FASEB J. Mp Biomedicals
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text Free
Right arrow Full Text (PDF) Free
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by VANDENBURGH, H.
Right arrow Articles by LEMAIRE, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by VANDENBURGH, H.
Right arrow Articles by LEMAIRE, J.
(The FASEB Journal. 1999;13:1031-1038.)
© 1999 FASEB

Space travel directly induces skeletal muscle atrophy

HERMAN VANDENBURGH*,{dagger}1, JOSEPH CHROMIAK*, JANET SHANSKY*, MICHAEL DEL TATTO* and JULIE LEMAIRE*

* Department of Pathology, Brown University School of Medicine and The Miriam Hospital, Providence, Rhode Island 02906, USA; and
{dagger} Department of Molecular Pharmacology, Physiology, and Biotechnology, Brown University, Providence, RI 02912, USA

1Correspondence: Department of Pathology, Brown University School of Medicine, 164 Summit Ave., Providence, RI 02906, USA. E-mail: herman_vandenburgh{at}brown.edu

Space travel causes rapid and pronounced skeletal muscle wasting in humans that reduces their long-term flight capabilities. To develop effective countermeasures, the basis of this atrophy needs to be better understood. Space travel may cause muscle atrophy indirectly by altering circulating levels of factors such as growth hormone, glucocorticoids, and anabolic steroids and/or by a direct effect on the muscle fibers themselves. To determine whether skeletal muscle cells are directly affected by space travel, tissue-cultured avian skeletal muscle cells were tissue engineered into bioartificial muscles and flown in perfusion bioreactors for 9 to 10 days aboard the Space Transportation System (STS, i.e., Space Shuttle). Significant muscle fiber atrophy occurred due to a decrease in protein synthesis rates without alterations in protein degradation. Return of the muscle cells to Earth stimulated protein synthesis rates of both muscle-specific and extracellular matrix proteins relative to ground controls. These results show for the first time that skeletal muscle fibers are directly responsive to space travel and should be a target for countermeasure development.—Vandenburgh, H., Chromiak, J., Shansky, J., Del Tatto, M., Lemaire, J. Space travel directly induces skeletal muscle atrophy.


Key Words: protein turnover • skeletal myofiber • spaceflight • TCA




This article has been cited by other articles:


Home page
Am. J. Pathol.Home page
J. Naderi, C. Bernreuther, N. Grabinski, C. T. Putman, B. Henkel, G. Bell, M. Glatzel, and K. R. Sultan
Plasminogen Activator Inhibitor Type 1 Up-Regulation Is Associated with Skeletal Muscle Atrophy and Associated Fibrosis
Am. J. Pathol., August 1, 2009; 175(2): 763 - 771.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
N. Kim, C. M. Dempsey, C.-J. Kuan, J. V. Zoval, E. O'Rourke, G. Ruvkun, M. J. Madou, and J. Y. Sze
Gravity Force Transduced by the MEC-4/MEC-10 DEG/ENaC Channel Modulates DAF-16/FoxO Activity in Caenorhabditis elegans
Genetics, October 1, 2007; 177(2): 835 - 845.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
A. Higashibata, N. J. Szewczyk, C. A. Conley, M. Imamizo-Sato, A. Higashitani, and N. Ishioka
Decreased expression of myogenic transcription factors and myosin heavy chains in Caenorhabditis elegans muscles developed during spaceflight
J. Exp. Biol., August 15, 2006; 209(16): 3209 - 3218.
[Abstract] [Full Text] [PDF]


Home page
Aesthetic Surgery JournalHome page
C. L. DeLorenzi
Barbed Sutures: Rationale and Technique
Aesthetic Surgery Journal, March 1, 2006; 26(2): 223 - 229.
[Abstract] [Full Text] [PDF]


Home page
J BiochemHome page
Y. Seo, K. Lee, K. Park, K. Bae, and I. Choi
A Proteomic Assessment of Muscle Contractile Alterations during Unloading and Reloading
J. Biochem., January 1, 2006; 139(1): 71 - 80.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
F. H. Silver, D. DeVore, and L. M. Siperko
Invited Review: Role of mechanophysiology in aging of ECM: effects of changes in mechanochemical transduction
J Appl Physiol, November 1, 2003; 95(5): 2134 - 2141.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
N. J. Hudson and C. E. Franklin
Maintaining muscle mass during extended disuse: aestivating frogs as a model species
J. Exp. Biol., August 1, 2002; 205(15): 2297 - 2303.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
M. D. Grounds, J. D. White, N. Rosenthal, and M. A. Bogoyevitch
The Role of Stem Cells in Skeletal and Cardiac Muscle Repair
J. Histochem. Cytochem., May 1, 2002; 50(5): 589 - 610.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. G. Dennis, P. E. Kosnik II, M. E. Gilbert, and J. A. Faulkner
Excitability and contractility of skeletal muscle engineered from primary cultures and cell lines
Am J Physiol Cell Physiol, February 1, 2001; 280(2): C288 - C295.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
C. A. Ray
Interaction between vestibulosympathetic and skeletal muscle reflexes on sympathetic activity in humans
J Appl Physiol, January 1, 2001; 90(1): 242 - 247.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
W. Becker, J. Marxen, M. Epple, and O. Reelsen
Influence of microgravity on crystal formation in biomineralization
J Appl Physiol, October 1, 2000; 89(4): 1601 - 1607.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by The Federation of American Societies for Experimental Biology.