Publication:
Pummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence

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.date.issuedBE2556
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.format.mimetypeapplication/pdf
dc.identifier.citationEvidence-based Complementary and Alternative Medicine. Vol 2013, No. (2013), p.-
dc.identifier.doi10.1155/2013/254835
dc.identifier.issn1741427X
dc.identifier.other2-s2.0-84874547456
dc.identifier.urihttps://hdl.handle.net/20.500.14740/6696
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.other3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide
dc.subject.otherAscorbic acid
dc.subject.otherAurantiin
dc.subject.otherBeta galactosidase
dc.subject.otherDichlorodihydrofluorescein diacetate
dc.subject.otherDoxorubicin
dc.subject.otherGallic acid
dc.subject.otherGlutathione
dc.subject.otherGlutathione transferase
dc.subject.otherHesperidin
dc.subject.otherPlant extract
dc.subject.otherPummelo extract
dc.subject.otherReactive oxygen metabolite
dc.subject.otherSenescence associated beta galactosidase
dc.subject.otherUnclassified drug
dc.subject.otherAnimal cell
dc.subject.otherAntioxidant activity
dc.subject.otherArticle
dc.subject.otherCell aging
dc.subject.otherCell death
dc.subject.otherCell protection
dc.subject.otherCell survival
dc.subject.otherCell viability
dc.subject.otherChemical composition
dc.subject.otherControlled study
dc.subject.otherCytotoxicity
dc.subject.otherDrug determination
dc.subject.otherDrug mechanism
dc.subject.otherEnzyme activity
dc.subject.otherEnzyme assay
dc.subject.otherFruit juice
dc.subject.otherHeart muscle cell
dc.subject.otherHigh performance liquid chromatography
dc.subject.otherNonhuman
dc.subject.otherOxidative stress
dc.subject.otherPriority journal
dc.subject.otherProtein expression
dc.subject.otherPummelo
dc.subject.otherPummelo fruit juice
dc.subject.otherWestern blotting
dc.titlePummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84874547456&doi=10.1155%2f2013%2f254835&partnerID=40&md5=ebb6a1a886e477ad23e51720f25f4cdf

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