首页> 美国卫生研究院文献>Scientific Reports >The UV/Visible Radiation Boundary Region (385–405 nm) Damages Skin Cells and Induces dark Cyclobutane Pyrimidine Dimers in Human Skin in vivo
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The UV/Visible Radiation Boundary Region (385–405 nm) Damages Skin Cells and Induces dark Cyclobutane Pyrimidine Dimers in Human Skin in vivo

机译:紫外线/可见辐射边界区域(385–405 nm)会损害皮肤细胞并在体内诱导人体皮肤中的深色环丁烷嘧啶二聚体

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摘要

The adverse effects of terrestrial solar ultraviolet radiation (UVR) (~295–400 nm) on the skin are well documented, especially in the UVB region (~295–320 nm). The effects of very long-wave UVA (>380 nm) and visible radiation (≥400 nm) are much less known. Sunscreens have been beneficial in inhibiting a wide range of photodamage, however most formulations provide very little protection in the long wave UVA region (380–400 nm) and almost none from shortwave visible wavelengths (400–420 nm). We demonstrate photodamage in this region for a number of different endpoints including cell viability, DNA damage (delayed cyclobutane pyrimidine dimers), differential gene expression (for genes associated with inflammation, oxidative stress and photoageing) and induction of oxidizing species in vitro in HaCaT keratinocytes and in vivo in human volunteers. This work has implications for phototherapy and photoprotection.
机译:地面太阳紫外线辐射(UVR)(〜295-400 nm)对皮肤的不利影响已有充分文献记载,尤其是在UVB区(〜295-320 nm)。非常不知道长波UVA(> 380 nm)和可见光(≥400nm)的影响。防晒霜在抑制多种光损伤方面一直是有益的,但是大多数制剂在长波UVA区域(380-400 nm)几乎没有提供保护,而对短波可见光波长(400-420 nm)几乎没有提供保护。我们证明了该区域在许多不同端点的光损伤,包括细胞活力,DNA损伤(环丁烷嘧啶二聚体延迟),差异基因表达(与炎症,氧化应激和光老化相关的基因)以及在HaCaT角质形成细胞中体外诱导的氧化物种。并在人类志愿者体内进行。这项工作对光疗和光保护有影响。

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