Literature DB >> 30184287

Physiological adaptations to resistance training in rats selectively bred for low and high response to aerobic exercise training.

Juha P Ahtiainen1, Sanna Lensu1, Ilona Ruotsalainen2, Moritz Schumann3, Johanna K Ihalainen1, Vasco Fachada1, Christopher L Mendias4, Matthew S Brook5, Kenneth Smith5, Philip J Atherton5, Lauren G Koch6, Steven L Britton7,8, Heikki Kainulainen1.   

Abstract

NEW
FINDINGS: What is the central question of this study? Can phenotypic traits associated with low response to one mode of training be extrapolated to other exercise-inducible phenotypes? The present study investigated whether rats that are low responders to endurance training are also low responders to resistance training. What is the main finding and its importance? After resistance training, rats that are high responders to aerobic exercise training improved more in maximal strength compared with low-responder rats. However, the greater gain in strength in high-responder rats was not accompanied by muscle hypertrophy, suggesting that the responses observed could be mainly neural in origin. ABSTRACT: The purpose of this study was to determine whether rats selectively bred for low and high response to aerobic exercise training co-segregate for differences in muscle adaptations to ladder-climbing resistance training. Five high-responder (HRT) and five low-responder (LRT) rats completed the resistance training, while six HRT and six LRT rats served as sedentary control animals. Before and after the 6 week intervention, body composition was determined by dual energy X-ray absorptiometry. Before tissue harvesting, the right triceps surae muscles were loaded by electrical stimulation. Muscle fibre cross-sectional areas, nuclei per cell, phosphorylation status of selected signalling proteins of mTOR and Smad pathways, and muscle protein, DNA and RNA concentrations were determined for the right gastrocnemius muscle. The daily protein synthesis rate was determined by the deuterium oxide method from the left quadriceps femoris muscle. Tissue weights of fore- and hindlimb muscles were measured. In response to resistance training, maximal carrying capacity was greater in HRT (∼3.3 times body mass) than LRT (∼2.5 times body mass), indicating greater improvements of strength in HRT. However, muscle hypertrophy that could be related to greater strength gains in HRT was not observed. Furthermore, noteworthy changes within the experimental groups or differences between groups were not observed in the present measures. The lack of hypertrophic muscular adaptations despite considerable increases in muscular strength suggest that adaptations to the present ladder-climbing training in HRT and LRT rats were largely induced by neural adaptations.
© 2018 The Authors. Experimental Physiology © 2018 The Physiological Society.

Entities:  

Keywords:  fibre contractility; muscle hypertrophy; muscle stimulation; protein synthesis

Mesh:

Year:  2018        PMID: 30184287      PMCID: PMC6519084          DOI: 10.1113/EP087144

Source DB:  PubMed          Journal:  Exp Physiol        ISSN: 0958-0670            Impact factor:   2.969


  43 in total

Review 1.  Individual differences in response to regular physical activity.

Authors:  C Bouchard; T Rankinen
Journal:  Med Sci Sports Exerc       Date:  2001-06       Impact factor: 5.411

2.  Effects of resistance training on neuromuscular junction morphology.

Authors:  M R Deschenes; D A Judelson; W J Kraemer; V J Meskaitis; J S Volek; B C Nindl; F S Harman; D R Deaver
Journal:  Muscle Nerve       Date:  2000-10       Impact factor: 3.217

3.  High responders to resistance exercise training demonstrate differential regulation of skeletal muscle microRNA expression.

Authors:  Peter K Davidsen; Iain J Gallagher; Joseph W Hartman; Mark A Tarnopolsky; Flemming Dela; Jørn W Helge; James A Timmons; Stuart M Phillips
Journal:  J Appl Physiol (1985)       Date:  2010-10-28

4.  Potent myofiber hypertrophy during resistance training in humans is associated with satellite cell-mediated myonuclear addition: a cluster analysis.

Authors:  John K Petrella; Jeong-Su Kim; David L Mayhew; James M Cross; Marcas M Bamman
Journal:  J Appl Physiol (1985)       Date:  2008-04-24

5.  Variability in muscle size and strength gain after unilateral resistance training.

Authors:  Monica J Hubal; Heather Gordish-Dressman; Paul D Thompson; Thomas B Price; Eric P Hoffman; Theodore J Angelopoulos; Paul M Gordon; Niall M Moyna; Linda S Pescatello; Paul S Visich; Robert F Zoeller; Richard L Seip; Priscilla M Clarkson
Journal:  Med Sci Sports Exerc       Date:  2005-06       Impact factor: 5.411

Review 6.  Animal models for inducing muscle hypertrophy: are they relevant for clinical applications in humans?

Authors:  Dawn A Lowe; Stephen E Alway
Journal:  J Orthop Sports Phys Ther       Date:  2002-02       Impact factor: 4.751

7.  Physiological hypertrophy of the FHL muscle following 8 weeks of progressive resistance exercise in the rat.

Authors:  Troy A Hornberger; Roger P Farrar
Journal:  Can J Appl Physiol       Date:  2004-02

8.  Viral expression of insulin-like growth factor-I enhances muscle hypertrophy in resistance-trained rats.

Authors:  Sukho Lee; Elisabeth R Barton; H Lee Sweeney; Roger P Farrar
Journal:  J Appl Physiol (1985)       Date:  2004-03

9.  Cluster analysis tests the importance of myogenic gene expression during myofiber hypertrophy in humans.

Authors:  Marcas M Bamman; John K Petrella; Jeong-su Kim; David L Mayhew; James M Cross
Journal:  J Appl Physiol (1985)       Date:  2007-03-29

10.  Resistance training improves femoral artery endothelial dysfunction in aged rats.

Authors:  M Brennan Harris; Kristen N Slack; David T Prestosa; David J Hryvniak
Journal:  Eur J Appl Physiol       Date:  2009-10-27       Impact factor: 3.078

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  3 in total

1.  Low responders to endurance training exhibit impaired hypertrophy and divergent biological process responses in rat skeletal muscle.

Authors:  Daniel W D West; Thomas M Doering; Jamie-Lee M Thompson; Boris P Budiono; Sarah J Lessard; Lauren G Koch; Steven L Britton; Roland Steck; Nuala M Byrne; Matthew A Brown; Jonathan M Peake; Kevin J Ashton; Vernon G Coffey
Journal:  Exp Physiol       Date:  2021-02-05       Impact factor: 2.969

2.  Branched-Chain Amino Acid Deprivation Decreases Lipid Oxidation and Lipogenesis in C2C12 Myotubes.

Authors:  Sira Karvinen; Vasco Fachada; Ulla-Maria Sahinaho; Satu Pekkala; Juulia H Lautaoja; Sakari Mäntyselkä; Perttu Permi; Juha J Hulmi; Mika Silvennoinen; Heikki Kainulainen
Journal:  Metabolites       Date:  2022-04-05

3.  Comparative Analysis of Skeletal Muscle Transcriptional Signatures Associated With Aerobic Exercise Capacity or Response to Training in Humans and Rats.

Authors:  Yildiz Kelahmetoglu; Paulo R Jannig; Igor Cervenka; Lauren G Koch; Steven L Britton; Jiajia Zhou; Huating Wang; Matthew M Robinson; K Sreekumaran Nair; Jorge L Ruas
Journal:  Front Endocrinol (Lausanne)       Date:  2020-10-26       Impact factor: 5.555

  3 in total

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