Combined dopaminergic neurotoxicity of manganese and LPS
Project Number1R01ES013265-01
Contact PI/Project LeaderLIU, BIN
Awardee OrganizationUNIVERSITY OF FLORIDA
Description
Abstract Text
DESCRIPTION (provided by applicant): Parkinson's disease (PD) is a movement disorder characterized by a progressive and selective loss of dopamine (DA) neurons in the substantia nigra. At the present, PD affects nearly one million people in the US alone and the incidence is expected to increase with an aging population. The vast majority of PD is idiopathic, occurs late in life, and does not appear to be directly related to gene mutations identified in several familial clusters of early-onset PD. Accumulating evidence indicates that environmental agents including heavy metals and infectious agents represent risk factors for idiopathic PD. The DA neurotoxicity of the heavy metal manganese has been documented and activation of brain immune cells (microglia and astroglia) by bacterial endotoxin lipopolysaccharide (LPS) is known to releases neurotoxic factors to induce neurodegeneration. However, the etiology of PD may be multi-factorial: the development of PD may be a final outcome of chronic exposure to low concentrations of multiple environmental agents. Therefore, this proposal plans to study the combined DA neurotoxicity of low concentrations of the heavy metal manganese and LPS in a chronic primary neuron-gila culture-based model of PD. The mechanism of the combined neurotoxicity will be analyzed at both the cellular and molecular levels. At the cellular level, the relative contribution to the combined neurotoxicity of the primary brain immune cells, microglia, and astroglia will be determined. At the molecular levels, the contribution to neurodegeneration of neurotoxic factors (free radicals and cytokines) by activated gila and the mechanism of neurodegenerative process will be examined. The results of these studies will enable us to gain understanding of the impact of heavy metals and microbial toxins on the DA system. These studies will also be an important component of our long-term goal of understanding the interaction between environmental factors and the nervous system in relation to the etiology of PD and finding effective strategies for the prevention and/or treatment of the disease.
National Institute of Environmental Health Sciences
CFDA Code
113
DUNS Number
969663814
UEI
NNFQH1JAPEP3
Project Start Date
01-August-2004
Project End Date
30-April-2007
Budget Start Date
01-August-2004
Budget End Date
30-April-2005
Project Funding Information for 2004
Total Funding
$145,500
Direct Costs
$100,000
Indirect Costs
$45,500
Year
Funding IC
FY Total Cost by IC
2004
National Institute of Environmental Health Sciences
$145,500
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1R01ES013265-01
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 1R01ES013265-01
Patents
No Patents information available for 1R01ES013265-01
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 1R01ES013265-01
Clinical Studies
No Clinical Studies information available for 1R01ES013265-01
News and More
Related News Releases
No news release information available for 1R01ES013265-01
History
No Historical information available for 1R01ES013265-01
Similar Projects
No Similar Projects information available for 1R01ES013265-01