Photomedicine and Photobiology Unit, Department of Dermatology, Henry Ford Hospital, Detroit, MI.
Graduate Medical Education, Broward Health Medical Center, Fort Lauderdale, FL.
Photochem Photobiol. 2022 Mar;98(2):455-460. doi: 10.1111/php.13525. Epub 2021 Oct 4.
The role of topical antioxidants (AOs) on visible light plus ultraviolet A1 (VL+UVA1)-induced skin changes were evaluated. Twenty subjects with skin phototypes (SPTs) I-VI had placebo and concentrations of an AO blend applied to their back (AO 0.5%, 1.0% and 2.0%). Treated and control sites were irradiated with VL+UVA1. Colorimetric and diffuse reflectance spectroscopy (DRS) assessments were performed immediately, 24 h and 7 days after irradiation. Subjects with SPT I-III had erythema that faded within 24 h, while SPT IV-VI had persistent pigmentation. SPT I-III demonstrated significantly less erythema at the 2% AO site while SPT IV-VI demonstrated significantly less immediate pigmentation at 2% AO site and less pigmentation (approaching significance, P = 0.07) on day 7 compared with control. Immunohistochemistry from biopsies of 2% AO and placebo at 24 h did not demonstrate a significant change in COX-2 or MART-1 for any SPT. There was a decrease in cyclin D1 for SPT IV-VI which was approaching significance (P = 0.06) but not for SPT I-III. The results indicate that topical AO inhibits erythema in SPT I-III and reduces pigmentation in SPT IV-VI caused by VL+UVA1. AO may help prevent worsening of pigmentary disorders and should be incorporated into photoprotection.
评估了局部抗氧化剂 (AOs) 对可见光加长波紫外线 A1(VL+UVA1)引起的皮肤变化的作用。20 名皮肤光型(SPT)I-VI 的受试者将安慰剂和 AO 混合物的浓度涂抹于背部(AO 0.5%、1.0%和 2.0%)。处理和对照部位用 VL+UVA1 照射。在照射后立即、24 小时和 7 天进行比色和漫反射光谱(DRS)评估。SPT I-III 的受试者出现红斑,24 小时内消退,而 SPT IV-VI 的受试者出现持续性色素沉着。SPT I-III 在 2%AO 部位的红斑明显减少,而 SPT IV-VI 在 2%AO 部位的即刻色素沉着和色素沉着减少(接近显著性,P=0.07)在第 7 天与对照相比。在 24 小时时,从 2%AO 和安慰剂的活检进行免疫组织化学染色,对于任何 SPT 均未显示 COX-2 或 MART-1 的明显变化。对于 SPT IV-VI,细胞周期蛋白 D1 减少,接近显著性(P=0.06),但对于 SPT I-III 则没有。结果表明,局部 AO 可抑制 SPT I-III 的红斑,并减少 VL+UVA1 引起的 SPT IV-VI 的色素沉着。AO 可能有助于预防色素障碍的恶化,应纳入光保护。