression. DOX-induced cellular senescence was also attenuated by long-term CM treatment. Thus, CM fruit juice can be promoted as functional fruit to protect cells from oxidative cell death, enhance the phase II GSTP enzyme activity, and decrease senescence phenotype population induced by cardiotoxic agent such as DOX. © 2013 L. Chularojmontri et al.
dc.subject3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide
dc.subjectascorbic acid
dc.subjectaurantiin
dc.subjectbeta galactosidase
dc.subjectdichlorodihydrofluorescein diacetate
dc.subjectdoxorubicin
dc.subjectgallic acid
dc.subjectglutathione
dc.subjectglutathione transferase
dc.subjecthesperidin
dc.subjectplant extract
dc.subjectpummelo extract
dc.subjectreactive oxygen metabolite
dc.subjectsenescence associated beta galactosidase
dc.subjectunclassified drug
dc.subjectanimal cell
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectcell aging
dc.subjectcell death
dc.subjectcell protection
dc.subjectcell survival
dc.subjectcell viability
dc.subjectchemical composition
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdrug determination
dc.subjectdrug mechanism
dc.subjectenzyme activity
dc.subjectenzyme assay
dc.subjectfruit juice
dc.subjectheart muscle cell
dc.subjecthigh performance liquid chromatography
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectpummelo
dc.subjectpummelo fruit juice
dc.subjectWestern blotting
dc.titlePummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationEvidence-based Complementary and Alternative Medicine. Vol 2013, No. (2013), p.-
dc.identifier.doi10.1155/2013/254835
Appears in Collections:Scopus 1983-2021

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