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AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects
Taking advantage of Light Up Cell System (LUCS) technology, which allows for fine monitoring of reactive oxygen species (ROS) production inside live cells, a new assay called Anti Oxidant Power 1 (AOP1) was developed to specifically measure ROS and/or free-radical scavenging effects inside living ce...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346189/ https://www.ncbi.nlm.nih.gov/pubmed/32492957 http://dx.doi.org/10.3390/antiox9060471 |
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author | Gironde, Camille Rigal, Mylène Dufour, Cécile Furger, Christophe |
author_facet | Gironde, Camille Rigal, Mylène Dufour, Cécile Furger, Christophe |
author_sort | Gironde, Camille |
collection | PubMed |
description | Taking advantage of Light Up Cell System (LUCS) technology, which allows for fine monitoring of reactive oxygen species (ROS) production inside live cells, a new assay called Anti Oxidant Power 1 (AOP1) was developed to specifically measure ROS and/or free-radical scavenging effects inside living cells. This method is quantitative and EC(50)s obtained from AOP1 dose-response experiments were determined in order to classify the intracellular antioxidant efficacy of 15 well known antioxidant compounds with different hydrophilic properties. Six of them (epigallocatechin gallate, quercetin, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), ethoxyquin, resveratrol) gave EC(50)s in the range of 7–64 μM, four (Trolox, catechin, epicatechin, EUK134) in the range of 0.14 to 1 mM, and 5 (sulforaphane, astaxanthin, α- and γ-tocopherols, vitamin E acetate) showed only partial or no effect. Interestingly, effects with measurable EC(50)s were observed for compounds with hydrophilic properties (LogP ≤ 5.3), while all antioxidants known to act at the plasma membrane level (LogP ≥ 10.3) had partial or no effect. Sulforaphane, a hydrophilic but strict Keap1/Nrf2 pathway enhancer, did not show any effect either. Importantly, AOP1 assay captures both antioxidant and prooxidant effects. Taken together, these results led us to the conclusion that AOP1 assay measures antioxidant effect of compounds that selectively enter the cell, and act as free radical scavengers in the cytosol and/or nucleus level. |
format | Online Article Text |
id | pubmed-7346189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73461892020-07-14 AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects Gironde, Camille Rigal, Mylène Dufour, Cécile Furger, Christophe Antioxidants (Basel) Article Taking advantage of Light Up Cell System (LUCS) technology, which allows for fine monitoring of reactive oxygen species (ROS) production inside live cells, a new assay called Anti Oxidant Power 1 (AOP1) was developed to specifically measure ROS and/or free-radical scavenging effects inside living cells. This method is quantitative and EC(50)s obtained from AOP1 dose-response experiments were determined in order to classify the intracellular antioxidant efficacy of 15 well known antioxidant compounds with different hydrophilic properties. Six of them (epigallocatechin gallate, quercetin, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), ethoxyquin, resveratrol) gave EC(50)s in the range of 7–64 μM, four (Trolox, catechin, epicatechin, EUK134) in the range of 0.14 to 1 mM, and 5 (sulforaphane, astaxanthin, α- and γ-tocopherols, vitamin E acetate) showed only partial or no effect. Interestingly, effects with measurable EC(50)s were observed for compounds with hydrophilic properties (LogP ≤ 5.3), while all antioxidants known to act at the plasma membrane level (LogP ≥ 10.3) had partial or no effect. Sulforaphane, a hydrophilic but strict Keap1/Nrf2 pathway enhancer, did not show any effect either. Importantly, AOP1 assay captures both antioxidant and prooxidant effects. Taken together, these results led us to the conclusion that AOP1 assay measures antioxidant effect of compounds that selectively enter the cell, and act as free radical scavengers in the cytosol and/or nucleus level. MDPI 2020-06-01 /pmc/articles/PMC7346189/ /pubmed/32492957 http://dx.doi.org/10.3390/antiox9060471 Text en © 2020 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 Gironde, Camille Rigal, Mylène Dufour, Cécile Furger, Christophe AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title | AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title_full | AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title_fullStr | AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title_full_unstemmed | AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title_short | AOP1, a New Live Cell Assay for the Direct and Quantitative Measure of Intracellular Antioxidant Effects |
title_sort | aop1, a new live cell assay for the direct and quantitative measure of intracellular antioxidant effects |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346189/ https://www.ncbi.nlm.nih.gov/pubmed/32492957 http://dx.doi.org/10.3390/antiox9060471 |
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