Coenzyme Q(10) Therapy

For a number of years, coenzyme Q 10 (CoQ 10 ) was known for its key role in mitochondrial bioenergetics; later studies demonstrated its presence in other subcellular fractions and in blood plasma, and extensively investigated its antioxidant role. These 2 functions constitute the basis for supporti...

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Autores: Garrido-Maraver, Juan, Cordero, Mario D., Oropesa-Ávila, Manuel, Fernández Vega, Alejandro, Mata, Mario de la, Delgado Pavón, Ana, Miguel Rodríguez, Manuel de, Sánchez-Alcázar, José Antonio
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/142548
Acceso en línea:https://hdl.handle.net/11441/142548
https://doi.org/10.1159/000360101
Access Level:acceso abierto
Palabra clave:Clinical indications
Coenzyme Q 10
Coenzyme Q 10 -related compounds
Pharmacokinetics
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spelling Coenzyme Q(10) TherapyGarrido-Maraver, JuanCordero, Mario D.Oropesa-Ávila, ManuelFernández Vega, AlejandroMata, Mario de laDelgado Pavón, AnaMiguel Rodríguez, Manuel deSánchez-Alcázar, José AntonioClinical indicationsCoenzyme Q 10Coenzyme Q 10 -related compoundsPharmacokineticsFor a number of years, coenzyme Q 10 (CoQ 10 ) was known for its key role in mitochondrial bioenergetics; later studies demonstrated its presence in other subcellular fractions and in blood plasma, and extensively investigated its antioxidant role. These 2 functions constitute the basis for supporting the clinical use of CoQ 10 . Also, at the inner mitochondrial membrane level, CoQ 10 is recognized as an obligatory cofactor for the function of uncoupling proteins and a modulator of the mitochondrial transition pore. Furthermore, recent data indicate that CoQ 10 affects the expression of genes involved in human cell signaling, metabolism and transport, and some of the effects of CoQ 10 supplementation may be due to this property. CoQ 10 deficiencies are due to autosomal recessive mutations, mitochondrial diseases, aging-related oxidative stress and carcinogenesis processes, and also statin treatment. Many neurodegenerative disorders, diabetes, cancer, and muscular and cardiovascular diseases have been associated with low CoQ 10 levels as well as different ataxias and encephalomyopathies. CoQ 10 treatment does not cause serious adverse effects in humans and new formuhave been developed that increase CoQ 10 absorption and tissue distribution. Oral administration of CoQ 10 is a frequent antioxidant strategy in many diseases that may provide a significant symptomatic benefit.KARGERCitología e Histología Normal y PatológicaMinisterio de Sanidad. EspañaServicio Andaluz de Salud. Junta de Andalucía2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/142548https://doi.org/10.1159/000360101reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésMolecular Syndromology, 5 (3-4), 187-197.FIS PI10/00543FIS EC08/00076SAS 111242https://www.karger.com/Article/FullText/360101info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1425482026-06-17T12:51:07Z
dc.title.none.fl_str_mv Coenzyme Q(10) Therapy
title Coenzyme Q(10) Therapy
spellingShingle Coenzyme Q(10) Therapy
Garrido-Maraver, Juan
Clinical indications
Coenzyme Q 10
Coenzyme Q 10 -related compounds
Pharmacokinetics
title_short Coenzyme Q(10) Therapy
title_full Coenzyme Q(10) Therapy
title_fullStr Coenzyme Q(10) Therapy
title_full_unstemmed Coenzyme Q(10) Therapy
title_sort Coenzyme Q(10) Therapy
dc.creator.none.fl_str_mv Garrido-Maraver, Juan
Cordero, Mario D.
Oropesa-Ávila, Manuel
Fernández Vega, Alejandro
Mata, Mario de la
Delgado Pavón, Ana
Miguel Rodríguez, Manuel de
Sánchez-Alcázar, José Antonio
author Garrido-Maraver, Juan
author_facet Garrido-Maraver, Juan
Cordero, Mario D.
Oropesa-Ávila, Manuel
Fernández Vega, Alejandro
Mata, Mario de la
Delgado Pavón, Ana
Miguel Rodríguez, Manuel de
Sánchez-Alcázar, José Antonio
author_role author
author2 Cordero, Mario D.
Oropesa-Ávila, Manuel
Fernández Vega, Alejandro
Mata, Mario de la
Delgado Pavón, Ana
Miguel Rodríguez, Manuel de
Sánchez-Alcázar, José Antonio
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Citología e Histología Normal y Patológica
Ministerio de Sanidad. España
Servicio Andaluz de Salud. Junta de Andalucía
dc.subject.none.fl_str_mv Clinical indications
Coenzyme Q 10
Coenzyme Q 10 -related compounds
Pharmacokinetics
topic Clinical indications
Coenzyme Q 10
Coenzyme Q 10 -related compounds
Pharmacokinetics
description For a number of years, coenzyme Q 10 (CoQ 10 ) was known for its key role in mitochondrial bioenergetics; later studies demonstrated its presence in other subcellular fractions and in blood plasma, and extensively investigated its antioxidant role. These 2 functions constitute the basis for supporting the clinical use of CoQ 10 . Also, at the inner mitochondrial membrane level, CoQ 10 is recognized as an obligatory cofactor for the function of uncoupling proteins and a modulator of the mitochondrial transition pore. Furthermore, recent data indicate that CoQ 10 affects the expression of genes involved in human cell signaling, metabolism and transport, and some of the effects of CoQ 10 supplementation may be due to this property. CoQ 10 deficiencies are due to autosomal recessive mutations, mitochondrial diseases, aging-related oxidative stress and carcinogenesis processes, and also statin treatment. Many neurodegenerative disorders, diabetes, cancer, and muscular and cardiovascular diseases have been associated with low CoQ 10 levels as well as different ataxias and encephalomyopathies. CoQ 10 treatment does not cause serious adverse effects in humans and new formuhave been developed that increase CoQ 10 absorption and tissue distribution. Oral administration of CoQ 10 is a frequent antioxidant strategy in many diseases that may provide a significant symptomatic benefit.
publishDate 2014
dc.date.none.fl_str_mv 2014
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/11441/142548
https://doi.org/10.1159/000360101
url https://hdl.handle.net/11441/142548
https://doi.org/10.1159/000360101
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Molecular Syndromology, 5 (3-4), 187-197.
FIS PI10/00543
FIS EC08/00076
SAS 111242
https://www.karger.com/Article/FullText/360101
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv KARGER
publisher.none.fl_str_mv KARGER
dc.source.none.fl_str_mv reponame:idUS. Depósito de Investigación de la Universidad de Sevilla
instname:Universidad de Sevilla (US)
instname_str Universidad de Sevilla (US)
reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
collection idUS. Depósito de Investigación de la Universidad de Sevilla
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