Core C is essential component of the Gene Action Program Project which has always placed a high priority on analysis of aging effects on animal model systems. This tradition continues with a restructured emphasis oriented toward transgenic mice which overexpress genes which may influence the accumulative and composite effects of oxidative injury to nuclear and mitochondrial DNA. Core C will accomplish two major goals which will support each of the primary projects. The first goal is to provide transgenic and control mice which are maintained in a rigorous manner necessary to limit the influence of complicating factors such as intercurrent disease and nutrition on the aging process. This is supported by the first specific aim which is to provide breeding management and husbandry conditions necessary for the propagation of healthy and well- defined transgenic and control animals required by the projects and cores. The second goal is to provide an in-life and post-mortem analysis of transgenic and control mice throughout their natural lifespans. The second and third specific aims support this goal by (Aim 2) assessing the neurobehavioral influences of aging in transgenic and control mice during their natural lifespan, and (Aim 3) by establishing a reproductive and life table analysis and assessing the pathologic consequence of aging in transgenic and control mice during their natural lifespan. Accomplishment of these goals will permit associations to be developed between experimental observations made within individual projects and their ultimate expression in a integrated whole animal system.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG001751-20
Application #
6097927
Study Section
Project Start
1998-08-01
Project End
1999-07-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
20
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Basisty, Nathan B; Liu, Yuxin; Reynolds, Jason et al. (2018) Stable Isotope Labeling Reveals Novel Insights Into Ubiquitin-Mediated Protein Aggregation With Age, Calorie Restriction, and Rapamycin Treatment. J Gerontol A Biol Sci Med Sci 73:561-570
Kramer, Philip A; Duan, Jicheng; Gaffrey, Matthew J et al. (2018) Fatiguing contractions increase protein S-glutathionylation occupancy in mouse skeletal muscle. Redox Biol 17:367-376
Zhang, Huiliang; Gong, Guohua; Wang, Pei et al. (2018) Heart specific knockout of Ndufs4 ameliorates ischemia reperfusion injury. J Mol Cell Cardiol 123:38-45
Ge, Xuan; Ciol, Marcia A; Pettan-Brewer, Christina et al. (2017) Self-motivated and stress-response performance assays in mice are age-dependent. Exp Gerontol 91:1-4
Sweetwyne, Mariya T; Pippin, Jeffrey W; Eng, Diana G et al. (2017) The mitochondrial-targeted peptide, SS-31, improves glomerular architecture in mice of advanced age. Kidney Int 91:1126-1145
Liu, Sophia Z; Marcinek, David J (2017) Skeletal muscle bioenergetics in aging and heart failure. Heart Fail Rev 22:167-178
Kruse, Shane E; Karunadharma, Pabalu P; Basisty, Nathan et al. (2016) Age modifies respiratory complex I and protein homeostasis in a muscle type-specific manner. Aging Cell 15:89-99
Loeb, Lawrence A (2016) Human Cancers Express a Mutator Phenotype: Hypothesis, Origin, and Consequences. Cancer Res 76:2057-9
Chiao, Ying Ann; Kolwicz, Stephen C; Basisty, Nathan et al. (2016) Rapamycin transiently induces mitochondrial remodeling to reprogram energy metabolism in old hearts. Aging (Albany NY) 8:314-27
Campbell, Matthew D; Marcinek, David J (2016) Evaluation of in vivo mitochondrial bioenergetics in skeletal muscle using NMR and optical methods. Biochim Biophys Acta 1862:716-724

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