590nm 发光二极管照射联合活性物质调节紫外线 B 辐射诱导的角质形成细胞炎症。
Light-emitting diode irradiation at 590 nm combined with active substances modulates ultraviolet B radiation-induced keratinocyte inflammation.
机构信息
Flossom Research Laboratories, 2601 Yingfeng Center, 3378 Binhai Avenue, Yuehai Street, Shenzhen, Guangdong, China.
Shenzhen Rawskin Dermatology, Shenzhen, China.
出版信息
Lasers Med Sci. 2024 Sep 3;39(1):231. doi: 10.1007/s10103-024-04178-w.
To evaluate the efficacy of yellow light-emitting diode (LED) irradiation at 590 nm, alone or in combination with anti-inflammatory active substances against ultraviolet (UV)-induced inflammation in keratinocytes. HaCaT keratinocytes were pretreated with LED yellow light (590 nm) alone or in combination with an antiinflammatory active substance such as glycerophosphoinositol choline (GC), extract of grains of paradise (Aframomum melegueta Schum, AM), or a bisabolol and ginger root extract mixture (Bb-GE) before UVB irradiation. Following each treatment, we measured the levels of inflammatory mediators secreted by keratinocytes. HaCaT keratinocytes treated with UVB (300 mJ cm²) and then cultured for 24 h exhibited significantly upregulated expression of proinflammatory factors, including interleukin (IL)-1α, prostaglandin E2 (PGE2), and IL-8. After pretreatment with 590 nm LED, UVB-induced inflammatory responses were significantly inhibited. Co-pretreatment with 590 nm LED irradiation and GC further inhibited the expression of IL-1α and IL-8. IL-8 expression was inhibited by co-pretreatment with 590 nm LED irradiation and AM, whereas PGE2 expression was inhibited by co-pretreatment with 590 nm LED irradiation and Bb-GE. Co-treatment with 590 nm LED irradiation and various active substances modulated UVB-induced inflammation in keratinocytes, suggesting the potential application of this approach to prevent damage caused by voluntary sun exposure in daily life.
为了评估 590nm 黄色发光二极管(LED)单独或与抗炎活性物质联合对角质细胞中紫外线(UV)诱导的炎症的疗效。HaCaT 角质细胞在 UVB 照射前先用 LED 黄色光(590nm)单独或与抗炎活性物质如甘油磷酸胆碱(GC)、天堂谷物提取物(Aframomum melegueta Schum,AM)或 bisabolol 和姜根提取物混合物(Bb-GE)预处理。每种处理后,我们测量角质细胞分泌的炎症介质水平。用 UVB(300mJ/cm²)处理并培养 24 小时的 HaCaT 角质细胞表现出促炎因子的表达显著上调,包括白细胞介素(IL)-1α、前列腺素 E2(PGE2)和 IL-8。用 590nm LED 预处理后,UVB 诱导的炎症反应显著受到抑制。590nm LED 照射与 GC 的共同预处理进一步抑制了 IL-1α 和 IL-8 的表达。590nm LED 照射与 AM 的共同预处理抑制了 IL-8 的表达,而 590nm LED 照射与 Bb-GE 的共同预处理抑制了 PGE2 的表达。590nm LED 照射与各种活性物质的共同处理调节了角质细胞中的 UVB 诱导的炎症,表明这种方法在日常生活中预防自愿日晒引起的损伤具有潜在应用价值。