Chaiprasongsuk Anyamanee, Onkoksoong Tasanee, Pluemsamran Thanyawan, Limsaengurai Saowalak, Panich Uraiwan
Department of Pharmacology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Department of Pharmacology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Redox Biol. 2016 Aug;8:79-90. doi: 10.1016/j.redox.2015.12.006. Epub 2015 Dec 19.
Dietary phenolics may play a protective role in UV-mediated skin pigmentation through their antioxidant and UV-absorbing actions. In this study, we investigated whether genetic silencing of Nrf2, regulating the transcription of antioxidant genes, affected melanogenesis in primary human epidermal melanocytes (HEMn) and B16F10 melanoma cells subjected to UVA (8J/cm(2)) exposure. Then, we explored the antimelanogenic actions of phenolics; caffeic acid (CA) and ferulic acid (FA) providing partial UVA protection; quercetin (QU) and rutin (RU) providing strong UVA protection and; avobenzone (AV), an efficient UVA filter, in association with modulation of Nrf2-mediated antioxidant defenses in response to UVA insults in B16F10 cells. Upon oxidative insults, Nrf2 silencing promoted melanogenesis in both HEMn and B16F10 cells irradiated with UVA. Stimulation of melanogenesis by UVA correlated with increased ROS and oxidative DNA damage (8-OHdG), GSH depletion as well as a transient downregulation of Nrf2 nuclear translocation and of Nrf2-ARE signaling in B16F10 cells. All test compounds exerted antimelanogenic effects with respect to their abilities to reverse UVA-mediated oxidative damage as well as downregulation of Nrf2 activity and its target antioxidants (GCLC, GST and NQO1) in B16F10 cells. In conclusion, defective Nrf2 may promote melanogenesis under UVA irradiation through oxidative stress mechanisms. Compounds with antioxidant and/or UVA absorption properties could protect against UVA-induced melanogenesis through indirect regulatory effect on Nrf2-ARE pathway.
膳食酚类物质可能通过其抗氧化和紫外线吸收作用,在紫外线介导的皮肤色素沉着中发挥保护作用。在本研究中,我们调查了调节抗氧化基因转录的Nrf2基因沉默是否会影响原代人表皮黑素细胞(HEMn)和接受UVA(8J/cm²)照射的B16F10黑色素瘤细胞中的黑素生成。然后,我们探究了酚类物质的抗黑素生成作用;咖啡酸(CA)和阿魏酸(FA)提供部分UVA防护;槲皮素(QU)和芦丁(RU)提供较强的UVA防护;以及阿伏苯宗(AV),一种高效的UVA滤光剂,与B16F10细胞中Nrf2介导的抗氧化防御对UVA损伤的调节作用相关。在氧化损伤时,Nrf2沉默促进了UVA照射的HEMn和B16F10细胞中的黑素生成。UVA对黑素生成的刺激与B16F10细胞中活性氧增加、氧化性DNA损伤(8-OHdG)、谷胱甘肽耗竭以及Nrf2核转位和Nrf2-ARE信号的短暂下调相关。所有测试化合物均发挥了抗黑素生成作用,这与其逆转UVA介导的氧化损伤以及下调B16F10细胞中Nrf2活性及其靶标抗氧化剂(GCLC、GST和NQO1)的能力有关。总之,有缺陷的Nrf2可能通过氧化应激机制在UVA照射下促进黑素生成。具有抗氧化和/或UVA吸收特性的化合物可通过对Nrf2-ARE途径的间接调节作用,预防UVA诱导的黑素生成。