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Zerumbone protects human skin keratinocytes against UVA-irradiated damages through Nrf2 induction

机译:Zerumbone通过NRF2诱导保护人体皮肤角膜细胞免受UVA辐照的损害

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Ultraviolet A (UVA) irradiation is toxic to skin as it penetrates deep into the dermis and damages cellular components through excessive reactive oxygen species (ROS) production, which accelerates photoaging and skin cancer. We evaluated the dermato-protective efficacies of zerumbone (natural sesquiterpene of Zingiber zerumbet) in UVA-irradiated human skin keratinocyte (HaCaT) cells and mouse epidermis. Zerumbone pretreatment (2-10 mu M) substantially suppressed UVA (15 K/cm(2))-induced HaCaT cell death and lactate dehydrogenase release in a dose-dependent manner. UVA-induced excessive ROS production, DNA single-strand breaks, apoptotic DNA fragmentation and a dysregulated Bax/Bcl-2 ratio were remarkably reversed by zerumbone in keratinocytes. Zerumbone-mediated cytoprotective properties were associated with increased nuclear translocation of nuclear factor-E2-related factor-2 (Nrf2) and elevated antioxidant response element (ARE) luciferase activity. Activation of Nrf2/ARE signaling was accompanied by induction of heme oxygenase-1 (HO-1) and gamma-glutamyl cysteine ligase (gamma-GCLC) genes in zerumbone-treated keratinocytes. Zerumbone-induced Nrf2 transcriptional activation was mediated by the p38 MAPK, PI3K/AKT and PKC signaling cascades. Notably, silencing of Nrf2 (siRNA transfection) significantly diminished zerumbone-mediated cytoprotective effects, as evidenced by impaired antioxidant genes, uncontrolled ROS/apoptotic DNA fragmentation and keratinocytes death, following UVA irradiation. In vivo evidence demonstrated that zerumbone treatment to nude mice (55 and 110 g/day) significantly ameliorated UVA (15 J/cm(2)/every 2-day/14-day) cytotoxicity via increased nuclear localization of Nrf2 and Nrf2-dependent antioxidant genes (HO-1 and gamma-GCLC) in UVA-treated skin tissues. Our findings emphasized the significance of Nrf2/ARE-signaling in zerumbone-mediated induction of antioxidant genes against UVA-toxicity. The molecular evidence suggests zerumbone can be a natural medicine to treat/prevent UVA-induced skin damage/photoaging. (C) 2017 Elsevier Inc. All rights reserved.
机译:紫外线A(UVA)辐射对皮肤有毒,因为它深入真皮,通过过量的反应性氧物种(ROS)生产来损坏细胞组分,从而加速了光手册和皮肤癌。我们在UVA辐照的人体皮肤角膜细胞(HACAT)细胞和小鼠表皮中,评估了Zerumbone(Zingiber Zerumbet的天然SesquiterPene)的皮肤保护效果。 Zerumbone预处理(2-10μm)基本上抑制的UVA(15k / cm(2)) - 诱导的Hacat细胞死亡和乳酸脱氢酶以剂量依赖性方式释放。 UVA诱导的过量的ROS生产,DNA单链断裂,凋亡DNA碎片和具有疑难解的BAX / BCL-2的比例显着逆转了角蛋白细胞。 Zerumbone介导的细胞保护性与核因子-E2相关因子-2(NRF2)的核转位增加有关,升高的抗氧化反应元素(是)荧光素酶活性。 NRF2 /是信号传导的活化伴有血红素氧酶-1(HO-1)和γ-谷氨酰胺半胱氨酸连接酶(Gamma-gclc)基因在Zerumbone处理的角质形成细胞中的诱导。 Zerumbone诱导的NRF2转录激活由P38 MAPK,PI3K / AKT和PKC信号级联介导。值得注意的是,NRF2(siRNA转染)的沉默显着降低了Zerumbone介导的细胞保护作用,如受损的抗氧化基因,不受控制的ROS /凋亡DNA碎裂和角质细胞死亡所证明的,在UVA辐照后,抗氧化基因和角蛋白细胞死亡。在体内证据证明,通过增加NRF2和NRF2依赖性的核定位抗氧化基因(HO-1和γ-GCLC)在UVA处理的皮肤组织中。我们的研究结果强调了NRF2 /患者在Zerumbone介导的抗氧化基因诱导抗氧化基因免受UVA毒性的重要性。分子证据表明Zerumbone可以是治疗/预防uva诱导的皮肤损伤/光电手册的天然药物。 (c)2017年Elsevier Inc.保留所有权利。

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