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首页> 外文期刊>Antioxidants >The Skin-Whitening Effects of Ectoine via the Suppression of α-MSH-Stimulated Melanogenesis and the Activation of Antioxidant Nrf2 Pathways in UVA-Irradiated Keratinocytes
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The Skin-Whitening Effects of Ectoine via the Suppression of α-MSH-Stimulated Melanogenesis and the Activation of Antioxidant Nrf2 Pathways in UVA-Irradiated Keratinocytes

机译:通过抑制α-MSH刺激的黑素生成的皮肤 - 美化效应和UVA辐照角质形成细胞抗氧化NRF2途径的激活

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Ultraviolet A (UVA)-irradiation induced reactive oxygen species (ROS) production mediates excessive melanogenesis in skin cells leading to pigmentation. We demonstrated the depigmenting and anti-melanogenic effects of Ectoine, a natural bacterial osmolyte, in UVA-irradiated human (HaCaT) keratinocytes, and the underlying molecular mechanisms were elucidated. HaCaT cells were pre-treated with low concentrations of Ectoine (0.5–1.5 μM) and assayed for various depigmenting and anti-melanogenic parameters. This pre-treatment significantly downregulated ROS generation, α-melanocyte-stimulating hormone (α-MSH) production, and proopiomelanocortin (POMC) expression in UVA-irradiated HaCaT cells. Also, antioxidant heme oxygenase-1 (HO-1), NAD(P)H dehydrogenase [quinone 1] (NQO-1), and γ-glutamate-cysteine ligase catalytic subunit (γ-GCLC) protein expressions were mediated via the nuclear translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) whose knockdown indeed impaired this effect signifying the importance of the Nrf2 pathway. Ectoine was mediating the activation of Nrf2 via the p38, protein kinase B (also known as AKT), protein kinase C (PKC), and casein kinase II protein kinase (CKII) pathways. The conditioned medium obtained from the Ectoine pre-treated and UVA-irradiated HaCaT cells downregulated the tyrosinase, tyrosinase-related protein-1 and -2 (TRP-1/-2), cyclic AMP (c-AMP) protein kinase, c-AMP response element-binding protein (CREB), and microphthalmia-associated transcription factor (MITF) expressions leading to melanoma B16F10 cells having inhibited melanin synthesis. Interestingly, this anti-melanogenic effect in α-MSH-stimulated B16F10 cells was observable only at 50–400 μM concentrations of Ectoine, signifying the key role played by Ectoine (0.5–1 μM)-treated keratinocytes in skin whitening effects. We concluded that Ectoine could be used as an effective topical natural cosmetic agent with depigmenting and anti-melanogenic efficacy.
机译:紫外线A(UVA) - 辐射诱导的活性氧物质(ROS)生产在导致色素沉着的皮肤细胞中介导过量的黑素生成。我们证明了UVA辐照的人(HACAT)角质形成细胞中胞外,天然细菌Osmolyte的脱落和抗批发效应,并阐明了下面的分子机制。用低浓度的胞外(0.5-1.5μm)预处理HaCAT细胞,并测定各种脱沉和抗溶素参数。这种预处理明显下调的ROS生成,α-黑素细胞刺激激素(α-MSH)生产和ProOpioMelanocortin(POMC)表达在UVA辐照的HaCAT细胞中。此外,通过核介导抗氧化血红素氧酶-1(HO-1),NAD(P)H脱氢酶[醌1](NQO-1)和γ-谷氨酸 - 半胱氨酸连接酶催化亚基(γ-GCLC)蛋白表达核因子红细胞2相关因子2(NRF2)的易位,其敲低确实损害了这一效果意味着NRF2途径的重要性。 Ectoine通过P38,蛋白激酶B(也称为AKT),蛋白激酶C(PKC)和酪蛋白激酶II蛋白激酶(CKII)途径介导NRF2的活化。从胞外预处理和UVA辐照的HaCAT细胞获得的调节培养基下调了酪氨酸酶,酪氨酸酶相关蛋白-1和-2(TRP-1 / -2),环形放大术(C-AMP)蛋白激酶,C- AMP响应元素结合蛋白(CREB)和细胞膜相关的转录因子(MITF)表达,其导致黑色素瘤B16F10细胞具有抑制黑色素合成。有趣的是,这种α-MSH刺激的B16F10细胞中的这种抗批发效果仅在50-400μm浓度的胞外观察到,意味着胞外(0.5-1μm) - 治疗皮肤美白效应中的角质形成细胞的关键作用。我们得出结论,胞外可以用作具有脱粒和抗批量疗效的有效局部天然化妆品。

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