Institute of Nutrition, College of Biopharmaceutical and Food Sciences, China Medical University, Taichung 40402, Taiwan.
Graduate Institute of Veterinary Pathology, National Chung-Hsing University, Taichung 402, Taiwan.
Biochem Pharmacol. 2018 Feb;148:130-146. doi: 10.1016/j.bcp.2017.12.014. Epub 2017 Dec 20.
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 μM) substantially suppressed UVA (15 J/cm)-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 γ-glutamyl cysteine ligase (γ-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 μg/day) significantly ameliorated UVA (15 J/cm/every 2-day/14-day) cytotoxicity via increased nuclear localization of Nrf2 and Nrf2-dependent antioxidant genes (HO-1 and γ-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.
紫外线 A(UVA)辐射会深入真皮并通过产生过多的活性氧物种(ROS)而损害细胞成分,从而加速光老化和皮肤癌,对皮肤有毒害作用。我们评估了姜烯酮(姜黄属植物的天然倍半萜)在 UVA 照射的人皮肤角质形成细胞(HaCaT)和小鼠表皮中的皮肤保护功效。姜烯酮预处理(2-10 μM)可显著抑制 UVA(15 J/cm)诱导的 HaCaT 细胞死亡和乳酸脱氢酶释放,呈剂量依赖性。UVA 诱导的过量 ROS 产生、DNA 单链断裂、凋亡性 DNA 片段化和 Bax/Bcl-2 比值失调在角质形成细胞中也被姜烯酮显著逆转。姜烯酮介导的细胞保护特性与核因子-E2 相关因子-2(Nrf2)的核易位增加和抗氧化反应元件(ARE)荧光素酶活性升高有关。在姜烯酮处理的角质形成细胞中,Nrf2/ARE 信号的激活伴随着血红素加氧酶-1(HO-1)和γ-谷氨酰半胱氨酸连接酶(γ-GCLC)基因的诱导。姜烯酮诱导的 Nrf2 转录激活是通过 p38 MAPK、PI3K/AKT 和 PKC 信号级联介导的。值得注意的是,Nrf2 沉默(siRNA 转染)显著减弱了姜烯酮介导的细胞保护作用,这表现在 UVA 照射后抗氧化基因失控、ROS/凋亡性 DNA 片段化和角质形成细胞死亡。体内证据表明,姜烯酮处理裸鼠(55 和 110 μg/天)通过增加 Nrf2 的核定位和 Nrf2 依赖性抗氧化基因(HO-1 和 γ-GCLC),显著改善了 UVA(15 J/cm/每 2 天/14 天)的细胞毒性。我们的研究结果强调了 Nrf2/ARE 信号在姜烯酮诱导抗氧化基因对抗 UVA 毒性中的重要性。分子证据表明,姜烯酮可以作为一种天然药物来治疗/预防 UVA 诱导的皮肤损伤/光老化。