首页> 外文OA文献 >Zerumbone Exhibits Antiphotoaging and Dermatoprotective Properties in Ultraviolet A-Irradiated Human Skin Fibroblast Cells via the Activation of Nrf2/ARE Defensive Pathway
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Zerumbone Exhibits Antiphotoaging and Dermatoprotective Properties in Ultraviolet A-Irradiated Human Skin Fibroblast Cells via the Activation of Nrf2/ARE Defensive Pathway

机译:Zerumbone通过NRF2 /的激活表现出紫外线A-辐射的人体皮肤成纤维细胞中的抗斑和皮肤防护性能/是防御性途径

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摘要

Ultraviolet A (UVA) irradiation (320-400 nm range) triggers deleterious consequences in skin cell microenvironment leading to skin damage, photoaging (premature skin aging), and cancer. The accumulation of intracellular reactive oxygen species (ROS) plays a key role in this effect. With rapid progress in cosmetic health and quality of life, use of safe and highly effective phytochemicals has become a need of the hour. Zerumbone (ZER), a natural sesquiterpene, from Zingiber zerumbet rhizomes is well-known for its beneficial effects. We investigated the antiphotoaging and dermatoprotective efficacies of ZER (2-8 μM) against UVA irradiation (3 J/cm2) and elucidated the underlying molecular mechanisms in human skin fibroblast (HSF) cells. ZER treatment prior to low dose of UVA exposure increased cell viability. UVA-induced ROS generation was remarkably suppressed by ZER with parallel inhibition of MMP-1 activation and collagen III degradation. This was due to the inhibition of AP-1 (c-Fos and c-Jun) translocation. Furthermore, ZER alleviated UVA-induced SA-β-galactosidase activity. Dose- or time-dependent increase of antioxidant genes, HO-1 and γ-GCLC by ZER, was associated with increased expression and nuclear accumulation of Nrf2 as well as decreased cytosolic Keap-1 expressions. Altered luciferase activity of ARE could explain the significance of Nrf2/ARE pathway underlying the dermatoprotective properties of ZER. Pharmacological inhibition of various signaling pathways suppressed nuclear Nrf2 activation in HSF cells confirming that Nrf2 translocation was mediated by ERK, JNK, PI3K/AKT, PKC, AMPK, casein kinase II, and ROS signaling pathways. Moreover, increased basal ROS levels and Nrf2 translocation seem crucial in ZER-mediated Nrf2/ARE signaling pathway. This was also evidenced from Nrf2 knocked-out studies in which ZER was not able to suppress the UVA-induced ROS generation in the absence of Nrf2. This study concluded that in the treatment of UVA-induced premature skin aging, ZER may consider as a desirable food supplement for skin protection and/or preparation of skin care products.
机译:紫外线A(UVA)照射(320-400 nm范围内)触发皮肤细胞微环境从而导致皮肤损伤,光老化(过早皮肤老化)有害的后果,和癌症。细胞内活性氧自由基的积累(ROS)发挥了这种作用了关键作用。随着化妆品的健康和​​生活质量的快速进步,使用安全,高效的植物化学物质已成为需要小时。球姜酮(ZER),天然倍半萜烯,从红球姜根茎是其有益的效果是众所周知的。我们研究了抗UVA照射antiphotoaging和ZER的dermatoprotective功效(2-8μM)(3焦耳/平方厘米),并阐明在人皮肤成纤维(HSF)细胞的潜在分子机制。之前UVA曝光的低剂量治疗寿增加细胞活力。 UVA诱导的ROS产生得到显着通过与ZER MMP-1的活化和胶原III降解的平行抑制抑制。这是由于AP-1的抑制(c-fos和c-Jun的)易位。此外,ZER缓解UVA引起的SA-β半乳糖苷酶活性。剂量或抗氧化基因的时间依赖性增加,HO-1和γ-GCLC由ZER,与增加的表达和Nrf2与核积累以及降低胞质Keap-1的表达相关联。是改变荧光素酶活性可以解释的Nrf2的意义/ ARE通路底层寿的dermatoprotective性能。各种信号传导途径的药理学抑制抑制核的Nrf2活化HSF细胞确认Nrf2的易位通过ERK,JNK,PI3K / AKT,PKC,AMPK,酪蛋白激酶II,和ROS信号传导途径介导的。此外,增加基础ROS水平和Nrf2的易位寿介导的Nrf2显得至关重要/ ARE信号通路。这也证明,从Nrf2的敲除研究中,寿无法抑制Nrf2的情况下的UVA引起的ROS的产生。这项研究的结论是,UVA引起的过早皮肤老化的治疗,寿可考虑作为理想辅食的护肤品保护皮肤和/或制剂。

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