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Title of Article Optimized models of xenobiotic-induced oxidative stress in HepG2 cells 
Date of Acceptance 24 April 2019 
Journal
     Title of Journal Tropical Journal of Pharmaceutical Research 
     Standard SCOPUS 
     Institute of Journal Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria 
     ISBN/ISSN 1596-5996 
     Volume 18 
     Issue
     Month May
     Year of Publication 2019 
     Page 1001-1007 
     Abstract Purpose: To evaluate the molecular impact of ethanol, sodium selenite, and tert-butyl hydroperoxide (TBHP) on oxidant-antioxidant balance in HepG2 cells to establish an optimized oxidative stress model of HepG2 cells. Methods: HepG2 cells were treated with ethanol (10 - 500 mM) and sodium selenite (1 - 10 µM) for 24 and 48 h and with TBHP (50 - 200 µM) for 3 and 24 h, respectively. Biomarkers for cellular injury, ie, lactate dehydrogenase (LDH), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and malondialdehyde (MDA), and for antioxidant system, i.e., superoxide dismutase (SOD), catalase (CAT), and total glutathione content, were determined. Results: All treatments increased the levels of LDH, AST, ALT, and MDA but decreased SOD and CAT activities and the total glutathione content in HepG2 cells. Oxidative stress was induced by these oxidative stressors in HepG2 cells via oxidant-antioxidant imbalance, with TBHP (100 µM, 3 h) acting as a powerful oxidant based on the minimal time to induce oxidative stress. The antioxidants, ascorbic acid and gallic acid, improved oxidant-antioxidant imbalance against xenobiotic-induced oxidative stress in HepG2 cells. Conclusion: These oxidative stress models are suitable for investigating the antioxidant and/or hepatoprotective potential of chemicals, including natural compounds. 
     Keyword Ethanol, Sodium selenite, Tert-butyl hydroperoxide, Oxidative stressor, Oxidant-antioxidant balance  
Author
607150008-1 Miss YOLLADA SRISET [Main Author]
Pharmaceutical Sciences Doctoral Degree

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