Yeon Jae Lee, Seul Gi Jang, Min Jeong Ryu, Seung Hee Choi
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引用次数: 0
摘要
烟酰胺腺嘌呤二核苷酸(NAD)是生物体内最重要、最基本的成分之一。目前正在进行的大量研究旨在通过提供各种形式的氧化态 NAD(NAD+),利用其在治疗各种疾病方面的潜力。紫外线辐射(UVR)是最常见的环境暴露因素,但也有许多风险。紫外线辐射会影响表皮,导致晒伤、光过敏、DNA 损伤和某些癌症,尤其是黑色素瘤。研究表明,包括烟酰胺核糖苷(NR)在内的 NAD+ 前体可减少老化黑色素细胞的黑色素生成。在这项研究中,我们使用 NR 来确定黑色素沉着是否会在光刺激后受到抑制。我们发现,用α-黑色素细胞刺激素处理的B16F10细胞暴露于特定剂量的NR后,黑色素生成受到抑制。此外,酪氨酸酶的活性(黑色素生成的关键步骤)也受到了抑制。然而,黑色素生成基因的表达水平并无差异。紫外线 B 直接刺激 HaCaT 细胞,诱导金属蛋白酶 RNA 的表达。用 NR 处理可抑制相应基因的表达并降低细胞毒性。这项研究表明,NR 对色素沉着有抑制作用,并能维持受紫外线影响的皮肤层,因此有可能被用作一种新的美白成分。
Nicotinamide Riboside Ameliorates Hyperpigmentation on Photo-Irradiated Skin
Nicotinamide adenine dinucleotide (NAD) is one of the most important and essential components within an organism. Extensive ongoing research is aimed at harnessing its potential in managing diverse diseases by supplying various forms of NAD in its oxidized state, NAD+. Ultraviolet radiation (UVR) is the most common environmental exposure factor, but also carries many risks. UVR affects the epidermis and contributes to sunburn, photo-allergy, DNA damage, and certain cancers, notably melanoma. Research has shown that NAD+ precursors, including nicotinamide riboside (NR), reduce melanogenesis in aged melanocytes. In this study, we used NR to determine whether melanin hyperpigmentation was suppressed after light stimulation. We found that melanogenesis was inhibited when B16F10 cells treated with α-melanocyte-stimulating hormone were exposed to specific doses of NR. Additionally, tyrosinase activity (a key step in melanin production) was suppressed. However, there was no difference in the expression level of melanogenic genes. Ultraviolet B light directly stimulated HaCaT cells, inducing the RNA expression of metalloproteinases. Treatment with NR suppressed the corresponding gene expression and reduced cytotoxicity. This study demonstrates the possibility of using NR as a new skin-whitening ingredient due to its inhibitory effect on hyperpigmentation and ability to maintain skin layers affected by UVR.