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Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests

Melanin is the main pigment of human skin, playing the primary role of protection from ultraviolet radiation. Alteration of the melanin production may lead to hyperpigmentation diseases, with both aesthetic and health consequences. Thus, suppressors of melanogenesis are considered useful tools for m...

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Autores principales: Malaspina, Paola, Catellani, Erica, Burlando, Bruno, Brignole, Daniele, Cornara, Laura, Bazzicalupo, Miriam, Candiani, Simona, Obino, Valentina, De Feo, Vincenzo, Caputo, Lucia, Giordani, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233272/
https://www.ncbi.nlm.nih.gov/pubmed/32461836
http://dx.doi.org/10.7717/peerj.9150
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author Malaspina, Paola
Catellani, Erica
Burlando, Bruno
Brignole, Daniele
Cornara, Laura
Bazzicalupo, Miriam
Candiani, Simona
Obino, Valentina
De Feo, Vincenzo
Caputo, Lucia
Giordani, Paolo
author_facet Malaspina, Paola
Catellani, Erica
Burlando, Bruno
Brignole, Daniele
Cornara, Laura
Bazzicalupo, Miriam
Candiani, Simona
Obino, Valentina
De Feo, Vincenzo
Caputo, Lucia
Giordani, Paolo
author_sort Malaspina, Paola
collection PubMed
description Melanin is the main pigment of human skin, playing the primary role of protection from ultraviolet radiation. Alteration of the melanin production may lead to hyperpigmentation diseases, with both aesthetic and health consequences. Thus, suppressors of melanogenesis are considered useful tools for medical and cosmetic treatments. A great interest is focused on natural sources, aimed at finding safe and quantitatively available depigmenting substances. Lichens are thought to be possible sources of this kind of compounds, as the occurrence of many phenolic molecules suggests possible effects on phenolase enzymes involved in melanin synthesis, like tyrosinase. In this work, we used four lichen species, Cetraria islandica Ach., Flavoparmelia caperata Hale, Letharia vulpina (L.) Hue, and Parmotrema perlatum (Hudson) M. Choisy, to obtain extracts in solvents of increasing polarity, viz. chloroform, chloroform-methanol, methanol, and water. Cell-free, tyrosinase inhibition experiments showed highest inhibition for L. vulpina methanol extract, followed by C. islandica chloroform-methanol one. Comparable results for depigmenting activities were observed by means of in vitro and in vivo systems, such as MeWo melanoma cells and zebrafish larvae. Our study provides first evidence of depigmenting effects of lichen extracts, from tyrosinase inhibition to cell and in vivo models, suggesting that L. vulpina and C. islandica extracts deserve to be further studied for developing skin-whitening products.
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spelling pubmed-72332722020-05-26 Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests Malaspina, Paola Catellani, Erica Burlando, Bruno Brignole, Daniele Cornara, Laura Bazzicalupo, Miriam Candiani, Simona Obino, Valentina De Feo, Vincenzo Caputo, Lucia Giordani, Paolo PeerJ Plant Science Melanin is the main pigment of human skin, playing the primary role of protection from ultraviolet radiation. Alteration of the melanin production may lead to hyperpigmentation diseases, with both aesthetic and health consequences. Thus, suppressors of melanogenesis are considered useful tools for medical and cosmetic treatments. A great interest is focused on natural sources, aimed at finding safe and quantitatively available depigmenting substances. Lichens are thought to be possible sources of this kind of compounds, as the occurrence of many phenolic molecules suggests possible effects on phenolase enzymes involved in melanin synthesis, like tyrosinase. In this work, we used four lichen species, Cetraria islandica Ach., Flavoparmelia caperata Hale, Letharia vulpina (L.) Hue, and Parmotrema perlatum (Hudson) M. Choisy, to obtain extracts in solvents of increasing polarity, viz. chloroform, chloroform-methanol, methanol, and water. Cell-free, tyrosinase inhibition experiments showed highest inhibition for L. vulpina methanol extract, followed by C. islandica chloroform-methanol one. Comparable results for depigmenting activities were observed by means of in vitro and in vivo systems, such as MeWo melanoma cells and zebrafish larvae. Our study provides first evidence of depigmenting effects of lichen extracts, from tyrosinase inhibition to cell and in vivo models, suggesting that L. vulpina and C. islandica extracts deserve to be further studied for developing skin-whitening products. PeerJ Inc. 2020-05-15 /pmc/articles/PMC7233272/ /pubmed/32461836 http://dx.doi.org/10.7717/peerj.9150 Text en ©2020 Malaspina et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Plant Science
Malaspina, Paola
Catellani, Erica
Burlando, Bruno
Brignole, Daniele
Cornara, Laura
Bazzicalupo, Miriam
Candiani, Simona
Obino, Valentina
De Feo, Vincenzo
Caputo, Lucia
Giordani, Paolo
Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title_full Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title_fullStr Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title_full_unstemmed Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title_short Depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
title_sort depigmenting potential of lichen extracts evaluated by in vitro and in vivo tests
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7233272/
https://www.ncbi.nlm.nih.gov/pubmed/32461836
http://dx.doi.org/10.7717/peerj.9150
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