Aerobic Exercise Alters Skeletal Muscle Molecular Responses to Resistance Exercise
Abstract
PURPOSE: This study assessed the influence of an acute aerobic exercise bout on molecular responses to subsequent resistance exercise (RE). METHODS: Nine physically active men performed a 45-min one-legged cycle ergometry exercise and 4 × 7 maximal concentric-eccentric knee extensions for each leg 6 h later. Thus, one limb was subjected to aerobic and resistance exercise (AE+RE), and the contralateral limb to resistance exercise (RE) only. Knee extensor peak power was determined. Biopsies were obtained from the m vastus lateralis before (PRE) and 15 min (POST1) and 3 h after RE. Analysis determined glycogen content, mRNA levels (vascular endothelial growth factor, peroxisome proliferator-activated receptor-γ coactivator-1, muscle RING-finger protein-1, atrogin-1, myostatin), and phosphorylated proteins (mammalian target of rapamycin, p70S6 kinase, ribosomal protein S6, eukaryotic elongation factor 2). RESULTS: Peak power was similar in AE + RE and RE. After RE, the time course of glycogen utilization and protein signaling was similar across legs. However, phosphorylation of mammalian target of rapamycin and p70S6 kinase was elevated in AE + RE versus RE (main effect, P < 0.05). Vascular endothelial growth factor and peroxisome proliferator-activated receptor-γ coactivator-1 were higher in AE + RE than in RE at PRE and POST1 (P < 0.05). Myostatin was lower in AE + RE versus RE at PRE and POST1 (P < 0.05) and downregulated after resistance exercise only. Atrogin-1 was higher in AE + RE than in RE at PRE and POST1 (P < 0.05) and decreased after RE in AE + RE. Muscle RING-finger protein-1 was similar across legs. No difference for any marker was evident 3 h after RE. CONCLUSIONS: These results suggest that acute aerobic exercise alters molecular events regulating muscle protein turnover during the early recovery period from subsequent RE.
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A low-intensity endurance session will not affect signaling pathways regulating strength gains.
“the low-intensity session will not affect signaling pathways regulating strength gains [51–53].”
From Using Molecular Biology to Maximize Concurrent Training (2014) · cites this paper as [52]
Lundberg et al. [52] found no inhibition of mTOR activation when subjects performed 45 min of cycling at 70% VO2max 6 h before resistance exercise.
“Lundberg et al. did not find any inhibition of mTOR activation when subjects performed 45 min of cycling at 70 % VO2max 6 h before performing resistance exercise [52].”
From Using Molecular Biology to Maximize Concurrent Training (2014) · cites this paper as [52]
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- Authors
- LUNDBERG, T. R., FERNANDEZ-GONZALO, R., GUSTAFSSON, T., & TESCH, P. A.
- Affiliations
- Mid Sweden University (SE)
- Karolinska University Hospital (SE)
- Karolinska Institutet (SE)
- Venue
- Medicine & Science in Sports & Exercise
- Published
- 2012-09
- Volume
- 44
- Issue
- 9
- Pages
- 1680-1688
- ISSN
- 0195-9131 (ISSN-L)
- OpenAlex
- W2029557372
- Cited by
- 86
- References
- 40
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 3 · 2023: 6 · 2022: 6 · 2021: 3 · 2020: 4 · 2019: 4 · 2018: 7 · 2017: 6 · 2016: 6 · 2015: 14 · 2014: 15 · 2013: 7 · 2012: 1
- FWCI
- 5.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Medicine & Science in Sports & Exercise (publishedVersion, public-domain)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Complementary and alternative medicine › Cardiovascular and exercise physiology
- Keywords
- aerobic exercise, resistance training, skeletal muscle, muscle protein turnover, mTOR signaling, p70 S6 kinase, ribosomal protein S6, elongation factor 2, myostatin, atrogin-1, vascular endothelial growth factor, PPAR-gamma coactivator 1, muscle glycogen, vastus lateralis, knee extension, post-exercise recovery
- MeSH terms
- Adult, Glycogen, Humans, Male, Muscle Proteins, Phosphorylation, RNA, Messenger, Blotting, Western, Exercise, Ergometry, Muscle, Skeletal, Resistance Training, Young Adult, Real-Time Polymerase Chain Reaction
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