The Program Project is focused on the bases for individual differences in cognitive decline and brain aging in hippocampal/cortical systems. The primary subjects are pathogen-free male Long-Evans rats, with some additional work using non-human primates to provide a cross-species comparison. The participating investigators will deploy their expertise in anatomical, electrophysiological and molecular biological studies of the hippocampus, a system that also supports cognitive functions in the human brain. An important feature of the research program is the use of brain material from a common source that provides standardized assessments of cognitive function (Animal Resource Core) for the neurobiological studies. A centralized Data Management component of the Core is designed to facilitate within-project and across-project analyses. The five individual projects will focus on four main program objectives. The first objective will compare vulnerability of cortical and subcortical neurons associated with the hippocampal formation, where we have found substantially preserved numbers of neurons, irrespective of age or behavioral status. A third program objective is to examine functional alterations for information encoding, signal transduction, and neural plasticity in the hippocampus and the relation of such changes to hippocampal-dependent cognitive decline. Finally, a fourth program objective is to test specific hypotheses about causes of hippocampal aging. The concept that exposure to oxidative stress is a contributing factor. Our approach has significant potential for increasing our understanding of the aging process and for assessing the therapeutic potential of specific neurobiological interventions.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
3P01AG009973-09S1
Application #
6153302
Study Section
Special Emphasis Panel (ZAG1 (90))
Project Start
1991-08-01
Project End
2001-07-31
Budget Start
1999-09-30
Budget End
2000-08-31
Support Year
9
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Haberman, Rebecca P; Koh, Ming Teng; Gallagher, Michela (2017) Heightened cortical excitability in aged rodents with memory impairment. Neurobiol Aging 54:144-151
Haberman, Rebecca P; Branch, Audrey; Gallagher, Michela (2017) Targeting Neural Hyperactivity as a Treatment to Stem Progression of Late-Onset Alzheimer's Disease. Neurotherapeutics 14:662-676
Posada-Duque, Rafael Andrés; Ramirez, Omar; Härtel, Steffen et al. (2017) CDK5 downregulation enhances synaptic plasticity. Cell Mol Life Sci 74:153-172
Gu, Yu; Tran, Trinh; Murase, Sachiko et al. (2016) Neuregulin-Dependent Regulation of Fast-Spiking Interneuron Excitability Controls the Timing of the Critical Period. J Neurosci 36:10285-10295
Wang, Hui; Ardiles, Alvaro O; Yang, Sunggu et al. (2016) Metabotropic Glutamate Receptors Induce a Form of LTP Controlled by Translation and Arc Signaling in the Hippocampus. J Neurosci 36:1723-9
Robitsek, Jonathan; Ratner, Marcia H; Stewart, Tara et al. (2015) Combined administration of levetiracetam and valproic acid attenuates age-related hyperactivity of CA3 place cells, reduces place field area, and increases spatial information content in aged rat hippocampus. Hippocampus 25:1541-55
Tomás Pereira, Inês; Gallagher, Michela; Rapp, Peter R (2015) Head west or left, east or right: interactions between memory systems in neurocognitive aging. Neurobiol Aging 36:3067-3078
Gallagher, Michela; Burwell, Rebecca; Burchinal, Margaret (2015) Severity of spatial learning impairment in aging: Development of a learning index for performance in the Morris water maze. Behav Neurosci 129:540-8
Mayse, Jeffrey D; Nelson, Geoffrey M; Avila, Irene et al. (2015) Basal forebrain neuronal inhibition enables rapid behavioral stopping. Nat Neurosci 18:1501-8
Koh, Ming Teng; Spiegel, Amy M; Gallagher, Michela (2014) Age-associated changes in hippocampal-dependent cognition in Diversity Outbred mice. Hippocampus 24:1300-7

Showing the most recent 10 out of 165 publications