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Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples

Coenzyme Q(10) (CoQ) treatment monitoring is a matter of debate since CoQ distribution from plasma to blood cells and tissues is not fully understood. We aimed to analyze the CoQ levels in a wide set of human biological samples (plasma, blood mononuclear cells (BMCs), platelets, urinary cells, and s...

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Autores principales: Paredes-Fuentes, Abraham J., Montero, Raquel, Codina, Anna, Jou, Cristina, Fernández, Guerau, Maynou, Joan, Santos-Ocaña, Carlos, Riera, Joan, Navas, Plácido, Drobnic, Franchek, Artuch, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601005/
https://www.ncbi.nlm.nih.gov/pubmed/33066002
http://dx.doi.org/10.3390/antiox9100979
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author Paredes-Fuentes, Abraham J.
Montero, Raquel
Codina, Anna
Jou, Cristina
Fernández, Guerau
Maynou, Joan
Santos-Ocaña, Carlos
Riera, Joan
Navas, Plácido
Drobnic, Franchek
Artuch, Rafael
author_facet Paredes-Fuentes, Abraham J.
Montero, Raquel
Codina, Anna
Jou, Cristina
Fernández, Guerau
Maynou, Joan
Santos-Ocaña, Carlos
Riera, Joan
Navas, Plácido
Drobnic, Franchek
Artuch, Rafael
author_sort Paredes-Fuentes, Abraham J.
collection PubMed
description Coenzyme Q(10) (CoQ) treatment monitoring is a matter of debate since CoQ distribution from plasma to blood cells and tissues is not fully understood. We aimed to analyze the CoQ levels in a wide set of human biological samples (plasma, blood mononuclear cells (BMCs), platelets, urinary cells, and skeletal muscle) from a group of 11 healthy male runners before and after CoQ supplementation. The CoQ content in the different samples was analyzed by HPLC coupled to electrochemical detection. No significant differences were observed in the CoQ levels measured in the BMCs, platelets, and urine after the one-month treatment period. Plasma CoQ (expressed in absolute values and values relative to total cholesterol) significantly increased after CoQ supplementation (p = 0.003 in both cases), and the increase in CoQ in muscle approached significance (p = 0.074). CoQ levels were increased in the plasma of all supplemented subjects, and muscle CoQ levels were increased in 8 out of 10 supplemented subjects. In conclusion, the analysis of CoQ in plasma samples seems to be the best surrogate biomarker for CoQ treatment monitoring. Moreover, oral CoQ administration was effective for increasing muscle CoQ concentrations in most subjects.
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spelling pubmed-76010052020-11-01 Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples Paredes-Fuentes, Abraham J. Montero, Raquel Codina, Anna Jou, Cristina Fernández, Guerau Maynou, Joan Santos-Ocaña, Carlos Riera, Joan Navas, Plácido Drobnic, Franchek Artuch, Rafael Antioxidants (Basel) Communication Coenzyme Q(10) (CoQ) treatment monitoring is a matter of debate since CoQ distribution from plasma to blood cells and tissues is not fully understood. We aimed to analyze the CoQ levels in a wide set of human biological samples (plasma, blood mononuclear cells (BMCs), platelets, urinary cells, and skeletal muscle) from a group of 11 healthy male runners before and after CoQ supplementation. The CoQ content in the different samples was analyzed by HPLC coupled to electrochemical detection. No significant differences were observed in the CoQ levels measured in the BMCs, platelets, and urine after the one-month treatment period. Plasma CoQ (expressed in absolute values and values relative to total cholesterol) significantly increased after CoQ supplementation (p = 0.003 in both cases), and the increase in CoQ in muscle approached significance (p = 0.074). CoQ levels were increased in the plasma of all supplemented subjects, and muscle CoQ levels were increased in 8 out of 10 supplemented subjects. In conclusion, the analysis of CoQ in plasma samples seems to be the best surrogate biomarker for CoQ treatment monitoring. Moreover, oral CoQ administration was effective for increasing muscle CoQ concentrations in most subjects. MDPI 2020-10-13 /pmc/articles/PMC7601005/ /pubmed/33066002 http://dx.doi.org/10.3390/antiox9100979 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 Communication
Paredes-Fuentes, Abraham J.
Montero, Raquel
Codina, Anna
Jou, Cristina
Fernández, Guerau
Maynou, Joan
Santos-Ocaña, Carlos
Riera, Joan
Navas, Plácido
Drobnic, Franchek
Artuch, Rafael
Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title_full Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title_fullStr Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title_full_unstemmed Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title_short Coenzyme Q(10) Treatment Monitoring in Different Human Biological Samples
title_sort coenzyme q(10) treatment monitoring in different human biological samples
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601005/
https://www.ncbi.nlm.nih.gov/pubmed/33066002
http://dx.doi.org/10.3390/antiox9100979
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