烟酰胺
体外
黑素细胞
色素沉着
黑色素
化学
药理学
功能(生物学)
生物化学
癌症研究
皮肤当量
细胞生物学
医学
体外毒理学
细胞毒性
皮肤色素沉着
药品
调制(音乐)
作者
Tomohiro Hakozaki,Timothy Laughlin,Wenzhu Zhao,Gang Deng,Jiazhen Wang,Laurie Moulton
摘要
OBJECTIVE: Niacinamide is a well-established ingredient known for reducing hyperpigmentation by inhibiting melanosome transfer from melanocytes to keratinocytes. This study aimed to explore the potential synergistic effects of niacinamide and low pH in melanogenesis pathways and their impact on skin hyperpigmentation in clinical trials. METHODS: In vitro experiments were conducted using human melanocyte and/or keratinocyte cultures to investigate the effects of niacinamide at varying pH levels (neutral pH 7 and low pH 2.5-4). Melanin synthesis, melanocyte dendricity, melanosome transfer and melanosome degradation were assessed. Transcriptome analysis was performed to identify gene expression changes in human melanocytes. Additionally, vehicle-controlled facial clinical trials were conducted among Caucasian and Chinese females to evaluate the effects of niacinamide formulations at neutral and low pH. RESULTS: Niacinamide in neutral pH solutions and simple low pH solutions (without niacinamide) did not inhibit melanin synthesis or melanocyte dendricity, as expected. However, niacinamide in low pH solutions significantly inhibited both, indicating a synergistic interaction. Enhanced suppression of melanosome transfer and degradation was also observed, although these effects appeared to be additive to the effects of neutral pH niacinamide. Transcriptome analysis revealed downregulation of genes and pathways associated with melanogenic cytokine signalling, melanin biosynthesis, melanocyte dendricity and melanosome transfer for niacinamide in low pH formulation, but not niacinamide in neutral pH or simple low pH formulations (without niacinamide), further supporting the synergistic effect. A 4-week clinical trial among Caucasian females using 2% niacinamide formulation at pH 2.5 revealed a marked reduction in the appearance of facial spots compared to 2% niacinamide neutral pH or vehicle formulations. Similarly, an 8-week clinical trial conducted with Chinese females using 5% niacinamide formulation at pH 4 demonstrated significantly greater efficacy in both facial spot reduction and skin brightening in appearance than neutral pH niacinamide and vehicle formulations. CONCLUSION: Our series of in vitro and clinical studies revealed groundbreaking findings on the role of pH modulation in enhancing the efficacy of niacinamide for hyperpigmentation reduction. By elucidating the synergistic mechanisms involved, this research paves the way for developing more effective treatments aimed at achieving a brighter and more uniform complexion safely.
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