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Irradiation with 590-nm yellow light-emitting diode light attenuates oxidative stress and modulates UVB-induced change of dermal fibroblasts

Authors
Hong, Ji YeonHan, Hye SungYoun, Ji HyunKim, Hyun-wookRyu, Hyun-SeungPark, Kui Young
Issue Date
Jun-2022
Publisher
WILEY
Keywords
fibroblast; oxidative stress; photoaging; ultraviolet; yellow LED
Citation
EXPERIMENTAL DERMATOLOGY, v.31, no.6, pp 931 - 935
Pages
5
Journal Title
EXPERIMENTAL DERMATOLOGY
Volume
31
Number
6
Start Page
931
End Page
935
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/61661
DOI
10.1111/exd.14542
ISSN
0906-6705
1600-0625
Abstract
Recently, light-emitting diode (LED)-based devices have emerged as effective and safe tools for the treatment of photoaged skin. However, few studies have been conducted to elucidate the underlying mechanism behind the effect on photoageing of LED light. In this study, we induced photoageing of human dermal fibroblasts (HDFs) with Ultraviolet B (UVB) irradiation and evaluated the ability of 590-nm LED radiation to induce recovery from oxidative stress, restore collagen formation and regulate inflammatory changes. Photoageing was induced in cultured human dermal fibroblasts (HDFs) using UVB irradiation of 50 mJ/cm(2). Then, the photoaged HDFs were irradiated with LED using a custom-built 590-nm LED device which emits light with an intensity of 38 mW/cm(2) (irradiated for 900 s with 34.2 J/cm(2) of total energy). LED irradiation significantly attenuated UVB-induced reactive oxygen species generation and UVB-induced phosphorylation of JNK, c-Fos and c-Jun. In addition, the procollagen levels were recovered significantly, and MMP-9 levels were significantly suppressed after LED irradiation. The UVB-induced phosphorylation levels of NF-kappa B and pro-inflammatory enzyme COX-2 also significantly decreased. Our results suggest that 590-nm yellow light irradiation may be an effective and safe anti-oxidative and anti-inflammatory treatment modality for photoaged skin.
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