9 results on '"concurrent exercise"'
Search Results
2. Resistance exercise-induced S6K1 kinase activity is not inhibited in human skeletal muscle despite prior activation of AMPK by high-intensity interval cycling
- Author
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Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
Combining endurance and strength training in the same session has been reported to reduce the anabolic response to the latter form of exercise. The underlying mechanism, based primarily on results from rodent muscle, is proposed to involve AMPK-dependent inhibition of mTORC1 signaling. This hypothesis was tested in eight trained male subjects who in randomized order performed either resistance exercise only (R) or interval cycling followed by resistance exercise (ER). Biopsies taken from the vastus lateralis before and after endurance exercise and repeatedly after resistance exercise were assessed for glycogen content, kinase activity, protein phosphorylation, and gene expression. Mixed muscle fractional synthetic rate was measured at rest and during 3 h of recovery using the stable isotope technique. In ER, AMPK activity was elevated immediately after both endurance and resistance exercise (similar to 90%, P < 0.05) but was unchanged in R. Thr(389) phosphorylation of S6K1 was increased severalfold immediately after exercise (P < 0.05) in both trials and increased further throughout recovery. After 90 and 180 min recovery, S6K1 activity was elevated (similar to 55 and similar to 110%, respectively, P < 0.05) and eukaryotic elongation factor 2 phosphorylation was reduced (similar to 55%, P < 0.05) with no difference between trials. In contrast, markers for protein catabolism were differently influenced by the two modes of exercise; ER induced a significant increase in gene and protein expression of MuRF1 (P < 0.05), which was not observed following R exercise only. In conclusion, cycling-induced elevation in AMPK activity does not inhibit mTOR complex 1 signaling after subsequent resistance exercise but may instead interfere with the hypertrophic response by influencing key components in protein breakdown.
- Published
- 2015
- Full Text
- View/download PDF
3. Resistance exercise-induced S6K1 kinase activity is not inhibited in human skeletal muscle despite prior activation of AMPK by high-intensity interval cycling
- Author
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Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
Combining endurance and strength training in the same session has been reported to reduce the anabolic response to the latter form of exercise. The underlying mechanism, based primarily on results from rodent muscle, is proposed to involve AMPK-dependent inhibition of mTORC1 signaling. This hypothesis was tested in eight trained male subjects who in randomized order performed either resistance exercise only (R) or interval cycling followed by resistance exercise (ER). Biopsies taken from the vastus lateralis before and after endurance exercise and repeatedly after resistance exercise were assessed for glycogen content, kinase activity, protein phosphorylation, and gene expression. Mixed muscle fractional synthetic rate was measured at rest and during 3 h of recovery using the stable isotope technique. In ER, AMPK activity was elevated immediately after both endurance and resistance exercise (similar to 90%, P < 0.05) but was unchanged in R. Thr(389) phosphorylation of S6K1 was increased severalfold immediately after exercise (P < 0.05) in both trials and increased further throughout recovery. After 90 and 180 min recovery, S6K1 activity was elevated (similar to 55 and similar to 110%, respectively, P < 0.05) and eukaryotic elongation factor 2 phosphorylation was reduced (similar to 55%, P < 0.05) with no difference between trials. In contrast, markers for protein catabolism were differently influenced by the two modes of exercise; ER induced a significant increase in gene and protein expression of MuRF1 (P < 0.05), which was not observed following R exercise only. In conclusion, cycling-induced elevation in AMPK activity does not inhibit mTOR complex 1 signaling after subsequent resistance exercise but may instead interfere with the hypertrophic response by influencing key components in protein breakdown.
- Published
- 2015
- Full Text
- View/download PDF
4. Resistance exercise-induced S6K1 kinase activity is not inhibited in human skeletal muscle despite prior activation of AMPK by high-intensity interval cycling
- Author
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Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
Combining endurance and strength training in the same session has been reported to reduce the anabolic response to the latter form of exercise. The underlying mechanism, based primarily on results from rodent muscle, is proposed to involve AMPK-dependent inhibition of mTORC1 signaling. This hypothesis was tested in eight trained male subjects who in randomized order performed either resistance exercise only (R) or interval cycling followed by resistance exercise (ER). Biopsies taken from the vastus lateralis before and after endurance exercise and repeatedly after resistance exercise were assessed for glycogen content, kinase activity, protein phosphorylation, and gene expression. Mixed muscle fractional synthetic rate was measured at rest and during 3 h of recovery using the stable isotope technique. In ER, AMPK activity was elevated immediately after both endurance and resistance exercise (similar to 90%, P < 0.05) but was unchanged in R. Thr(389) phosphorylation of S6K1 was increased severalfold immediately after exercise (P < 0.05) in both trials and increased further throughout recovery. After 90 and 180 min recovery, S6K1 activity was elevated (similar to 55 and similar to 110%, respectively, P < 0.05) and eukaryotic elongation factor 2 phosphorylation was reduced (similar to 55%, P < 0.05) with no difference between trials. In contrast, markers for protein catabolism were differently influenced by the two modes of exercise; ER induced a significant increase in gene and protein expression of MuRF1 (P < 0.05), which was not observed following R exercise only. In conclusion, cycling-induced elevation in AMPK activity does not inhibit mTOR complex 1 signaling after subsequent resistance exercise but may instead interfere with the hypertrophic response by influencing key components in protein breakdown.
- Published
- 2015
- Full Text
- View/download PDF
5. Resistance exercise-induced S6K1 kinase activity is not inhibited in human skeletal muscle despite prior activation of AMPK by high-intensity interval cycling
- Author
-
Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
Combining endurance and strength training in the same session has been reported to reduce the anabolic response to the latter form of exercise. The underlying mechanism, based primarily on results from rodent muscle, is proposed to involve AMPK-dependent inhibition of mTORC1 signaling. This hypothesis was tested in eight trained male subjects who in randomized order performed either resistance exercise only (R) or interval cycling followed by resistance exercise (ER). Biopsies taken from the vastus lateralis before and after endurance exercise and repeatedly after resistance exercise were assessed for glycogen content, kinase activity, protein phosphorylation, and gene expression. Mixed muscle fractional synthetic rate was measured at rest and during 3 h of recovery using the stable isotope technique. In ER, AMPK activity was elevated immediately after both endurance and resistance exercise (similar to 90%, P < 0.05) but was unchanged in R. Thr(389) phosphorylation of S6K1 was increased severalfold immediately after exercise (P < 0.05) in both trials and increased further throughout recovery. After 90 and 180 min recovery, S6K1 activity was elevated (similar to 55 and similar to 110%, respectively, P < 0.05) and eukaryotic elongation factor 2 phosphorylation was reduced (similar to 55%, P < 0.05) with no difference between trials. In contrast, markers for protein catabolism were differently influenced by the two modes of exercise; ER induced a significant increase in gene and protein expression of MuRF1 (P < 0.05), which was not observed following R exercise only. In conclusion, cycling-induced elevation in AMPK activity does not inhibit mTOR complex 1 signaling after subsequent resistance exercise but may instead interfere with the hypertrophic response by influencing key components in protein breakdown.
- Published
- 2015
- Full Text
- View/download PDF
6. Resistance exercise-induced S6K1 kinase activity is not inhibited in human skeletal muscle despite prior activation of AMPK by high-intensity interval cycling
- Author
-
Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Apro, William, Moberg, Marcus, Hamilton, D. Lee, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
Combining endurance and strength training in the same session has been reported to reduce the anabolic response to the latter form of exercise. The underlying mechanism, based primarily on results from rodent muscle, is proposed to involve AMPK-dependent inhibition of mTORC1 signaling. This hypothesis was tested in eight trained male subjects who in randomized order performed either resistance exercise only (R) or interval cycling followed by resistance exercise (ER). Biopsies taken from the vastus lateralis before and after endurance exercise and repeatedly after resistance exercise were assessed for glycogen content, kinase activity, protein phosphorylation, and gene expression. Mixed muscle fractional synthetic rate was measured at rest and during 3 h of recovery using the stable isotope technique. In ER, AMPK activity was elevated immediately after both endurance and resistance exercise (similar to 90%, P < 0.05) but was unchanged in R. Thr(389) phosphorylation of S6K1 was increased severalfold immediately after exercise (P < 0.05) in both trials and increased further throughout recovery. After 90 and 180 min recovery, S6K1 activity was elevated (similar to 55 and similar to 110%, respectively, P < 0.05) and eukaryotic elongation factor 2 phosphorylation was reduced (similar to 55%, P < 0.05) with no difference between trials. In contrast, markers for protein catabolism were differently influenced by the two modes of exercise; ER induced a significant increase in gene and protein expression of MuRF1 (P < 0.05), which was not observed following R exercise only. In conclusion, cycling-induced elevation in AMPK activity does not inhibit mTOR complex 1 signaling after subsequent resistance exercise but may instead interfere with the hypertrophic response by influencing key components in protein breakdown.
- Published
- 2015
- Full Text
- View/download PDF
7. Truncated splice variant PGC-1 alpha 4 is not associated with exercise-induced human muscle hypertrophy
- Author
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Lundberg, Tommy, Fernandez-Gonzalo, Rodrigo, Norrbom, Jessica, Fischer, Helene, Tesch, Per, Gustafsson, Thomas, Lundberg, Tommy, Fernandez-Gonzalo, Rodrigo, Norrbom, Jessica, Fischer, Helene, Tesch, Per, and Gustafsson, Thomas
- Abstract
Introduction: A truncated PGC-1 alpha splice variant (PGC-1 alpha 4) has been implicated in the regulation of resistance exercise (RE)-induced muscle hypertrophy, and basal expression levels said to be augmented in response to concurrent aerobic (AE) and RE training.Aim: The current study investigated human muscle truncated and non-truncated PGC-1a transcripts in response to both acute and chronic RE, and with or without preceding AE (AE+RE).Methods: Ten men performed 5 weeks of unilateral AE+RE and RE training.Before (untrained) and after (trained) this intervention, PGC-1a transcripts were assessed in vastus lateralis muscle biopsies obtained before and 3 h after acute RE, with or without preceding AE.Additionally, samples were collected 72 h after the last exercise bout of the training programme.Results: The truncated splice variant increased (P < 0.05) its expression after acute exercise regardless of mode. However, the expression was greater (P < 0.05) after AE+RE than RE. Other PGC-1a transcripts showed similar response. Truncated transcripts originated from both the alternative and proximal promoter, and AE+RE increasedPGC-1 alpha expression from both promoter sites. RE induced transcripts from the alternative promoter only. PGC-1 alpha expressions after acute exercise were comparable across isoforms in both untrained and trained muscle. Steady-state levels of isoforms were unchanged after 5-week training (P > 0.05). Exercise-induced expression of PGC-1a variants did not correlate with changes in muscle size or strength (P > 0.05).Conclusion: Our results do not support the view that truncated PGC-1a coordinates exercise-induced hypertrophy in human skeletal muscle.Rather, all PGC-1 alpha isoforms appear to be regulated transiently in response to acute exercise and regardless of mode.
- Published
- 2014
- Full Text
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8. Acute molecular responses in untrained and trained muscle subjected to aerobic and resistance exercise training versus resistance training alone
- Author
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Fernandez-Gonzalo, R., Lundberg, Tommy R., Tesch, Per A., Fernandez-Gonzalo, R., Lundberg, Tommy R., and Tesch, Per A.
- Abstract
AimThis study assessed and compared acute muscle molecular responses before and after 5-week training, employing either aerobic (AE) and resistance exercise (RE) or RE only. MethodsTen men performed one-legged RE, while the contralateral limb performed AE followed by RE 6h later (AE+RE). Before (untrained) and after (trained) the intervention, acute bouts of RE were performed with or without preceding AE. Biopsies were obtained from m. vastus lateralis of each leg pre- and 3h post-RE to determine mRNA levels of VEGF, PGC-1, MuRF-1, atrogin-1, myostatin and phosphorylation of mTOR, p70S6K, rpS6 and eEF2. ResultsPGC-1 and VEGF expression increased (P<0.05) after acute RE in the untrained, but not the trained state. These markers showed greater response after AE+RE than RE in either condition. Myostatin was lower after AE+RE than RE, both before and after training. AE+RE showed higher MuRF-1 and atrogin-1 expression than RE in the untrained, not the trained state. Exercise increased (P<0.05) p70S6K phosphorylation both before and after training, yet this increase tended to be more prominent for AE+RE than RE before training. Phosphorylation of p70S6K was greater in trained muscle. Changes in these markers did not correlate with exercise-induced alterations in strength or muscle size. ConclusionConcurrent exercise in untrained skeletal muscle prompts global molecular responses consistent with resulting whole muscle adaptations. Yet, training blunts the more robust anabolic response shown after AE+RE compared with RE. This study challenges the concept that single molecular markers could predict training-induced changes in muscle size or strength.
- Published
- 2013
- Full Text
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9. Lower body endurance exercise acutely affects resistance exercise induced transcriptional and translational signalling in the tricpes brachii muscle
- Author
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Marcus, Moberg, Apró, William, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, Blomstrand, Eva, Marcus, Moberg, Apró, William, Ekblom, Björn, van Hall, Gerrit, Holmberg, Hans-Christer, and Blomstrand, Eva
- Abstract
At the time of Marcus Moberg's dissertation this was a manuscript.
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