Impact of resistance exercise on ribosome biogenesis is acutely regulated by post‐exercise recovery strategies

Muscle hypertrophy occurs following increased protein synthesis, which requires activation of the ribosomal complex. Additionally, increased translational capacity via elevated ribosomal RNA (rRNA) synthesis has also been implicated in resistance training‐induced skeletal muscle hypertrophy. The tim...

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Veröffentlicht in:Physiological reports 2016-01, Vol.4 (2), p.e12670-n/a
Hauptverfasser: Figueiredo, Vandré C., Roberts, Llion A., Markworth, James F., Barnett, Matthew P. G., Coombes, Jeff S., Raastad, Truls, Peake, Jonathan M., Cameron‐Smith, David
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container_issue 2
container_start_page e12670
container_title Physiological reports
container_volume 4
creator Figueiredo, Vandré C.
Roberts, Llion A.
Markworth, James F.
Barnett, Matthew P. G.
Coombes, Jeff S.
Raastad, Truls
Peake, Jonathan M.
Cameron‐Smith, David
description Muscle hypertrophy occurs following increased protein synthesis, which requires activation of the ribosomal complex. Additionally, increased translational capacity via elevated ribosomal RNA (rRNA) synthesis has also been implicated in resistance training‐induced skeletal muscle hypertrophy. The time course of ribosome biogenesis following resistance exercise (RE) and the impact exerted by differing recovery strategies remains unknown. In the present study, the activation of transcriptional regulators, the expression levels of pre‐rRNA, and mature rRNA components were measured through 48 h after a single‐bout RE. In addition, the effects of either low‐intensity cycling (active recovery, ACT) or a cold‐water immersion (CWI) recovery strategy were compared. Nine male subjects performed two bouts of high‐load RE randomized to be followed by 10 min of either ACT or CWI. Muscle biopsies were collected before RE and at 2, 24, and 48 h after RE. RE increased the phosphorylation of the p38‐MNK1‐eIF4E axis, an effect only evident with ACT recovery. Downstream, cyclin D1 protein, total eIF4E, upstream binding factor 1 (UBF1), and c‐Myc proteins were all increased only after RE with ACT. This corresponded with elevated abundance of the pre‐rRNAs (45S, ITS‐28S, ITS‐5.8S, and ETS‐18S) from 24 h after RE with ACT. In conclusion, coordinated upstream signaling and activation of transcriptional factors stimulated pre‐rRNA expression after RE. CWI, as a recovery strategy, markedly blunted these events, suggesting that suppressed ribosome biogenesis may be one factor contributing to the impaired hypertrophic response observed when CWI is used regularly after exercise. Signalling pathway leading to rDNA transcription affected by resistance exercise and recovery strategies.
doi_str_mv 10.14814/phy2.12670
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G. ; Coombes, Jeff S. ; Raastad, Truls ; Peake, Jonathan M. ; Cameron‐Smith, David</creator><creatorcontrib>Figueiredo, Vandré C. ; Roberts, Llion A. ; Markworth, James F. ; Barnett, Matthew P. G. ; Coombes, Jeff S. ; Raastad, Truls ; Peake, Jonathan M. ; Cameron‐Smith, David</creatorcontrib><description>Muscle hypertrophy occurs following increased protein synthesis, which requires activation of the ribosomal complex. Additionally, increased translational capacity via elevated ribosomal RNA (rRNA) synthesis has also been implicated in resistance training‐induced skeletal muscle hypertrophy. The time course of ribosome biogenesis following resistance exercise (RE) and the impact exerted by differing recovery strategies remains unknown. In the present study, the activation of transcriptional regulators, the expression levels of pre‐rRNA, and mature rRNA components were measured through 48 h after a single‐bout RE. In addition, the effects of either low‐intensity cycling (active recovery, ACT) or a cold‐water immersion (CWI) recovery strategy were compared. Nine male subjects performed two bouts of high‐load RE randomized to be followed by 10 min of either ACT or CWI. Muscle biopsies were collected before RE and at 2, 24, and 48 h after RE. RE increased the phosphorylation of the p38‐MNK1‐eIF4E axis, an effect only evident with ACT recovery. Downstream, cyclin D1 protein, total eIF4E, upstream binding factor 1 (UBF1), and c‐Myc proteins were all increased only after RE with ACT. This corresponded with elevated abundance of the pre‐rRNAs (45S, ITS‐28S, ITS‐5.8S, and ETS‐18S) from 24 h after RE with ACT. In conclusion, coordinated upstream signaling and activation of transcriptional factors stimulated pre‐rRNA expression after RE. CWI, as a recovery strategy, markedly blunted these events, suggesting that suppressed ribosome biogenesis may be one factor contributing to the impaired hypertrophic response observed when CWI is used regularly after exercise. Signalling pathway leading to rDNA transcription affected by resistance exercise and recovery strategies.</description><identifier>ISSN: 2051-817X</identifier><identifier>EISSN: 2051-817X</identifier><identifier>DOI: 10.14814/phy2.12670</identifier><identifier>PMID: 26818586</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Biosynthesis ; Blotting, Western ; Cell cycle ; Cold ; Cold Temperature ; Cross-Over Studies ; Cyclin D1 ; D1 protein ; Endurance and Performance ; Gene expression ; Humans ; Hypertrophy ; Immunoglobulins ; Initiation factor eIF-4E ; Kinases ; Laboratories ; Male ; Muscle Metabolism ; Muscle, Skeletal - metabolism ; Musculoskeletal system ; Myc protein ; Original Research ; Phosphorylation ; Physical training ; Physiology ; pre‐rRNA ; Protein biosynthesis ; Protein synthesis ; Proteins ; Resistance Training - methods ; Reverse Transcriptase Polymerase Chain Reaction ; Ribosomal DNA ; ribosomal RNA ; Ribosomes - metabolism ; RNA polymerase ; rRNA ; Signalling Pathways ; Skeletal Muscle ; Sports training ; Strength training ; Studies ; Transcription activation ; Transcription factors ; upstream binding factor ; Young Adult</subject><ispartof>Physiological reports, 2016-01, Vol.4 (2), p.e12670-n/a</ispartof><rights>2016 The Authors. published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.</rights><rights>2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.</rights><rights>2016. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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In the present study, the activation of transcriptional regulators, the expression levels of pre‐rRNA, and mature rRNA components were measured through 48 h after a single‐bout RE. In addition, the effects of either low‐intensity cycling (active recovery, ACT) or a cold‐water immersion (CWI) recovery strategy were compared. Nine male subjects performed two bouts of high‐load RE randomized to be followed by 10 min of either ACT or CWI. Muscle biopsies were collected before RE and at 2, 24, and 48 h after RE. RE increased the phosphorylation of the p38‐MNK1‐eIF4E axis, an effect only evident with ACT recovery. Downstream, cyclin D1 protein, total eIF4E, upstream binding factor 1 (UBF1), and c‐Myc proteins were all increased only after RE with ACT. This corresponded with elevated abundance of the pre‐rRNAs (45S, ITS‐28S, ITS‐5.8S, and ETS‐18S) from 24 h after RE with ACT. In conclusion, coordinated upstream signaling and activation of transcriptional factors stimulated pre‐rRNA expression after RE. CWI, as a recovery strategy, markedly blunted these events, suggesting that suppressed ribosome biogenesis may be one factor contributing to the impaired hypertrophic response observed when CWI is used regularly after exercise. 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G.</au><au>Coombes, Jeff S.</au><au>Raastad, Truls</au><au>Peake, Jonathan M.</au><au>Cameron‐Smith, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of resistance exercise on ribosome biogenesis is acutely regulated by post‐exercise recovery strategies</atitle><jtitle>Physiological reports</jtitle><addtitle>Physiol Rep</addtitle><date>2016-01</date><risdate>2016</risdate><volume>4</volume><issue>2</issue><spage>e12670</spage><epage>n/a</epage><pages>e12670-n/a</pages><issn>2051-817X</issn><eissn>2051-817X</eissn><abstract>Muscle hypertrophy occurs following increased protein synthesis, which requires activation of the ribosomal complex. Additionally, increased translational capacity via elevated ribosomal RNA (rRNA) synthesis has also been implicated in resistance training‐induced skeletal muscle hypertrophy. The time course of ribosome biogenesis following resistance exercise (RE) and the impact exerted by differing recovery strategies remains unknown. In the present study, the activation of transcriptional regulators, the expression levels of pre‐rRNA, and mature rRNA components were measured through 48 h after a single‐bout RE. In addition, the effects of either low‐intensity cycling (active recovery, ACT) or a cold‐water immersion (CWI) recovery strategy were compared. Nine male subjects performed two bouts of high‐load RE randomized to be followed by 10 min of either ACT or CWI. Muscle biopsies were collected before RE and at 2, 24, and 48 h after RE. RE increased the phosphorylation of the p38‐MNK1‐eIF4E axis, an effect only evident with ACT recovery. Downstream, cyclin D1 protein, total eIF4E, upstream binding factor 1 (UBF1), and c‐Myc proteins were all increased only after RE with ACT. This corresponded with elevated abundance of the pre‐rRNAs (45S, ITS‐28S, ITS‐5.8S, and ETS‐18S) from 24 h after RE with ACT. In conclusion, coordinated upstream signaling and activation of transcriptional factors stimulated pre‐rRNA expression after RE. CWI, as a recovery strategy, markedly blunted these events, suggesting that suppressed ribosome biogenesis may be one factor contributing to the impaired hypertrophic response observed when CWI is used regularly after exercise. Signalling pathway leading to rDNA transcription affected by resistance exercise and recovery strategies.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>26818586</pmid><doi>10.14814/phy2.12670</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Biosynthesis
Blotting, Western
Cell cycle
Cold
Cold Temperature
Cross-Over Studies
Cyclin D1
D1 protein
Endurance and Performance
Gene expression
Humans
Hypertrophy
Immunoglobulins
Initiation factor eIF-4E
Kinases
Laboratories
Male
Muscle Metabolism
Muscle, Skeletal - metabolism
Musculoskeletal system
Myc protein
Original Research
Phosphorylation
Physical training
Physiology
pre‐rRNA
Protein biosynthesis
Protein synthesis
Proteins
Resistance Training - methods
Reverse Transcriptase Polymerase Chain Reaction
Ribosomal DNA
ribosomal RNA
Ribosomes - metabolism
RNA polymerase
rRNA
Signalling Pathways
Skeletal Muscle
Sports training
Strength training
Studies
Transcription activation
Transcription factors
upstream binding factor
Young Adult
title Impact of resistance exercise on ribosome biogenesis is acutely regulated by post‐exercise recovery strategies
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