Department of Biochemistry, Chung-Ang University College of Medicine, Seoul 156-756, Korea.
Organic Chemistry Laboratory, Korea Institute of Science & Technology, Seoul 136-791, Korea.
Korean J Physiol Pharmacol. 2014 Jun;18(3):249-54. doi: 10.4196/kjpp.2014.18.3.249. Epub 2014 Jun 12.
The purpose of this study is to characterize the effects of KHG26792 (3-(naphthalen-2-yl(propoxy) methyl)azetidine hydrochloride), a potential skin whitening agent, on melanin synthesis and identify the underlying mechanism of action. Our data showed that KHG26792 significantly reduced melanin synthesis in a dose-dependent manner. Additionally, KHG26792 downregulated microphthalmia-associated transcription factor (MITF) and tyrosinase, the rate-limiting enzyme in melanogenesis, although tyrosinase was not inhibited directly. KHG26792 activated extracellular signal-regulated kinase (ERK), whereas an ERK pathway inhibitor, PD98059, rescued KHG26792-induced hypopigmentation. These results suggest that KHG26792 decreases melanin production via ERK activation. Moreover, the hypopigmentary effects of KHG26792 were confirmed in a pigmented skin equivalent model using Cervi cornus Colla (deer antler glue), in which the color of the pigmented artificial skin became lighter after treatment with KHG26792. In summary, our findings suggest that KHG26792 is a novel skin whitening agent.
本研究旨在探讨 KHG26792(3-(萘-2-基(丙氧基)甲基)氮杂啶盐酸盐)作为一种潜在的皮肤美白剂对黑色素合成的影响,并确定其作用机制。我们的数据表明,KHG26792 可显著降低黑色素的合成,呈剂量依赖性。此外,尽管 KHG26792 不能直接抑制酪氨酸酶,但它可下调小眼畸形相关转录因子(MITF)和黑色素生成中的限速酶酪氨酸酶。KHG26792 激活细胞外信号调节激酶(ERK),而 ERK 通路抑制剂 PD98059 可挽救 KHG26792 诱导的色素减退。这些结果表明,KHG26792 通过激活 ERK 减少黑色素生成。此外,在使用 Cervi cornus Colla(鹿角胶)的色素皮肤等效模型中证实了 KHG26792 的色素减退作用,经 KHG26792 处理后,色素人工皮肤的颜色变浅。综上所述,我们的研究结果表明,KHG26792 是一种新型的皮肤美白剂。