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Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils
BACKGROUND: Several low-molecular-weight phenolic acids are present in the blood of septic patients at high levels. The microbial origin of the most of phenolic acids in the human body was shown previously, but pathophysiological role of the phenolic acids is not clear. Sepsis is associated with the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503878/ https://www.ncbi.nlm.nih.gov/pubmed/23061754 http://dx.doi.org/10.1186/1423-0127-19-89 |
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author | Beloborodova, Natalia Bairamov, Iskander Olenin, Andrei Shubina, Victoria Teplova, Vera Fedotcheva, Nadezhda |
author_facet | Beloborodova, Natalia Bairamov, Iskander Olenin, Andrei Shubina, Victoria Teplova, Vera Fedotcheva, Nadezhda |
author_sort | Beloborodova, Natalia |
collection | PubMed |
description | BACKGROUND: Several low-molecular-weight phenolic acids are present in the blood of septic patients at high levels. The microbial origin of the most of phenolic acids in the human body was shown previously, but pathophysiological role of the phenolic acids is not clear. Sepsis is associated with the excessive production of reactive oxygen species (ROS) in both the circulation and the affected organs. In this work the influence of phenolic acids on ROS production in mitochondria and neutrophils was investigated. METHODS: ROS production in mitochondria and neutrophils was determined by MCLA- and luminol-dependent chemiluminescence. The rate of oxygen consumption by mitochondria was determined polarographically. The difference of electric potentials on the inner mitochondrial membrane was registered using a TPP(+)-selective electrode. The formation of phenolic metabolites in monocultures by the members of the main groups of the anaerobic human microflora and aerobic pathogenic bacteria was investigated by the method of gas chromatography–mass spectrometry. RESULTS: All phenolic acids had impact on mitochondria and neutrophils, the main producers of ROS in tissues and circulation. Phenolic acids (benzoic and cinnamic acids) producing the pro-oxidant effect on mitochondria inhibited ROS formation in neutrophils. Their effect on mitochondria was abolished by dithiothreitol (DTT). Phenyllactate and p-hydroxyphenyllactate decreased ROS production in both mitochondria and neutrophils. Bifidobacteria and lactobacilli produced in vitro considerable amounts of phenyllactic and p-hydroxyphenyllactic acids, Clostridia s. produced great quantities of phenylpropionic and p-hydroxyphenylpropionic acids, p-hydroxyphenylacetic acid was produced by Pseudomonas aeruginosa and Acinetobacter baumanii; and benzoic acid, by Serratia marcescens. CONCLUSIONS: The most potent activators of ROS production in mitochondria are phenolic acids whose effect is mediated via the interaction with thiol groups. Among these are benzoic and cinnamic acids. Some phenolic acids, in particular phenyllactate and p-hydroxyphenyllactate, which decrease ROS production in mitochondria and neutrophils, can play a role of natural antioxidants. The results indicate that low-molecular weight phenolic acids of microbial origin participate in the regulation of the ROS production in both the circulation and tissues, thereby affecting the level of oxidative stress in sepsis. |
format | Online Article Text |
id | pubmed-3503878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35038782012-11-22 Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils Beloborodova, Natalia Bairamov, Iskander Olenin, Andrei Shubina, Victoria Teplova, Vera Fedotcheva, Nadezhda J Biomed Sci Research BACKGROUND: Several low-molecular-weight phenolic acids are present in the blood of septic patients at high levels. The microbial origin of the most of phenolic acids in the human body was shown previously, but pathophysiological role of the phenolic acids is not clear. Sepsis is associated with the excessive production of reactive oxygen species (ROS) in both the circulation and the affected organs. In this work the influence of phenolic acids on ROS production in mitochondria and neutrophils was investigated. METHODS: ROS production in mitochondria and neutrophils was determined by MCLA- and luminol-dependent chemiluminescence. The rate of oxygen consumption by mitochondria was determined polarographically. The difference of electric potentials on the inner mitochondrial membrane was registered using a TPP(+)-selective electrode. The formation of phenolic metabolites in monocultures by the members of the main groups of the anaerobic human microflora and aerobic pathogenic bacteria was investigated by the method of gas chromatography–mass spectrometry. RESULTS: All phenolic acids had impact on mitochondria and neutrophils, the main producers of ROS in tissues and circulation. Phenolic acids (benzoic and cinnamic acids) producing the pro-oxidant effect on mitochondria inhibited ROS formation in neutrophils. Their effect on mitochondria was abolished by dithiothreitol (DTT). Phenyllactate and p-hydroxyphenyllactate decreased ROS production in both mitochondria and neutrophils. Bifidobacteria and lactobacilli produced in vitro considerable amounts of phenyllactic and p-hydroxyphenyllactic acids, Clostridia s. produced great quantities of phenylpropionic and p-hydroxyphenylpropionic acids, p-hydroxyphenylacetic acid was produced by Pseudomonas aeruginosa and Acinetobacter baumanii; and benzoic acid, by Serratia marcescens. CONCLUSIONS: The most potent activators of ROS production in mitochondria are phenolic acids whose effect is mediated via the interaction with thiol groups. Among these are benzoic and cinnamic acids. Some phenolic acids, in particular phenyllactate and p-hydroxyphenyllactate, which decrease ROS production in mitochondria and neutrophils, can play a role of natural antioxidants. The results indicate that low-molecular weight phenolic acids of microbial origin participate in the regulation of the ROS production in both the circulation and tissues, thereby affecting the level of oxidative stress in sepsis. BioMed Central 2012-10-12 /pmc/articles/PMC3503878/ /pubmed/23061754 http://dx.doi.org/10.1186/1423-0127-19-89 Text en Copyright ©2012 Beloborodova et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Beloborodova, Natalia Bairamov, Iskander Olenin, Andrei Shubina, Victoria Teplova, Vera Fedotcheva, Nadezhda Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title | Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title_full | Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title_fullStr | Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title_full_unstemmed | Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title_short | Effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
title_sort | effect of phenolic acids of microbial origin on production of reactive oxygen species in mitochondria and neutrophils |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503878/ https://www.ncbi.nlm.nih.gov/pubmed/23061754 http://dx.doi.org/10.1186/1423-0127-19-89 |
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