Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/99158
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dc.contributor.authorSlattery, K.-
dc.contributor.authorDascombe, B.-
dc.contributor.authorWallace, L.-
dc.contributor.authorBentley, D.-
dc.contributor.authorCoutts, A.-
dc.date.issued2014-
dc.identifier.citationMedicine and Science in Sports and Exercise, 2014; 46(6):1114-1123-
dc.identifier.issn0195-9131-
dc.identifier.issn1530-0315-
dc.identifier.urihttp://hdl.handle.net/2440/99158-
dc.description.abstractPurpose: This investigation examined the ergogenic effect of short-term oral N-acetylcysteine (NAC) supplementation and the associated changes in redox balance and inflammation during intense training. Methods: A double-blind randomized placebo-controlled crossover design was used to assess 9 d of oral NAC supplementation (1200 mgIdj1) in 10 well-trained triathletes. For each supplement trial (NAC and placebo), baseline venous blood and urine samples were taken, and a presupplementation cycle ergometer race simulation was performed. After the loading period, further samples were collected preexercise, postexercise, and 2 and 24 h after the postsupplementation cycle ergometer race simulation. Changes in total antioxidant capacity, ferric reducing ability of plasma, reduced glutathione, oxidized glutathione, thiobarbituric acid-reactive substances, interleukin 6, xanthine oxidase, hypoxanthine, monocyte chemotactic protein 1, nuclear factor JB, and urinary 15-isoprostane F2t concentration were assessed. The experimental procedure was repeated with the remaining supplement after a 3-wk washout. Eight participants completed both supplementation trials. Results: NAC improved sprint performance during the cycle ergometer race simulation (P G 0.001, Gp 2 = 0.03). Supplementation with NAC also augmented postexercise plasma total antioxidant capacity (P = 0.005, Gp 2 = 0.19), reduced exercise-induced oxidative damage (plasma thiobarbituric acid-reactive substances, P = 0.002, Gp 2 = 0.22; urinary 15-isoprostane F2t concentration, P = 0.010, Gp 2 = 0.431), attenuated inflammation (plasma interleukin 6, P = 0.002, Gp 2 = 0.22; monocyte chemotactic protein 1, P = 0.012, Gp 2 = 0.17), and increased postexercise nuclear factor JB activity (P G 0.001, Gp 2 = 0.21). Conclusion: Oral NAC supplementation improved cycling performance via an improved redox balance and promoted adaptive processes in well-trained athletes undergoing strenuous physical training.-
dc.description.statementofresponsibilityKatie May Slattery, Ben Dascombe, Lee Kenneth Wallace, David J. Bentley, and Aaron James Coutts-
dc.language.isoen-
dc.publisherAmerican College of Sports Medicine (ACSM)-
dc.rightsCopyright © 2014 by the American College of Sports Medicine-
dc.source.urihttp://dx.doi.org/10.1249/mss.0000000000000222-
dc.subjectAntioxidant; Oxidative stress; Inflammation; Nuclear factor κB-
dc.titleEffect of N-acetylcysteine on cycling performance after intensified training-
dc.typeJournal article-
dc.identifier.doi10.1249/MSS.0000000000000222-
pubs.publication-statusPublished-
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