2022
DOI: 10.3390/antiox11112293
|View full text |Cite
|
Sign up to set email alerts
|

Coenzyme Q10: Role in Less Common Age-Related Disorders

Abstract: In this article we have reviewed the potential role of coenzyme Q10 (CoQ10) in the pathogenesis and treatment of a number of less common age-related disorders, for many of which effective therapies are not currently available. For most of these disorders, mitochondrial dysfunction, oxidative stress and inflammation have been implicated in the disease process, providing a rationale for the potential therapeutic use of CoQ10, because of its key roles in mitochondrial function, as an antioxidant, and as an anti-i… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 116 publications
(122 reference statements)
0
2
0
Order By: Relevance
“…COQ2 produces the enzyme coenzyme-Q2-polyprenyltransferase in the biosynthesis of coenzyme Q 10 , which serves to transport electrons from complexes I and II to complex III [ 32 ]. Deficits in coenzyme Q 10 impair oxidative phosphorylation and enhance the vulnerability of cells to harm by free radicals [ 32 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…COQ2 produces the enzyme coenzyme-Q2-polyprenyltransferase in the biosynthesis of coenzyme Q 10 , which serves to transport electrons from complexes I and II to complex III [ 32 ]. Deficits in coenzyme Q 10 impair oxidative phosphorylation and enhance the vulnerability of cells to harm by free radicals [ 32 ].…”
Section: Resultsmentioning
confidence: 99%
“…COQ2 produces the enzyme coenzyme-Q2-polyprenyltransferase in the biosynthesis of coenzyme Q 10 , which serves to transport electrons from complexes I and II to complex III [ 32 ]. Deficits in coenzyme Q 10 impair oxidative phosphorylation and enhance the vulnerability of cells to harm by free radicals [ 32 ]. In a recent meta-analysis, V393A was shown to be a susceptibility variant instead of causative for MSA (specifically, MSA-C) in East Asian cohorts [ 33 ].…”
Section: Resultsmentioning
confidence: 99%