Quercetin in combating H_2O_2 induced early cell apoptosis and mitochondrial damage to normal human keratinocytes
摘要Background Oxidative stress plays an important role in the pathogenesis of epidermal diseases. This study aimed to investigate the effects of quercetin on the anti-oxidative response and on mitochondrial protection in cultured normal human keratinocytes. Methods Cultured HaCaT cells were treated with different concentrations of H_2O_2 (0, 50, 100, 250, 500 μmol/L) for different periods of time (0.5, 1,2,4 hours) to establish an oxidative stress model. The cultured HaCaT cells were randomly assigned to control, H_2O_2, and quercetin+H_2O_2 groups. For the quercetin groups, the cells were treated with different concentrations of quercetin (0,10, 25, 50 μmol/L) before exposure to H_2O_2. Morphological changes of the cells were observed under an inverted microscope and an electron microscope. The cell viability was detected by the MTT method. The cell apoptosis (AnnexinV/propidium iodide double stain) and mitochondrial membrane potential (△ψm) changes were detected by flow cytometry. Results An oxidative stress model of HaCaT cells was established under a suitable concentration (250 μmol/L) and treated time of H_2O_2 (2 hours). The cell viability and △ψm decreased in a concentration-dependent and time-dependent manner while the percentage of apoptotic cells significantly increased in the H_2O_2 groups compared with the control group (P<0.05). The cell viability and △ψm of the quercetin treated group increased (P<0.05) and the percentage of apoptotic cells decreased at concentrations of 1-50 μmol/L quercetin (P<0.01) compared with H_2O_2 treated group. Conclusion Quercetin can relieve the cell damage and apoptosis from H_2O_2 induced injury to HaCaT cells by anti-oxidation and mitochondrial protection.
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