Project 2: Analysis of Skeletal Muscle Function in Aging Mice. The purpose of this project is to provide measurements of age-sensitive traits from skeletal muscles of mice for studies of genetic linkage and biomarker validation and to investigate metabolic mechanisms underlying the increased fatiguability of muscles in old mice. The Program Project primary addresses Program-wide working hypotheses that direct studies to seek evidence for (i) correlations across organ systems in the extent of the accumulation of age-related changes, and (ii) the existence of polymorphic genetic loci that lead to relatively rapid aging. Deficits observed in skeletal in skeletal muscles of aging mice include decreases in mass, maximum isometric force, and resistance to fatigue. Project 2 will contribute to the overall goals of the Program Project, by providing structural, functional, and metabolic data from skeletal muscles of genetically heterogeneous female mice. These data will be examined by the Data Analysis Core along with data from the other Projects and the genotypic information from each mouse to test rigorously the Program's working hypotheses. In addition, Project 2 has aims related to our own interests in the biology of skeletal muscles in aging animals. Increased fatiguability is one of the primary contributors to physical frailty in the elderly. The fatiguability of individual skeletal muscle is assessed through measurements of sustained power during prolonged contractile activity. The ability of muscles in old animals to sustain power is significantly impaired compared with that of muscles in young animals. Mechanisms underlying these functional deficits have not been studied in aging mice. The working hypothesis is that the decreased ability of isolated muscles in old mice to sustain power during repeated contractions is due to altered substrate utilization. The large data sets generated by Project 2 will be used to seek relationships between the ability of a muscle to sustain power during contractile activity, the ability of the muscle to utilize substrates, and the animal;s level of voluntary activity. The development of these relationships will contribute significantly to our understanding of the increasing physical frailty observed with aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG016699-02
Application #
6325718
Study Section
Project Start
2000-07-01
Project End
2001-04-30
Budget Start
Budget End
Support Year
2
Fiscal Year
2000
Total Cost
$100,786
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Burke, David T; Kozloff, Kenneth M; Chen, Shu et al. (2012) Dissection of complex adult traits in a mouse synthetic population. Genome Res 22:1549-57
Chisa, Jennifer L; Burke, David T (2007) Mammalian mRNA splice-isoform selection is tightly controlled. Genetics 175:1079-87
Hanlon, Philip; Lorenz, William Andrew; Shao, Zhihong et al. (2006) Three-locus and four-locus QTL interactions influence mouse insulin-like growth factor-I. Physiol Genomics 26:46-54
Harper, James M; Salmon, Adam B; Chang, Yayi et al. (2006) Stress resistance and aging: influence of genes and nutrition. Mech Ageing Dev 127:687-94
Harper, James M; Durkee, Stephen J; Smith-Wheelock, Michael et al. (2005) Hyperglycemia, impaired glucose tolerance and elevated glycated hemoglobin levels in a long-lived mouse stock. Exp Gerontol 40:303-14
Wisser, Kathleen C; Schauerte, Joseph A; Burke, David T et al. (2004) Mapping tissue-specific genes correlated with age-dependent changes in protein stability and function. Arch Biochem Biophys 432:58-70
Volkman, Suzanne K; Galecki, Andrzej T; Burke, David T et al. (2004) Quantitative trait loci that modulate femoral mechanical properties in a genetically heterogeneous mouse population. J Bone Miner Res 19:1497-505
Harper, James M; Galecki, Andrzej T; Burke, David T et al. (2004) Body weight, hormones and T cell subsets as predictors of life span in genetically heterogeneous mice. Mech Ageing Dev 125:381-90
Harper, James M; Galecki, Andrzej T; Burke, David T et al. (2003) Quantitative trait loci for insulin-like growth factor I, leptin, thyroxine, and corticosterone in genetically heterogeneous mice. Physiol Genomics 15:44-51
Bennett-Baker, Pamela E; Wilkowski, Jodi; Burke, David T (2003) Age-associated activation of epigenetically repressed genes in the mouse. Genetics 165:2055-62

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