The natural process of aging is also the leading risk factor for Alzheimer?s disease (AD), a prevalent form of dementia that has devastating effects on the quality of human life and health care costs. As cognitive functions progressively deteriorate with AD, a neurobiological understanding of how AD alters brain cells and their circuit functions is one of the great challenges facing modern biomedical research with broad implications for advancing the nation?s health as well as stimulating the economy. Considerable human and animal AD research has focused on relating ?physical? (macroscopic, microscopic) changes in the brain with destructive loss of memory (i.e., anterograde and retrograde amnesias). In contrast, significantly less is known about the impact of AD on other cognitive functioning, such as risky decision-making which plays pervasive role in daily life, and how AD-afflicted neurons operate in ?real-time? as cognitive functioning is taking place. The primary goal of this application is to understand the dynamics of prelimbic cortex-hippocampus (PL-HPC) circuit functions in decision-making in a murine model of AD, utilizing an ecologically-relevant behavioral paradigm. We will test the general hypothesis that AD causes coordinated PL-HPC neural activities and risky decision- making abilities to decline as a function of the amyloid plaque accumulation in the two structures. There are two specific aims of the project: (1) an ETHOBEHAVIORAL ANALYSIS will investigate the scope of amyloid plaque effects on the animal?s ability to discern safety-danger boundary and make optimal risky foraging decisions; and (2) a SYSTEMS-LEVEL ANALYSIS will determine the neural synchrony in the PL-HPC network as AD mice perform risky foraging and also probe whether decision-making deficits can be alleviated by optogenetic intervention. Information generated from this project would be of significance (1) from a basic scientific perspective because it will provide novel data pertaining to AD-associated changes neural coding and decision-making; and (2) from an applied perspective because it provides a new avenue of naturalistic-based preclinical research that can potentially lead to developing successful treatments of AD-related declines in cognitive functions.

Public Health Relevance

While much research on Alzheimer?s disease (AD) has focused on ?physical? neuropathological markers (i.e., plaques and tangles) in the brain and consequent loss of memory functions, there is very limited information as to how AD adversely affects brain cell activities in ?real-time? during cognitive functions. Thus, this project will investigate how the neural coding in the cortico-limbic (i.e., prelimbic cortex-hippocampus) network, which plays important role in risky decision-making, is altered by amyloid pathology in a well-characterized AD mouse model (i.e. 5XFAD). Data generated from this project will fill important gaps in the AD field, stimulate future research, and provide deeper insights into understanding this devastating neurodegenerative disease that profoundly impact the quality of human life and the nation?s economy in today?s increasingly long-living society.

National Institute of Health (NIH)
National Institute on Aging (NIA)
Exploratory/Developmental Grants (R21)
Project #
Application #
Study Section
Biobehavioral Regulation, Learning and Ethology Study Section (BRLE)
Program Officer
Wagster, Molly V
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Washington
Schools of Arts and Sciences
United States
Zip Code