Coenzyme Q10 supplementation ameliorates inflammatory signaling and oxidative stress associated with strenuous exercise
Background Exhausting exercise induces muscle damage associated with high production of free radicals and pro-inflammatory mediators. Aim The objective of this study was to determine for the first time and simultaneously whether oral coenzyme Q 10 (CoQ 10 ) supplementation can prevent over-expressio...
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Veröffentlicht in: | European journal of nutrition 2012-10, Vol.51 (7), p.791-799 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background
Exhausting exercise induces muscle damage associated with high production of free radicals and pro-inflammatory mediators.
Aim
The objective of this study was to determine for the first time and simultaneously whether oral coenzyme Q
10
(CoQ
10
) supplementation can prevent over-expression of inflammatory mediators and oxidative stress associated with strenuous exercise.
Methods
The participants were classified in two groups: CoQ
10
group (CG) and placebo group (PG). The physical test consisted in a constant run (50 km) that combined several degrees of high effort (mountain run and ultra-endurance), in permanent climbing.
Results
Exercise was associated with an increase in TNF-α, IL-6, 8-hydroxy-2′-deoxyguanosine (8-OHdG), and isoprostane levels, revealing the degree of inflammation and oxidative stress induced. Oral supplementation of CoQ
10
during exercise was efficient reducing oxidative stress (decreased membrane hydroperoxides, 8-OHdG and isoprostanes generation, increased catalase, and total antioxidant status), which would lead to the maintenance of the cell integrity. Data obtained also indicate that CoQ
10
prevents over-expression of TNF-α after exercise, together with an increase in sTNF-RII that limits the pro-inflammatory actions of TNF. Moreover, CoQ
10
supplementation reduced creatinine production.
Conclusions
CoQ
10
supplementation before strenuous exercise decreases the oxidative stress and modulates the inflammatory signaling, reducing the subsequent muscle damage. |
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ISSN: | 1436-6207 1436-6215 |
DOI: | 10.1007/s00394-011-0257-5 |