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

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dc.contributor.author Chularojmontri L.
dc.contributor.author Gerdprasert O.
dc.contributor.author Wattanapitayakul S.K.
dc.date.accessioned 2021-04-05T03:33:09Z
dc.date.available 2021-04-05T03:33:09Z
dc.date.issued 2013
dc.identifier.issn 1741427X
dc.identifier.other 2-s2.0-84874547456
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/14092
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-84874547456&doi=10.1155%2f2013%2f254835&partnerID=40&md5=ebb6a1a886e477ad23e51720f25f4cdf
dc.description.abstract Citrus 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.subject 3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide
dc.subject ascorbic acid
dc.subject aurantiin
dc.subject beta galactosidase
dc.subject dichlorodihydrofluorescein diacetate
dc.subject doxorubicin
dc.subject gallic acid
dc.subject glutathione
dc.subject glutathione transferase
dc.subject hesperidin
dc.subject plant extract
dc.subject pummelo extract
dc.subject reactive oxygen metabolite
dc.subject senescence associated beta galactosidase
dc.subject unclassified drug
dc.subject animal cell
dc.subject antioxidant activity
dc.subject article
dc.subject cell aging
dc.subject cell death
dc.subject cell protection
dc.subject cell survival
dc.subject cell viability
dc.subject chemical composition
dc.subject controlled study
dc.subject cytotoxicity
dc.subject drug determination
dc.subject drug mechanism
dc.subject enzyme activity
dc.subject enzyme assay
dc.subject fruit juice
dc.subject heart muscle cell
dc.subject high performance liquid chromatography
dc.subject nonhuman
dc.subject oxidative stress
dc.subject priority journal
dc.subject protein expression
dc.subject pummelo
dc.subject pummelo fruit juice
dc.subject Western blotting
dc.title Pummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Evidence-based Complementary and Alternative Medicine. Vol 2013, No. (2013), p.-
dc.identifier.doi 10.1155/2013/254835


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