Oral quercetin supplementation hampers skeletal muscle adaptations in response to exercise training |
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Authors: | R A Casuso E J Martínez‐López N B Nordsborg F Hita‐Contreras R Martínez‐Romero A Cañuelo A Martínez‐Amat |
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Institution: | 1. Department of Health Sciences, University of Jaén, , Jaén, Spain;2. Department of Music, Plastic Expression and Body Language, University of Jaén, , Jaén, Spain;3. Department of Nutrition, Exercise and Sport, University of Copenhagen, , Copenhagen, Denmark;4. Department of Experimental Biology, University of Jaén, , Jaén, Spain |
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Abstract: | We aimed to test exercise‐induced adaptations on skeletal muscle when quercetin is supplemented. Four groups of rats were tested: quercetin sedentary, quercetin exercised, placebo sedentary, and placebo exercised. Treadmill exercise training took place 5 days a week for 6 weeks. Quercetin groups were supplemented with quercetin, via gavage, on alternate days throughout the experimental period. Sirtuin 1 (SIRT1), peroxisome proliferator‐activated receptor γ coactivator‐1α mRNA levels, mitochondrial DNA (mtDNA) content, and citrate synthase (CS) activity were measured on quadriceps muscle. Redox status was also quantified by measuring muscle antioxidant enzymatic activity and oxidative damage product, such as protein carbonyl content (PCC). Quercetin supplementation increased oxidative damage in both exercised and sedentary rats by inducing higher amounts of PCC (P < 0.001). Quercetin supplementation caused higher catalase (P < 0.001) and superoxide dismutase (P < 0.05) activity in the non‐exercised animals, but not when quercetin is supplemented during exercise. Quercetin supplementation increased SIRT1 expression, but when quercetin is supplemented during exercise, this effect is abolished (P < 0.001). The combination of exercise and quercetin supplementation caused lower (P < 0.05) mtDNA content and CS activity when compared with exercise alone. Quercetin supplementation during exercise provides a disadvantage to exercise‐induced muscle adaptations. |
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Keywords: | Flavonoids SIRT1 PGC‐1α training oxidative damage |
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