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Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids

A series of five naturally occurring oxyprenylated phenylpropanoids, namely, the coumarins auraptene (7-geranyloxycoumarin) 1 and 7-isopentenyloxycoumarin 2, and the coumaric acid and ferulic acid derivatives, 4’-isopentenyloxycoumaric acid 3, boropinic acid 4, and 4’-geranyloxyferulic acid 5 were t...

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Autores principales: Epifano, Francesco, Genovese, Salvatore, Palumbo, Lucia, Collevecchio, Chiara, Fiorito, Serena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952183/
https://www.ncbi.nlm.nih.gov/pubmed/36829818
http://dx.doi.org/10.3390/antiox12020259
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author Epifano, Francesco
Genovese, Salvatore
Palumbo, Lucia
Collevecchio, Chiara
Fiorito, Serena
author_facet Epifano, Francesco
Genovese, Salvatore
Palumbo, Lucia
Collevecchio, Chiara
Fiorito, Serena
author_sort Epifano, Francesco
collection PubMed
description A series of five naturally occurring oxyprenylated phenylpropanoids, namely, the coumarins auraptene (7-geranyloxycoumarin) 1 and 7-isopentenyloxycoumarin 2, and the coumaric acid and ferulic acid derivatives, 4’-isopentenyloxycoumaric acid 3, boropinic acid 4, and 4’-geranyloxyferulic acid 5 were tested for their effects on mitochondrial functionality using the organophosphate pesticides glyphosate and chlorpyrifos, and resveratrol, as the reference. While not showing an appreciable in vitro antioxidant activity, and virtually no or a little effect on the viability of non-cancer cell lines BEAS-2B and SHSY-5Y, all phytochemicals exhibited a marked protective effect on mitochondrial potential and activity, with values that were comparable to resveratrol. Auraptene 1 and 7-isopentenyloxycoumarin 2 were seen to be the most effective secondary metabolite to this concern, in particular in being able to completely abolish the decrease of mitochondrial potential induced by increasing concentration of both glyphosate and chlorpyrifos. All the compounds tested also exhibited a protective effect on mitochondrial activity. The potency displayed will shed more light on the molecular basis of the beneficial effects of auraptene, 7-isopentenyloxycoumarin, and structurally related oxyprenylated phenylpropanoids reported to date in the literature.
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spelling pubmed-99521832023-02-25 Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids Epifano, Francesco Genovese, Salvatore Palumbo, Lucia Collevecchio, Chiara Fiorito, Serena Antioxidants (Basel) Article A series of five naturally occurring oxyprenylated phenylpropanoids, namely, the coumarins auraptene (7-geranyloxycoumarin) 1 and 7-isopentenyloxycoumarin 2, and the coumaric acid and ferulic acid derivatives, 4’-isopentenyloxycoumaric acid 3, boropinic acid 4, and 4’-geranyloxyferulic acid 5 were tested for their effects on mitochondrial functionality using the organophosphate pesticides glyphosate and chlorpyrifos, and resveratrol, as the reference. While not showing an appreciable in vitro antioxidant activity, and virtually no or a little effect on the viability of non-cancer cell lines BEAS-2B and SHSY-5Y, all phytochemicals exhibited a marked protective effect on mitochondrial potential and activity, with values that were comparable to resveratrol. Auraptene 1 and 7-isopentenyloxycoumarin 2 were seen to be the most effective secondary metabolite to this concern, in particular in being able to completely abolish the decrease of mitochondrial potential induced by increasing concentration of both glyphosate and chlorpyrifos. All the compounds tested also exhibited a protective effect on mitochondrial activity. The potency displayed will shed more light on the molecular basis of the beneficial effects of auraptene, 7-isopentenyloxycoumarin, and structurally related oxyprenylated phenylpropanoids reported to date in the literature. MDPI 2023-01-23 /pmc/articles/PMC9952183/ /pubmed/36829818 http://dx.doi.org/10.3390/antiox12020259 Text en © 2023 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
Epifano, Francesco
Genovese, Salvatore
Palumbo, Lucia
Collevecchio, Chiara
Fiorito, Serena
Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title_full Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title_fullStr Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title_full_unstemmed Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title_short Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids
title_sort protection of mitochondrial potential and activity by oxyprenylated phenylpropanoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9952183/
https://www.ncbi.nlm.nih.gov/pubmed/36829818
http://dx.doi.org/10.3390/antiox12020259
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