Duteil Luc, Cardot-Leccia Nathalie, Queille-Roussel Catherine, Maubert Yves, Harmelin Yona, Boukari Fériel, Ambrosetti Damien, Lacour Jean-Philippe, Passeron Thierry
Centre de Pharmacologie Clinique Appliquée à la Dermatologie (CPCAD), University hospital of Nice, Nice, France.
Pigment Cell Melanoma Res. 2014 Sep;27(5):822-6. doi: 10.1111/pcmr.12273. Epub 2014 Jul 25.
The visible light spectrum is wide, and it can be hypothesized that all the wavelengths between 400-700 nm do not induce the same photobiological effects on pigmentation. We assessed the potential pro-pigmenting effects of two single wavelengths located at both extremities of the visible spectrum: the blue/violet line (λ = 415 nm) and the red line (λ = 630 nm). We made colorimetric, clinical, and histological assessments with increasing doses of those lights on healthy volunteers. Then, we compared these irradiations to non-exposed and UVB-exposed skin. Colorimetric and clinical assessments showed a clear dose effect with the 415-nm irradiation, in both skin type III and IV subjects, whereas the 630 nm did not induce hyperpigmentation. When compared to UVB irradiation, the blue-violet light induced a significantly more pronounced hyperpigmentation that lasted up to 3 months. Histological examination showed a significant increase of keratinocyte necrosis and p53 with UVB, as compared to 415- and 630-nm exposures.
可见光谱范围很广,可以推测400 - 700纳米之间的所有波长对色素沉着不会产生相同的光生物学效应。我们评估了位于可见光谱两端的两个单一波长的潜在促色素沉着作用:蓝/紫线(λ = 415纳米)和红线(λ = 630纳米)。我们对健康志愿者使用递增剂量的这些光进行了比色、临床和组织学评估。然后,我们将这些照射与未照射和紫外线B(UVB)照射的皮肤进行了比较。比色和临床评估显示,在III型和IV型皮肤受试者中,415纳米照射均呈现明显的剂量效应,而630纳米照射未引起色素沉着过度。与UVB照射相比,蓝紫光引起的色素沉着过度明显更显著,且持续长达3个月。组织学检查显示,与415纳米和630纳米照射相比,UVB照射导致角质形成细胞坏死和p53显著增加。