Publication: Pummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence
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Issued Date
2013
Resource Type
File Type
application/pdf
ISSN
1741427X
Other identifier(s)
2-s2.0-84874547456
Rights Holder(s)
มหาวิทยาลัยศรีนครินทรวิโรฒ
Bibliographic Citation
Evidence-based Complementary and Alternative Medicine. Vol 2013, No. (2013), p.-
Suggested Citation
Chularojmontri L., Gerdprasert O., Wattanapitayakul S.K. Pummelo protects doxorubicin-induced cardiac cell death by reducing oxidative stress, modifying glutathione transferase expression, and preventing cellular senescence. Evidence-based Complementary and Alternative Medicine. Vol 2013, No. (2013), p.-. doi:10.1155/2013/254835 Retrieved from: https://hdl.handle.net/20.500.14740/6696
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.
Subject(s)
3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide
Ascorbic acid
Aurantiin
Beta galactosidase
Dichlorodihydrofluorescein diacetate
Doxorubicin
Gallic acid
Glutathione
Glutathione transferase
Hesperidin
Plant extract
Pummelo extract
Reactive oxygen metabolite
Senescence associated beta galactosidase
Unclassified drug
Animal cell
Antioxidant activity
Article
Cell aging
Cell death
Cell protection
Cell survival
Cell viability
Chemical composition
Controlled study
Cytotoxicity
Drug determination
Drug mechanism
Enzyme activity
Enzyme assay
Fruit juice
Heart muscle cell
High performance liquid chromatography
Nonhuman
Oxidative stress
Priority journal
Protein expression
Pummelo
Pummelo fruit juice
Western blotting
Ascorbic acid
Aurantiin
Beta galactosidase
Dichlorodihydrofluorescein diacetate
Doxorubicin
Gallic acid
Glutathione
Glutathione transferase
Hesperidin
Plant extract
Pummelo extract
Reactive oxygen metabolite
Senescence associated beta galactosidase
Unclassified drug
Animal cell
Antioxidant activity
Article
Cell aging
Cell death
Cell protection
Cell survival
Cell viability
Chemical composition
Controlled study
Cytotoxicity
Drug determination
Drug mechanism
Enzyme activity
Enzyme assay
Fruit juice
Heart muscle cell
High performance liquid chromatography
Nonhuman
Oxidative stress
Priority journal
Protein expression
Pummelo
Pummelo fruit juice
Western blotting
