4.6 Article

Quercetin and Resveratrol Decrease the Inflammatory and Oxidative Responses in Human Ocular Surface Epithelial Cells

期刊

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
卷 56, 期 4, 页码 2709-2719

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ASSOC RESEARCH VISION OPHTHALMOLOGY INC
DOI: 10.1167/iovs.15-16595

关键词

quercetin; resveratrol; inflammation; dry eye; antioxidant

资金

  1. ayudas FPI-UVa, University of Valladolid, Spain

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PURPOSE. To determine the anti-inflammatory and antioxidant effects of quercetin (QCT) and/or resveratrol (RES) on human conjunctival (IOBA-NHC) and corneal (HCE) epithelial cell lines. METHODS. IOBA-NHC and HCE cells were treated with QCT (0.5-25 mu M), RES (0.5-50 mu M) and a low-dose mixture of QCT (0.5 mu M) and RES (5 mu M) (QCT+RES) and stimulated with either TNF-alpha or ultraviolet (UV)-B radiation. Cytokine production (IL-6, IL-8, IP-10, and VEGF) was analyzed by an immune bead-based array, and intracellular reactive oxygen species (ROS) production was determined by a H2DCF-DA dye assay. RESULTS. Stimulation of IOBA-NHC and HCE cells with TNF-alpha induced an increase of IL-6, IL-8, and IP-10 secretion in both cell lines. Quercetin and RES decreased IL-6 and IP-10 secretion in a dose-dependent manner in both cell lines. Interleukin-8 secretion was also inhibited in a dose-dependent manner by QCT in HCE, but only at 20 and 25 mu M QCT and 50 mu M RES in IOBA-NHC and at 50 mu M RES in HCE. QCT+RES decreased IL-6 and IL-8 secretion (P < 0.01 and P < 0.05, respectively) in IOBA-NHC cells. Ultraviolet-B induced a significant increase of ROS in both cell lines (P < 0.01 and P < 0.001 for IOBA-NHC and HCE cells, respectively), which was significantly decreased in a dose-dependent manner by QCT and RES in HCE cells. Reactive oxygen species production in IOBA-NHC cells was inhibited (P < 0.05) by 50 mu M RES. CONCLUSIONS. Quercetin and RES have anti-inflammatory and antioxidant effects on IOBA-NHC and HCE cells. These in vitro data suggest that both polyphenols may have a therapeutic potential in the treatment of inflammatory ocular surface diseases.

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