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Mechanical Signal Transduction in Countermeasures to Muscle AtrophyWe have shown that modifications in muscle use result in changes in the expression and activity of calpains and nitric oxide synthase (NOS). Although muscle unloading for 10 days produced no change in the concentrations of calpain 1 or 2 and no change in calpain activation, muscle reloading produced a 90% increase in calpain 2 concentration. We developed an in vitro model to test our hypothesis that nitric oxide can inhibit cytoskeletal breakdown in skeletal muscle cells by inhibiting calpain cleavage of talin. Talin was selected because it is a well-characterized calpain substrate and it is codistributed with calpain in muscle cells. We found that intermittant loading during hindlimb suspension that is sufficient to prevent muscle mass loss that occurs during muscle unloading is also sufficient to prevent the decrease in NOS expression that normally occurs during hindlimb unloading. These findings indicate that therapeutics directed toward regulating the calpain/calpastatin system may be beneficial in preventing muscle mass loss in muscle injury, unloading and disease.
Document ID
20020065430
Document Type
Other
Authors
Tidball, James G. (California Univ. Los Angeles, CA United States)
Chu, Amy
Date Acquired
September 7, 2013
Publication Date
January 1, 2002
Subject Category
Aerospace Medicine
Funding Number(s)
CONTRACT_GRANT: NAG2-1193
Distribution Limits
Public
Copyright
Work of the US Gov. Public Use Permitted.

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