Skeletal muscle and peripheral nerve regenerate more poorly in old than in young rats. On the basis of data obtained from cross-age grafting models, an age-related change in the host appears to impair the capacity of muscle and nerve to regenerate.
The Specific Aims of this Program Project are to test four Group Hypotheses that in old as compared with young rats: A. poor regeneration of muscle grafts is related to deficient reinnervation; B. no structural or functional differences exist in muscle fibers during an early preinnervation stage, but structure and function of muscle fibers and motor units are impaired during a postinnervation stage; C. impaired axonal regeneration is related to defects in neuronal gene expression, myelin clearance, and macrophage and Schwann cell function; and D. cross-age nerve grafts ultimately become adapted to characteristics of the host. Hypotheses A and B will be tested by physiological analysis of single muscle fiber, motor unit and whole muscle properties, histochemistry and nerve staining, and electron microscopy. Hypotheses C and D will be tested by immunocytochemistry, in situ hybridization, morphometric analysis, autoradiography, growth factor analysis and Northern and Western blotting. The significance of the proposed research is the clarification of the mechanisms responsible for the improvement of muscle and nerve regeneration in old animals. The long-term goal of this research is to provide the basis for improving the repair of damaged muscle and nerve in old individuals.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
1P01AG010821-01
Application #
3091375
Study Section
Neuroscience, Behavior and Sociology of Aging Review Committee (NBSA)
Project Start
1993-01-01
Project End
1997-12-31
Budget Start
1993-01-01
Budget End
1993-12-31
Support Year
1
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Kung, Theodore A; Cederna, Paul S; van der Meulen, Jack H et al. (2014) Motor unit changes seen with skeletal muscle sarcopenia in oldest old rats. J Gerontol A Biol Sci Med Sci 69:657-65
Dow, Douglas E; Cederna, Paul S; Hassett, Cheryl A et al. (2007) Electrical stimulation prior to delayed reinnervation does not enhance recovery in muscles of rats. Restor Neurol Neurosci 25:601-10
Dow, Douglas E; Carlson, Bruce M; Hassett, Cheryl A et al. (2006) Electrical stimulation of denervated muscles of rats maintains mass and force, but not recovery following grafting. Restor Neurol Neurosci 24:41-54
Dow, Douglas E; Dennis, Robert G; Faulkner, John A (2005) Electrical stimulation attenuates denervation and age-related atrophy in extensor digitorum longus muscles of old rats. J Gerontol A Biol Sci Med Sci 60:416-24
Borisov, Andrei B; Dedkov, Eduard I; Carlson, Bruce M (2005) Abortive myogenesis in denervated skeletal muscle: differentiative properties of satellite cells, their migration, and block of terminal differentiation. Anat Embryol (Berl) 209:269-79
Borisov, Andrei B; Dedkov, Eduard I; Carlson, Bruce M (2005) Differentiation of activated satellite cells in denervated muscle following single fusions in situ and in cell culture. Histochem Cell Biol 124:13-23
Dow, Douglas E; Faulkner, John A; Dennis, Robert G (2005) Distribution of rest periods between electrically generated contractions in denervated muscles of rats. Artif Organs 29:432-5
Dow, Douglas E; Cederna, Paul S; Hassett, Cheryl A et al. (2004) Number of contractions to maintain mass and force of a denervated rat muscle. Muscle Nerve 30:77-86
Pan, Jie; Ruest, Louis-Bruno; Xu, Suying et al. (2004) Immuno-characterization of the switch of peptide elongation factors eEF1A-1/EF-1alpha and eEF1A-2/S1 in the central nervous system during mouse development. Brain Res Dev Brain Res 149:1-8
Dedkov, Eduard I; Borisov, Andrei B; Wernig, Anton et al. (2003) Aging of skeletal muscle does not affect the response of satellite cells to denervation. J Histochem Cytochem 51:853-63

Showing the most recent 10 out of 47 publications