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Topical Bixin Confers NRF2-Dependent Protection Against Photodamage and Hair Graying in Mouse Skin

机译:局部Bixin赋予NRF2依赖性保护,防止小鼠皮肤发生光损伤和头发变白

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摘要

Environmental exposure to solar ultraviolet (UV) radiation causes acute photodamage, premature aging, and skin cancer, attributable to UV-induced genotoxic, oxidative, and inflammatory stress. The transcription factor NRF2 [nuclear factor erythroid 2 (E2)-related factor 2] is the master regulator of the cellular antioxidant response protecting skin against various environmental stressors including UV radiation and electrophilic pollutants. NRF2 in epidermal keratinocytes can be activated using natural chemopreventive compounds such as the apocarotenoid bixin, an FDA-approved food additive and cosmetic ingredient from the seeds of the achiote tree (Bixa orellana). Here, we tested the feasibility of topical use of bixin for NRF2-dependent skin photoprotection in two genetically modified mouse models [SKH1 and C57BL/6J (Nrf2+/+ versus Nrf2-/-)]. First, we observed that a bixin formulation optimized for topical NRF2 activation suppresses acute UV-induced photodamage in Nrf2+/+ but not Nrf2-/- SKH1 mice, a photoprotective effect indicated by reduced epidermal hyperproliferation and oxidative DNA damage. Secondly, it was demonstrated that topical bixin suppresses PUVA (psoralen + UVA)-induced hair graying in Nrf2+/+ but not Nrf2-/- C57BL/6J mice. Collectively, this research provides the first in vivo evidence that topical application of bixin can protect against UV-induced photodamage and PUVA-induced loss of hair pigmentation through NRF2 activation. Topical NRF2 activation using bixin may represent a novel strategy for human skin photoprotection, potentially complementing conventional sunscreen-based approaches.
机译:环境暴露于太阳紫外线(UV)会导致急性光损伤,过早衰老和皮肤癌,这归因于紫外线引起的遗传毒性,氧化和炎性应激。转录因子NRF2 [与核因子红系2(E2)相关的因子2]是细胞抗氧化剂反应的主要调节剂,可保护皮肤免受各种环境胁迫,包括紫外线辐射和亲电子污染物。表皮角质形成细胞中的NRF2可以使用天然的化学预防化合物(如类胡萝卜素联苯胺)来激活,该化合物是FDA批准的食品添加剂,是来自壳树(Bixa orellana)种子的化妆品成分。在这里,我们测试了在两种转基因小鼠模型[SKH1和C57BL / 6J(Nrf2 + / + 与Nrf2 -/-< / sup>)]。首先,我们观察到一种针对局部NRF2活化而优化的bixin制剂可抑制Nrf2 + / + 中的急性UV诱导的光损伤,但不能抑制Nrf2 -/- SKH1小鼠,这具有光保护作用通过减少表皮过度增殖和氧化性DNA损伤来指示。其次,证明了局部联蛋白抑制了Nrf2 + / + 中的PUVA(补骨脂素+ UVA)诱导的头发变白,但不抑制Nrf2 -/- C57BL / 6J小鼠。总的来说,这项研究提供了第一个体内证据,即局部应用联蛋白可以通过NRF2激活来防止紫外线引起的光损伤和PUVA引起的头发色素沉着的损失。使用联蛋白的局部NRF2激活可能代表了人类皮肤光保护的新策略,可能会补充传统的基于防晒霜的方法。

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