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Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood
In therapeutic interventions associated with melanin hyperpigmentation, tyrosinase is regarded as a target enzyme as it catalyzes the rate-limiting steps in mammalian melanogenesis. Since many known agents have been proven to be toxic, there has been increasing impetus to identify alternative tyrosi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154579/ https://www.ncbi.nlm.nih.gov/pubmed/28333105 http://dx.doi.org/10.3390/molecules22040514 |
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author | Chaita, Eliza Lambrinidis, George Cheimonidi, Christina Agalou, Adamantia Beis, Dimitris Trougakos, Ioannis Mikros, Emmanuel Skaltsounis, Alexios-Leandros Aligiannis, Nektarios |
author_facet | Chaita, Eliza Lambrinidis, George Cheimonidi, Christina Agalou, Adamantia Beis, Dimitris Trougakos, Ioannis Mikros, Emmanuel Skaltsounis, Alexios-Leandros Aligiannis, Nektarios |
author_sort | Chaita, Eliza |
collection | PubMed |
description | In therapeutic interventions associated with melanin hyperpigmentation, tyrosinase is regarded as a target enzyme as it catalyzes the rate-limiting steps in mammalian melanogenesis. Since many known agents have been proven to be toxic, there has been increasing impetus to identify alternative tyrosinase inhibitors, especially from natural sources. In this study, we investigated 900 extracts from Greek plants for potential tyrosinase inhibitive properties. Among the five most potent extracts, the methanol extract of Morus alba wood (MAM) demonstrated a significant reduction in intracellular tyrosinase and melanin content in B16F10 melanoma cells. Bioassay-guided isolation led to the acquisition of twelve compounds: oxyresveratrol (1), kuwanon C (2), mulberroside A (3), resorcinol (4), dihydrooxyresveratol (5), trans-dihydromorin (6), 2,4,3′-trihydroxydihydrostilbene (7), kuwanon H (8), 2,4-dihydroxybenzaldehyde (9), morusin (10), moracin M (11) and kuwanon G (12). Among these, 2,4,3′-trihydroxydihydrostilbene (7) is isolated for the first time from Morus alba and constitutes a novel potent tyrosinase inhibitor (IC(50) 0.8 ± 0.15). We report here for the first time dihydrooxyresveratrol (5) as a potent natural tyrosinase inhibitor (IC(50) 0.3 ± 0.05). Computational docking analysis indicated the binding modes of six tyrosinase inhibitors with the aminoacids of the active centre of tyrosinase. Finally, we found both MAM extract and compounds 1, 6 and 7 to significantly suppress in vivo melanogenesis during zebrafish embryogenesis. |
format | Online Article Text |
id | pubmed-6154579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61545792018-11-13 Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood Chaita, Eliza Lambrinidis, George Cheimonidi, Christina Agalou, Adamantia Beis, Dimitris Trougakos, Ioannis Mikros, Emmanuel Skaltsounis, Alexios-Leandros Aligiannis, Nektarios Molecules Article In therapeutic interventions associated with melanin hyperpigmentation, tyrosinase is regarded as a target enzyme as it catalyzes the rate-limiting steps in mammalian melanogenesis. Since many known agents have been proven to be toxic, there has been increasing impetus to identify alternative tyrosinase inhibitors, especially from natural sources. In this study, we investigated 900 extracts from Greek plants for potential tyrosinase inhibitive properties. Among the five most potent extracts, the methanol extract of Morus alba wood (MAM) demonstrated a significant reduction in intracellular tyrosinase and melanin content in B16F10 melanoma cells. Bioassay-guided isolation led to the acquisition of twelve compounds: oxyresveratrol (1), kuwanon C (2), mulberroside A (3), resorcinol (4), dihydrooxyresveratol (5), trans-dihydromorin (6), 2,4,3′-trihydroxydihydrostilbene (7), kuwanon H (8), 2,4-dihydroxybenzaldehyde (9), morusin (10), moracin M (11) and kuwanon G (12). Among these, 2,4,3′-trihydroxydihydrostilbene (7) is isolated for the first time from Morus alba and constitutes a novel potent tyrosinase inhibitor (IC(50) 0.8 ± 0.15). We report here for the first time dihydrooxyresveratrol (5) as a potent natural tyrosinase inhibitor (IC(50) 0.3 ± 0.05). Computational docking analysis indicated the binding modes of six tyrosinase inhibitors with the aminoacids of the active centre of tyrosinase. Finally, we found both MAM extract and compounds 1, 6 and 7 to significantly suppress in vivo melanogenesis during zebrafish embryogenesis. MDPI 2017-03-23 /pmc/articles/PMC6154579/ /pubmed/28333105 http://dx.doi.org/10.3390/molecules22040514 Text en © 2017 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chaita, Eliza Lambrinidis, George Cheimonidi, Christina Agalou, Adamantia Beis, Dimitris Trougakos, Ioannis Mikros, Emmanuel Skaltsounis, Alexios-Leandros Aligiannis, Nektarios Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title | Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title_full | Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title_fullStr | Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title_full_unstemmed | Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title_short | Anti-Melanogenic Properties of Greek Plants. A Novel Depigmenting Agent from Morus alba Wood |
title_sort | anti-melanogenic properties of greek plants. a novel depigmenting agent from morus alba wood |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154579/ https://www.ncbi.nlm.nih.gov/pubmed/28333105 http://dx.doi.org/10.3390/molecules22040514 |
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