2021
DOI: 10.1016/j.abd.2020.05.016
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Expression of OPN3 in fibroblasts, melanocytes, and keratinocytes of skin with facial melasma in comparison with unaffected adjacent skin

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Cited by 4 publications
(2 citation statements)
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“…20 Nevertheless, OPN3 receptors were not differentially expressed in keratinocytes, melanocytes, or fibroblasts between facial melasma and the healthy adjacent skin. 21 Visible light-induced hyperpigmentation in darker skin types was deeper and longer-lasting over a two-week period compared to UVA1. 22 In addition, compared with UVB irradiation, blue-violet light (415 nm) induced significantly evident hyperpigmentation in a dose-dependent manner.…”
Section: Ultraviolet and Visible Light Exposurementioning
confidence: 92%
“…20 Nevertheless, OPN3 receptors were not differentially expressed in keratinocytes, melanocytes, or fibroblasts between facial melasma and the healthy adjacent skin. 21 Visible light-induced hyperpigmentation in darker skin types was deeper and longer-lasting over a two-week period compared to UVA1. 22 In addition, compared with UVB irradiation, blue-violet light (415 nm) induced significantly evident hyperpigmentation in a dose-dependent manner.…”
Section: Ultraviolet and Visible Light Exposurementioning
confidence: 92%
“…Pigmentation is found only in darker phototypes (III-VI) after high doses of VL exposure, and only shorter wavelengths (420-470 nm, blue and violet) can induce pigmentation through the activation of opsin 3 (OPN3) receptors in melanocytes [31]. While OPN3 is not overexpressed in skin with facial melasma compared with adjacent skin, use of tinted sunscreens (with iron oxides), which block short VL wavelengths, enhances the depigmenting effect of hydroquinone and hinders melasma pigmentation in summer [32,33].…”
Section: Solar Radiationmentioning
confidence: 99%