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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
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.
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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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