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Coenzyme Q10 Supplementation in Aging and Disease
Coenzyme Q (CoQ) is an essential component of the mitochondrial electron transport chain and an antioxidant in plasma membranes and lipoproteins. It is endogenously produced in all cells by a highly regulated pathway that involves a mitochondrial multiprotein complex. Defects in either the structura...
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Published in: | Frontiers in physiology 2018-02, Vol.9, p.44-44 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Coenzyme Q (CoQ) is an essential component of the mitochondrial electron transport chain and an antioxidant in plasma membranes and lipoproteins. It is endogenously produced in all cells by a highly regulated pathway that involves a mitochondrial multiprotein complex. Defects in either the structural and/or regulatory components of CoQ complex or in non-CoQ biosynthetic mitochondrial proteins can result in a decrease in CoQ concentration and/or an increase in oxidative stress. Besides CoQ
10
deficiency syndrome and aging, there are chronic diseases in which lower levels of CoQ
10
are detected in tissues and organs providing the hypothesis that CoQ
10
supplementation could alleviate aging symptoms and/or retard the onset of these diseases. Here, we review the current knowledge of CoQ
10
biosynthesis and primary CoQ
10
deficiency syndrome, and have collected published results from clinical trials based on CoQ
10
supplementation. There is evidence that supplementation positively affects mitochondrial deficiency syndrome and the symptoms of aging based mainly on improvements in bioenergetics. Cardiovascular disease and inflammation are alleviated by the antioxidant effect of CoQ
10
. There is a need for further studies and clinical trials involving a greater number of participants undergoing longer treatments in order to assess the benefits of CoQ
10
treatment in metabolic syndrome and diabetes, neurodegenerative disorders, kidney diseases, and human fertility. |
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ISSN: | 1664-042X 1664-042X |
DOI: | 10.3389/fphys.2018.00044 |