Alzheimer's disease (AD) is a devastating neurodegenerative disease, characterized by beta amyloid, tau pathology and irreversible cognitive loss. Neither clear understanding of the pathological process nor the effective treatment of AD is available at present. Recent research indicates that increased endoplasmic reticulum (ER) calcium release from IP3R and ryanodine (RyR) calcium channels precedes amyloid deposition, tau pathology, neuronal loss, and cognitive impairments in AD. Targeting these early pathogenic processes may prove to be a successful therapeutic strategy of AD. Excessive calcium release from IP3R and hyperphosphorylation of tau via GSK3b upregulation is stabilized by lithium. RyR increases calcium release and impaired synaptic plasticity is stabilized by dantrolene, a novel RyR-channel stabilizer. The purpose of this project is to explore the role of IP3R and GSk3b and that of RyR-mediated calcium increase in synaptic dysfunction and AD pathological process and whether lithium and dantrolene derivatives can stabilize ER calcium channels and block synaptic dysfunction and AD pathology by pursuing two objectives below. Objective 1: Demonstrate that lithium serves as a neuroprotective agent during early stage of AD pathogenesis. We will treat AD mouse models (3xTg-AD) and controls with lithium for 4 weeks, and then examine biochemical changes indicative of histopathological cascades of AD, hippocampal synaptic integrity and also examine hippocampal synaptic plasticity and restoration of calcium signaling in CA1 hippocampal neurons. Objective 2: Examine whether dantrolene derivatives block impaired synaptic function and integrity. We will treat 3xTg-AD and control mice with the derivatives for 4 weeks, and then examine synaptic plasticity and integrity and restoration of calcium signaling in CA1 hippocampal neurons. This project could open a pathway to the development of an effective treatment of veterans with AD.

Public Health Relevance

Alzheimer's disease (AD) is one of the most common diseases faced by elderly veterans. The number of veterans with AD is estimated over 528,000 (FY06 demographic national survey). Only 136,000 veterans receive VA health care. The most serious problem in caring these veterans is that there are no drugs efficacious in treating AD. Previous research has long been focused on the final stages of pathological process of AD and has failed to develop an effective treatment strategy. Recent studies suggest that targeting the early pathogenic processes of AD has a great potential to develop the effective treatment of AD. This study focuses on this early pathogenic process of AD. The study will contribute to developing a novel therapeutic strategy for veterans with AD and improving the quality of life for those veterans.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Veterans Administration (I21)
Project #
1I21BX002462-01A1
Application #
8733390
Study Section
Neurobiology D (NURD)
Project Start
2014-10-01
Project End
2016-09-30
Budget Start
2014-10-01
Budget End
2015-09-30
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Edward Hines Jr VA Hospital
Department
Type
DUNS #
067445429
City
Hines
State
IL
Country
United States
Zip Code
60141
de Oliveira, Adriano Bof; Beck, Johannes; Daniels, Jörg et al. (2014) 4-Hy-droxy-3-meth-oxy-benzaldehyde 4-ethyl-thio-semicarbazone. Acta Crystallogr Sect E Struct Rep Online 70:o868