中药金百美颜方对中波紫外诱导HaCaT细胞氧化损伤和光老化的保护作用

Protective Effects of Jin Bai Mei Yan Prescription on Oxidative Damage and Photoaging Induced by Ultraviolet B in HaCaT Cells

  • 摘要:
    目的中波紫外线(UVB)主要作用于皮肤表皮,引起角质形成细胞氧化损伤和凋亡,中药金百美颜方中含有多种抗氧化成分,因此本文主要观察金百美颜方对中波紫外诱导HaCaT细胞氧化损伤的保护作用。
    方法将HaCaT细胞分为空白组、模型(UVB)组、阳性(维生素E)组、金百美颜方低剂量组 (160 μg/mL)、金百美颜方中剂量组 (800 μg/mL)、金百美颜方高剂量组 (1 600 μg/mL),先用UVB照射细胞,再用金百美颜方处理HaCaT细胞24 h;MTT法检测细胞生存率,实时无标记细胞功能分析仪检测细胞增殖率,同时采用ELISA法测定细胞内活性氧(ROS)、脂质过氧化物丙二醛(MDA)水平、谷胱甘肽(GSH)和羟脯氨酸(HYP)水平,以及抗氧化酶超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。
    结果与模型组相比,金百美颜方各剂量组干预后HaCaT细胞生存率明显提高 (P < 0.05),金百美颜方可促进HaCaT细胞的增殖,降低HaCaT细胞中MDA、ROS含量,升高HaCaT细胞中SOD、CAT、GSH、HYP的含量。
    结论中药金百美颜方对UVB诱导HaCaT细胞氧化损伤具有较好的保护作用。

     

    Abstract:
    ObjectiveUltraviolet B (UVB) mainly acts on the skin epidermis, causing oxidative damage and apoptosis of keratinocytes. Jin Bai Mei Yan Prescription (JBMYP) comprises a variety of antioxidant traditional Chinese medicines (TCM). In this study, we aimed to evaluate the effects of JBMYP on the oxidative damage induced by UVB in human immortalized epidermal keratinocytes (HaCaT) cells.
    MethodsHaCaT cells were divided into six groups: control group, model (UVB) group, positive (UVB + vitamin E) group, UVB + JBMYP low dose group (160 μg/mL), UVB + JBMYP mode-rate dose group (800 μg/mL), and UVB + JBMYP high dose group (1 600 μg/mL). HaCaT cells were irradiated with UVB and treated with JBMYP for 24 h. Methyl thiazolyl tetrazolium (MTT) assay and real-time unlabeled cell function analyzer were used to assess the cell survival and proliferation rates, respectively. At the same time, the levels of intracellular reactive oxygen species (ROS), lipid peroxide malondialdehyde (MDA), glutathione (GSH), and hydroxyproline (HYP), as well as the activities of antioxidant enzyme superoxide dismutase (SOD) and catalase (CAT) were evaluated using enzyme linked immunosorbent assay (ELISA).
    ResultsCompared with the model group, the survival rate of HaCaT cells in each dosage group of JBMYP was significantly improved (P < 0.05). Further, JBMYP could promote the proliferation of HaCaT cells, leading to a reduction in the contents of MDA and ROS, and increase in the contents of SOD, CAT, GSH and HYP in HaCaT cells.
    ConclusionsJBMYP has enhanced protective effect on oxidative damage induced by UVB in HaCaT cells.

     

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