Literature DB >> 25126052

Coenzyme q10 therapy.

Juan Garrido-Maraver1, Mario D Cordero2, Manuel Oropesa-Ávila1, Alejandro Fernández Vega1, Mario de la Mata1, Ana Delgado Pavón1, Manuel de Miguel3, Carmen Pérez Calero1, Marina Villanueva Paz1, David Cotán1, José A Sánchez-Alcázar4.   

Abstract

For a number of years, coenzyme Q10 (CoQ10) 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 CoQ10. Also, at the inner mitochondrial membrane level, CoQ10 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 CoQ10 affects the expression of genes involved in human cell signaling, metabolism and transport, and some of the effects of CoQ10 supplementation may be due to this property. CoQ10 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 CoQ10 levels as well as different ataxias and encephalomyopathies. CoQ10 treatment does not cause serious adverse effects in humans and new formulations have been developed that increase CoQ10 absorption and tissue distribution. Oral administration of CoQ10 is a frequent antioxidant strategy in many diseases that may provide a significant symptomatic benefit.

Entities:  

Keywords:  Clinical indications; Coenzyme Q10; Coenzyme Q10-related compounds; Pharmacokinetics

Year:  2014        PMID: 25126052      PMCID: PMC4112525          DOI: 10.1159/000360101

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  126 in total

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