Literature DB >> 8423838

Distinguishing unloading- versus reloading-induced changes in rat soleus muscle.

B B Krippendorf1, D A Riley.   

Abstract

Previously, solei from rats orbited 12.5 days aboard Cosmos 1887 biosatellite were biopsied 48-56 hours postflight. These atrophic muscles showed severe pathology. Designing a ground-based model of that space flight, we tested the hypothesis that 48 hours of postflight muscle reloading induced pathological changes. Rats were subjected to 12.5 days of hindlimb suspension unloading and biopsied immediately after suspension or after returning to normal weightbearing 12, 24, or 48 hours. Soleus morphological changes were quantitated on histochemically and immunohistochemically stained cross-sections. Solei from 0-hour reloaded rats showed significantly decreased wet weights, diminished myofiber cross-sectional area, angular myofibers, myofibril disruption, and more myofibers expressing fast myosin. Compared with suspension alone (0-hour reloading), reloading 12-48 hours induced slightly increased soleus wet weights, myofiber swelling, significant interstitial tissue edema, macrophage activation, and monocyte infiltration. These results suggest the degree and type of muscle degenerative changes observed postflight depend on the duration of gravity readaptation before biopsy and not solely on exposure to microgravity.

Entities:  

Keywords:  NASA Discipline Musculoskeletal; NASA Discipline Number 00-00; NASA Experiment Number COS 1887-6; NASA Program Flight; Non-NASA Center

Mesh:

Substances:

Year:  1993        PMID: 8423838     DOI: 10.1002/mus.880160116

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  27 in total

1.  Cytoplasm-to-myonucleus ratios following microgravity.

Authors:  C E Kasper; L Xun
Journal:  J Muscle Res Cell Motil       Date:  1996-10       Impact factor: 2.698

2.  Agent-based computational model investigates muscle-specific responses to disuse-induced atrophy.

Authors:  Kyle S Martin; Silvia S Blemker; Shayn M Peirce
Journal:  J Appl Physiol (1985)       Date:  2015-02-26

3.  IL-10 triggers changes in macrophage phenotype that promote muscle growth and regeneration.

Authors:  Bo Deng; Michelle Wehling-Henricks; S Armando Villalta; Ying Wang; James G Tidball
Journal:  J Immunol       Date:  2012-08-29       Impact factor: 5.422

4.  Regrowth after skeletal muscle atrophy is impaired in aged rats, despite similar responses in signaling pathways.

Authors:  Jena R White; Amy L Confides; Stephanie Moore-Reed; Johanna M Hoch; Esther E Dupont-Versteegden
Journal:  Exp Gerontol       Date:  2015-02-12       Impact factor: 4.032

Review 5.  Regulatory interactions between muscle and the immune system during muscle regeneration.

Authors:  James G Tidball; S Armando Villalta
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2010-03-10       Impact factor: 3.619

6.  Null mutation of myeloperoxidase in mice prevents mechanical activation of neutrophil lysis of muscle cell membranes in vitro and in vivo.

Authors:  Hal X Nguyen; Aldons J Lusis; James G Tidball
Journal:  J Physiol       Date:  2005-03-24       Impact factor: 5.182

7.  Changes in muscle T2 relaxation properties following spinal cord injury and locomotor training.

Authors:  Min Liu; Prodip Bose; Glenn A Walter; Douglas K Anderson; Floyd J Thompson; Krista Vandenborne
Journal:  Eur J Appl Physiol       Date:  2006-04-25       Impact factor: 3.078

8.  Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy.

Authors:  S Armando Villalta; Hal X Nguyen; Bo Deng; Tomomi Gotoh; James G Tidball
Journal:  Hum Mol Genet       Date:  2008-11-07       Impact factor: 6.150

9.  Coordinate activation of lysosomal, Ca 2+-activated and ATP-ubiquitin-dependent proteinases in the unweighted rat soleus muscle.

Authors:  D Taillandier; E Aurousseau; D Meynial-Denis; D Bechet; M Ferrara; P Cottin; A Ducastaing; X Bigard; C Y Guezennec; H P Schmid
Journal:  Biochem J       Date:  1996-05-15       Impact factor: 3.857

10.  Null mutation of gp91phox reduces muscle membrane lysis during muscle inflammation in mice.

Authors:  Hal X Nguyen; James G Tidball
Journal:  J Physiol       Date:  2003-10-10       Impact factor: 5.182

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