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用局部抗氧化剂减轻可见光和长波 UVA1 引起的作用。

Mitigating Visible Light and Long Wavelength UVA1-induced Effects with Topical Antioxidants.

机构信息

Photomedicine and Photobiology Unit, Department of Dermatology, Henry Ford Hospital, Detroit, MI.

Graduate Medical Education, Broward Health Medical Center, Fort Lauderdale, FL.

出版信息

Photochem Photobiol. 2022 Mar;98(2):455-460. doi: 10.1111/php.13525. Epub 2021 Oct 4.

Abstract

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.

摘要

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。

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