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Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach

Targeting antioxidants to mitochondria is considered a promising strategy to prevent cellular senescence and skin ageing. In this study, we investigate whether four hydroxybenzoic acid-based mitochondria-targeted antioxidants (MitoBENs, MB1-4) could be used as potential active ingredients to prevent...

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Autores principales: Fernandes, Carlos, Cagide, Fernando, Simões, Jorge, Pita, Carlos, Pereira, Eurico, Videira, Afonso J. C., Soares, Pedro, Duarte, José F. S., Santos, António M. S., Oliveira, Paulo J., Borges, Fernanda, Silva, Filomena S. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571003/
https://www.ncbi.nlm.nih.gov/pubmed/36234718
http://dx.doi.org/10.3390/molecules27196183
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author Fernandes, Carlos
Cagide, Fernando
Simões, Jorge
Pita, Carlos
Pereira, Eurico
Videira, Afonso J. C.
Soares, Pedro
Duarte, José F. S.
Santos, António M. S.
Oliveira, Paulo J.
Borges, Fernanda
Silva, Filomena S. G.
author_facet Fernandes, Carlos
Cagide, Fernando
Simões, Jorge
Pita, Carlos
Pereira, Eurico
Videira, Afonso J. C.
Soares, Pedro
Duarte, José F. S.
Santos, António M. S.
Oliveira, Paulo J.
Borges, Fernanda
Silva, Filomena S. G.
author_sort Fernandes, Carlos
collection PubMed
description Targeting antioxidants to mitochondria is considered a promising strategy to prevent cellular senescence and skin ageing. In this study, we investigate whether four hydroxybenzoic acid-based mitochondria-targeted antioxidants (MitoBENs, MB1-4) could be used as potential active ingredients to prevent senescence in skin cells. Firstly, we evaluated the chemical stability, cytotoxicity, genotoxicity and mitochondrial toxicity of all compounds. We followed this by testing the antioxidant protective capacity of the two less toxic compounds on human skin fibroblasts. We then assessed the effects of the best hit on senescence, inflammation and mitochondrial remodeling on a 3D skin cell model, while also testing its mutagenic potential. Cytotoxicity and mitochondrial toxicity rankings were produced: MB3 < MB4 ≃ MB1 < MB2 and MB3 < MB1 < MB4 < MB2, respectively. These results suggest that pyrogallol-based compounds (MB2 and MB4) have lower cytotoxicity. The pyrogallol derivative, MB2, containing a 6-carbon spacer, showed a more potent antioxidant protective activity against hydrogen peroxide cytotoxicity. In a 3D skin cell model, MB2 also decreased transcripts related to senescence. In sum, MB2’s biological safety profile, good chemical stability and lack of mutagenicity, combined with its anti-senescence effect, converts MB2 into a good candidate for further development as an active ingredient for skin anti-ageing products.
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spelling pubmed-95710032022-10-17 Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach Fernandes, Carlos Cagide, Fernando Simões, Jorge Pita, Carlos Pereira, Eurico Videira, Afonso J. C. Soares, Pedro Duarte, José F. S. Santos, António M. S. Oliveira, Paulo J. Borges, Fernanda Silva, Filomena S. G. Molecules Article Targeting antioxidants to mitochondria is considered a promising strategy to prevent cellular senescence and skin ageing. In this study, we investigate whether four hydroxybenzoic acid-based mitochondria-targeted antioxidants (MitoBENs, MB1-4) could be used as potential active ingredients to prevent senescence in skin cells. Firstly, we evaluated the chemical stability, cytotoxicity, genotoxicity and mitochondrial toxicity of all compounds. We followed this by testing the antioxidant protective capacity of the two less toxic compounds on human skin fibroblasts. We then assessed the effects of the best hit on senescence, inflammation and mitochondrial remodeling on a 3D skin cell model, while also testing its mutagenic potential. Cytotoxicity and mitochondrial toxicity rankings were produced: MB3 < MB4 ≃ MB1 < MB2 and MB3 < MB1 < MB4 < MB2, respectively. These results suggest that pyrogallol-based compounds (MB2 and MB4) have lower cytotoxicity. The pyrogallol derivative, MB2, containing a 6-carbon spacer, showed a more potent antioxidant protective activity against hydrogen peroxide cytotoxicity. In a 3D skin cell model, MB2 also decreased transcripts related to senescence. In sum, MB2’s biological safety profile, good chemical stability and lack of mutagenicity, combined with its anti-senescence effect, converts MB2 into a good candidate for further development as an active ingredient for skin anti-ageing products. MDPI 2022-09-21 /pmc/articles/PMC9571003/ /pubmed/36234718 http://dx.doi.org/10.3390/molecules27196183 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fernandes, Carlos
Cagide, Fernando
Simões, Jorge
Pita, Carlos
Pereira, Eurico
Videira, Afonso J. C.
Soares, Pedro
Duarte, José F. S.
Santos, António M. S.
Oliveira, Paulo J.
Borges, Fernanda
Silva, Filomena S. G.
Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title_full Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title_fullStr Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title_full_unstemmed Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title_short Targeting Hydroxybenzoic Acids to Mitochondria as a Strategy to Delay Skin Ageing: An In Vitro Approach
title_sort targeting hydroxybenzoic acids to mitochondria as a strategy to delay skin ageing: an in vitro approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571003/
https://www.ncbi.nlm.nih.gov/pubmed/36234718
http://dx.doi.org/10.3390/molecules27196183
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