application): This program project has a long tradition of maintaining aging colonies of rodents under well- defined, barrier conditions. The animal core will continue this tradition by providing investigators in the projects and cores with healthy and well-defined colonies of aging transgenic and non-transgenic mice fed ad libitum and 60% ad libitum (dietary restriction, DR). Three transgenic mouse models will be maintained in the animal core: (1) DNA polymerase p heterozygous (p-po1 -/+) knockout mice, (2) transgenic mice over expressing the GLUT-4 glucose transporter protein, and (3) null CRH (corticosterone releasing hormone) knockout mice, as well as mice giving corticosterone supplementation. In addition, the animal core will maintain transgenic mice produced by the developmental core (Core D), in which the expression of genes are temporally regulated.
The specific aims of the animal core are as follows: (1) to maintain breeding colonies of the transgenic mice to produce the male transgenic mice used in this study by the three projects and core D. (2) To maintain aging colonies of transgenic and non-transgenic mice fed either ad libitum or a DR-diet. Animals from these colonies will be used by the investigators in three projects and core D for the experiments described in this proposal. (3) To maintain an aging colony of mice given corticosterone in their drinking water or given plain water for project 3. (4) to determine the survival of the transgenic and non-transgenic mice in the aging colonies described above and to provide the pathology Core (core C) with animals that die spontaneously in these colonies.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG014674-03
Application #
6314007
Study Section
Project Start
2000-05-15
Project End
2001-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
3
Fiscal Year
2000
Total Cost
$188,584
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Type
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Han, Eun-Soo; Muller, Florian L; Perez, Viviana I et al. (2008) The in vivo gene expression signature of oxidative stress. Physiol Genomics 34:112-26
McCarter, Roger; Mejia, Walter; Ikeno, Yuji et al. (2007) Plasma glucose and the action of calorie restriction on aging. J Gerontol A Biol Sci Med Sci 62:1059-70
Cabelof, Diane C; Ikeno, Yuji; Nyska, Abraham et al. (2006) Haploinsufficiency in DNA polymerase beta increases cancer risk with age and alters mortality rate. Cancer Res 66:7460-5
Fu, Chunxiao; Hickey, Morgen; Morrison, Melissa et al. (2006) Tissue specific and non-specific changes in gene expression by aging and by early stage CR. Mech Ageing Dev 127:905-16
Sharp, Zelton Dave; Bartke, Andrzej (2005) Evidence for down-regulation of phosphoinositide 3-kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR)-dependent translation regulatory signaling pathways in Ames dwarf mice. J Gerontol A Biol Sci Med Sci 60:293-300
Han, Eun-Soo; Hickey, Morgen (2005) Microarray evaluation of dietary restriction. J Nutr 135:1343-6
Street, K A; Xu, G; Hall, K L et al. (2005) Rat synapsin 1 promoter mediated transgene expression in testicular cell types. DNA Cell Biol 24:133-40
Muller, Florian L; Liu, Yuhong; Van Remmen, Holly (2004) Complex III releases superoxide to both sides of the inner mitochondrial membrane. J Biol Chem 279:49064-73
Chen, Xinlian; Liang, Hanyu; Van Remmen, Holly et al. (2004) Catalase transgenic mice: characterization and sensitivity to oxidative stress. Arch Biochem Biophys 422:197-210
Cook, Peyton; Fu, Chunxiao; Hickey, Morgen et al. (2004) SAS programs for real-time RT-PCR having multiple independent samples. Biotechniques 37:990-5

Showing the most recent 10 out of 33 publications