Irradiation of Skin with Visible Light Induces Reactive Oxygen Species and Matrix-Degrading Enzymes

• Published in: Journal of investigative dermatology Vol. 132; no. 7; pp. 1901 - 1907
• Main Authors: Liebel, Frank, Kaur, Simarna, Ruvolo, Eduardo, Kollias, Nikiforos, Southall, Michael D.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.07.2012; Nature Publishing Group; Elsevier Limited
• Subjects: Antioxidants - pharmacology; Biological and medical sciences; Cells, Cultured; Cytokines - biosynthesis; Dermatology; Extracellular Signal-Regulated MAP Kinases - physiology; Humans; Light; Luminescent Measurements; Matrix Metalloproteinases - biosynthesis; Medical sciences; Pyrimidine Dimers - biosynthesis; Reactive Oxygen Species - metabolism; Receptor, Epidermal Growth Factor - physiology; Signal Transduction - radiation effects; Skin - metabolism; Skin - radiation effects; Ultraviolet Rays; Oxygen; Skin; Dermatology; Free radical
• ISSN: 0022-202X; 1523-1747; 1523-1747
• DOI: 10.1038/jid.2011.476

Daily skin exposure to solar radiation causes cells to produce reactive oxygen species (ROS), which are a primary factor in skin damage. Although the contribution of the UV component to skin damage has been established, few studies have examined the effects of non-UV solar radiation on skin physiology. Solar radiation comprises <10% of UV, and thus the purpose of this study was to examine the physiological response of skin to visible light (400–700nm). Irradiation of human skin equivalents with visible light induced production of ROS, proinflammatory cytokines, and matrix metalloproteinase (MMP)-1 expression. Commercially available sunscreens were found to have minimal effects on reducing visible light–induced ROS, suggesting that UVA/UVB sunscreens do not protect the skin from visible light–induced responses. Using clinical models to assess the generation of free radicals from oxidative stress, higher levels of free radical activity were found after visible light exposure. Pretreatment with a photostable UVA/UVB sunscreen containing an antioxidant combination significantly reduced the production of ROS, cytokines, and MMP expression in vitro, and decreased oxidative stress in human subjects after visible light irradiation. Taken together, these findings suggest that other portions of the solar spectrum aside from UV, particularly visible light, may also contribute to signs of premature photoaging in skin.