The goal of the Animal Core is to provide support for each of the projects funded in the Program Project. In addition to standard responsibilities currently in progress, the Core will assume an additional responsibility to develop a colony of animals with the Tgr mutation (rGHRH-hGH) in a Brown-Norway genetic background. This will include characterizing the transgenic animal model for aging studies and detailing the basic characteristics of adult onset growth hormone deficiency in transgenics as compared to wild-type animals. This will be accomplished by infusing growth hormone-releasing hormone (GHRH) into the Tgr rat to ensure similar growth characteristics compared to wild-type animals. Growth hormone deficiency will then be induced in adulthood by withdrawal of GHRH infusion. We propose that growth hormone deficiency induced in adulthood will result in alterations in a number of parameters associated with age including, but not limited to, a decrease in plasma IGF-1 levels. rarefaction of brain vasculature, synaptic loss, alterations in axonal and dendritic architecture, and cognitive deficits. Specific aspects of adult- onset growth hormone deficiency using these animals will be assessed by the individual projects. The Animal Core has multiple aims. 1) The Core will procure and maintain animals used by program investigators and meet all AAALAC and institutional standards for animal care in the satellite facilities. The Core also has the responsibility of implanting animals with intracerebroventricular cannulae with osmotic mini-pumps for short- term (28 days) administration of IGF-1. 2) The core personnel will assess basic parameters of aging animals (general health and body weight), monitor sentinel and experimental animals for presence of disease and provide these data to project investigators. 3) The Core will develop a model for adult-onset growth hormone deficiency. Initial studies will validate the utility of the Tgr (Transgenic growth retarded) rat as a model appropriate to study brain aging. 4) The Core will provide statistical support for collaboration in the design of studies, data management, and statistical analyses of within project and between project results. The Animal Core is an essential aspect of the Program Project ensuring effective management of limited resources, smooth interactions between projects and the use of animal models that have been validated for studies of the biology of aging. In addition, the Core will be responsible for facilitating interactions with external/internal consultants and assisting in maintaining the focus of individual projects and the overall program.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG011370-07
Application #
6430835
Study Section
Project Start
2001-04-01
Project End
2003-03-31
Budget Start
Budget End
Support Year
7
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Type
DUNS #
041418799
City
Winston-Salem
State
NC
Country
United States
Zip Code
27106
Luo, T David; Alton, Timothy B; Apel, Peter J et al. (2016) Effects of age and insulin-like growth factor-1 on rat neurotrophin receptor expression after nerve injury. Muscle Nerve 54:769-75
Tucsek, Zsuzsanna; Toth, Peter; Sosnowska, Danuta et al. (2014) Obesity in aging exacerbates blood-brain barrier disruption, neuroinflammation, and oxidative stress in the mouse hippocampus: effects on expression of genes involved in beta-amyloid generation and Alzheimer's disease. J Gerontol A Biol Sci Med Sci 69:1212-26
Masser, Dustin R; Bixler, Georgina V; Brucklacher, Robert M et al. (2014) Hippocampal subregions exhibit both distinct and shared transcriptomic responses to aging and nonneurodegenerative cognitive decline. J Gerontol A Biol Sci Med Sci 69:1311-24
Sosnowska, Danuta; Richardson, Chris; Sonntag, William E et al. (2014) A heart that beats for 500 years: age-related changes in cardiac proteasome activity, oxidative protein damage and expression of heat shock proteins, inflammatory factors, and mitochondrial complexes in Arctica islandica, the longest-living noncolonial an J Gerontol A Biol Sci Med Sci 69:1448-61
Toth, Peter; Tarantini, Stefano; Tucsek, Zsuzsanna et al. (2014) Resveratrol treatment rescues neurovascular coupling in aged mice: role of improved cerebromicrovascular endothelial function and downregulation of NADPH oxidase. Am J Physiol Heart Circ Physiol 306:H299-308
Csiszar, Anna; Gautam, Tripti; Sosnowska, Danuta et al. (2014) Caloric restriction confers persistent anti-oxidative, pro-angiogenic, and anti-inflammatory effects and promotes anti-aging miRNA expression profile in cerebromicrovascular endothelial cells of aged rats. Am J Physiol Heart Circ Physiol 307:H292-306
Bailey-Downs, Lora C; Tucsek, Zsuzsanna; Toth, Peter et al. (2013) Aging exacerbates obesity-induced oxidative stress and inflammation in perivascular adipose tissue in mice: a paracrine mechanism contributing to vascular redox dysregulation and inflammation. J Gerontol A Biol Sci Med Sci 68:780-92
Warrington, Junie P; Ashpole, Nicole; Csiszar, Anna et al. (2013) Whole brain radiation-induced vascular cognitive impairment: mechanisms and implications. J Vasc Res 50:445-57
Ungvari, Zoltan; Podlutsky, Andrej; Sosnowska, Danuta et al. (2013) Ionizing radiation promotes the acquisition of a senescence-associated secretory phenotype and impairs angiogenic capacity in cerebromicrovascular endothelial cells: role of increased DNA damage and decreased DNA repair capacity in microvascular radiosens J Gerontol A Biol Sci Med Sci 68:1443-57
Ungvari, Zoltan; Csiszar, Anna; Sosnowska, Danuta et al. (2013) Testing predictions of the oxidative stress hypothesis of aging using a novel invertebrate model of longevity: the giant clam (Tridacna derasa). J Gerontol A Biol Sci Med Sci 68:359-67

Showing the most recent 10 out of 131 publications