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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-9952183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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