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4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo
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 pi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613201/ https://www.ncbi.nlm.nih.gov/pubmed/26343635 http://dx.doi.org/10.3390/ijms160920240 |
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author | 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 |
author_facet | 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 |
author_sort | Wu, Shing-Yi Sean |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4613201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-46132012015-10-26 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo 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 Int J Mol Sci Article 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. MDPI 2015-08-26 /pmc/articles/PMC4613201/ /pubmed/26343635 http://dx.doi.org/10.3390/ijms160920240 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article 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 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title | 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title_full | 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title_fullStr | 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title_full_unstemmed | 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title_short | 4-(Phenylsulfanyl)butan-2-One Suppresses Melanin Synthesis and Melanosome Maturation In Vitro and In Vivo |
title_sort | 4-(phenylsulfanyl)butan-2-one suppresses melanin synthesis and melanosome maturation in vitro and in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613201/ https://www.ncbi.nlm.nih.gov/pubmed/26343635 http://dx.doi.org/10.3390/ijms160920240 |
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