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LIU Rong, YANG Wei-wei, JIANG Yuan-song.et al, . Antioxidant capacity of Pinus sylvestris L.polyphenlols in bovine pulmonary artery endothelial cells[J]. Chinese Journal of Public Health, 2014, 30(1): 80-82. DOI: 10.11847/zgggws2014-30-01-24
Citation: LIU Rong, YANG Wei-wei, JIANG Yuan-song.et al, . Antioxidant capacity of Pinus sylvestris L.polyphenlols in bovine pulmonary artery endothelial cells[J]. Chinese Journal of Public Health, 2014, 30(1): 80-82. DOI: 10.11847/zgggws2014-30-01-24

Antioxidant capacity of Pinus sylvestris L.polyphenlols in bovine pulmonary artery endothelial cells

  • Objective To investigate protective effect of Pinus sylvestris L.polyphenlols extracts on H2O2 induced damage in bovine pulmonary artery endothelial cells (BPAECs).Methods Oxidative damage of BPAECs was induced by H2O2.The BPAECs were divided into control group,H2O2 model group,and high-,midium-,and low-dose polyphenlols groups (0.5,0.1,0.05 mg/mL).The influence of Pinus sylvestris L.polyphenlols extracts on H2O2 induced damage in BPAECs was assessed by measuring the cells' viability with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrozolium bromide(MTT)assay.The superoxide dismutase (SOD);malondialdehyde (MDA),and glutathione peroxidase (GSH-Px)content were determined with assay kits.Results The cell viability of BPAECs decreased (0.71±0.03%)in H2O2 model group compared to that of the control group.The kinases activity of SOD,catalase (CAT),and GSH-Px decreased (24.67±0.69,41.95±0.58,24.38±1.67 U/mg/prot).Meanwhile,the content of MDA increased (5.83±0.04 mmol/mL).In high-dose group (0.5mg/ml),the cell viability of BPAECs raised remarkably (1.64±0.03%)and the kinases activity of SOD,CAT,and GSH-Px improved obviously (53.62±1.24,61.01±1.10,and 48.62±0.82 U/mg/prot).The contents of MDA and protein carbonyl reduced markedly (1.96±0.00 mmol/mL,1.13±0.08 U/mg protein)compared to those of the H2O2 model group.The Results showed a dose-effect relationship.Conclusion The Pinus sylvestris L.polyphenlols extracts possess protective effect on H2O2 induced damage in EPAECs
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