Suppr超能文献

4-(苯硫基)丁-2-酮在体内外均可抑制黑色素合成及黑素小体成熟。

4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo.

作者信息

Wu Shing-Yi Sean, Wang Hui-Min David, Wen Yi-Shan, Liu Wangta, Li Pin-Hui, Chiu Chien-Chih, Chen Pei-Chin, Huang Chiung-Yao, Sheu Jyh-Horng, Wen Zhi-Hong

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-Sen University, Kaohsiung 804, Taiwan, ROC.

Department of Fragrance and Cosmetic Science, Kaohsiung Medical University, Kaohsiung 807, Taiwan, ROC.

出版信息

Int J Mol Sci. 2015 Aug 26;16(9):20240-57. doi: 10.3390/ijms160920240.

Abstract

In this study, we screened compounds with skin whitening properties and favorable safety profiles from a series of marine related natural products, which were isolated from Formosan soft coral Cladiella australis. Our results indicated that 4-(phenylsulfanyl)butan-2-one could successfully inhibit pigment generation processes in mushroom tyrosinase platform assay, probably through the suppression of tyrosinase activity to be a non-competitive inhibitor of tyrosinase. In cell-based viability examinations, it demonstrated low cytotoxicity on melanoma cells and other normal human cells. It exhibited stronger inhibitions of melanin production and tyrosinase activity than arbutin or 1-phenyl-2-thiourea (PTU). Also, we discovered that 4-(phenylsulfanyl)butan-2-one reduces the protein expressions of melanin synthesis-related proteins, including the microphthalmia-associated transcription factor (MITF), tyrosinase-related protein-1 (Trp-1), dopachrome tautomerase (DCT, Trp-2), and glycoprotein 100 (GP100). In an in vivo zebrafish model, it presented a remarkable suppression in melanogenesis after 48 h. In summary, our in vitro and in vivo biological assays showed that 4-(phenylsulfanyl)butan-2-one possesses anti-melanogenic properties that are significant in medical cosmetology.

摘要

在本研究中,我们从一系列与海洋相关的天然产物中筛选出具有美白特性且安全性良好的化合物,这些天然产物是从台湾软珊瑚澳大利亚扁指软珊瑚中分离得到的。我们的结果表明,4-(苯硫基)丁-2-酮在蘑菇酪氨酸酶平台试验中能够成功抑制色素生成过程,可能是通过抑制酪氨酸酶活性,成为酪氨酸酶的非竞争性抑制剂。在基于细胞的活力检测中,它对黑色素瘤细胞和其他正常人类细胞显示出低细胞毒性。它对黑色素生成和酪氨酸酶活性的抑制作用比熊果苷或1-苯基-2-硫脲(PTU)更强。此外,我们发现4-(苯硫基)丁-2-酮降低了黑色素合成相关蛋白的表达,包括小眼畸形相关转录因子(MITF)、酪氨酸酶相关蛋白-1(Trp-1)、多巴色素互变异构酶(DCT,Trp-2)和糖蛋白100(GP100)。在体内斑马鱼模型中,48小时后它对黑色素生成表现出显著的抑制作用。总之,我们的体外和体内生物学检测表明,4-(苯硫基)丁-2-酮具有抗黑色素生成特性,在医学美容方面具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b58/4613201/4f1a9bf74e72/ijms-16-20240-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验