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出 处:《现代生物医学进展》2012年第12期2275-2277,2293,共4页Progress in Modern Biomedicine
摘 要:目的:探讨白藜芦醇对紫外线照射后人皮肤角质形成细胞水通道蛋白3(AQP3)表达的影响及意义。方法:原代培养人皮肤角质形成细胞,采用UVB(20mJ/cm2,40mJ/cm2)照射角质形成细胞后,立即加入0.1mmol/L的白藜芦醇进行干预。RT-PCR检测照射前后角质形成细胞中AQP3 mRNA的表达量,并用羟胺法、比色法、TBA法检测照射前后细胞超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)活性及丙二醛(MDA)含量。结果:1.UVB照射后角质形成细胞AQP3 mRNA的表达量下降(P<0.05),且UVB照射剂量越大,AQP3 mRNA下降越显著(P<0.05)。2.白藜芦醇能显著增加UVB照射后角质形成细胞SOD和GSH-Px活性,并降低细胞MDA含量(P<0.05)。3.白藜芦醇能显著抑制UVB导致的角质形成细胞AQP3 mRNA下降(P<0.05)。结论:白藜芦醇可能通过抑制UVB导致的AQP3 mRNA下降,及提高氧化酶活性、清除自由基的功能,从而延缓皮肤衰老。Objective: To investigate the effect of resveratrol on expression of AQP3 in normal human epidermal keratinocytes (NHEK) irradiated by UVB, and discuss its function in the process of skin aging. Methods: Preparation of skin keratinocyte primary cultures. NHEK irradiated by UVB (20mJ/cm^2, 40mJ/m^2) were immediately treated with 0. 1mmol/L resvetatrol, then observe the change of the expression ofAQP3 mRNA by RT-PCR, and the change of SOD, GSH-Px and MDA by Hydroxyl amine method, colorimetric me- thod and TBA method. Results: 1. The expression level ofAQP3 mRNA after UVB irradiation was significantly lower than its level bef- ore UVB irradiation (P〈0.05). The more the UVB exposure dose it received, the greater the expression level ofAQP3 mRNA decreased. 2. Resvetatrol increased the activity of SOD and GSH-Px, decreased MDA's content of NHEK irradiated by UVB (P〈0.05). 3. Resvetatrol inhibited the decrease ofAQP3 mRNA irradiated by UVB (P〈0.05). Conclusion: Resvetatrol can attenuate UVB-induced down-regulation of AQP3, increase oxydase's activity and clean the free radical, and accordingly to delay skin aging.
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