Fetal alcohol syndrome and related disorders occur in approximately 1% of live births in the United States and represent the most common cause of mental retardation. Fetal alcohol syndrome is commonly associated with significant lifetime disability, and thus the prevention and treatment of this syndrome is greatly needed. Normally, microglia protect neurons through the production of neurotrophic factors. However, microglia are resident CNS macrophages which play a critical role in the innate immune response to pathogens. Ethanol causes activation of microglia which may contribute to neuropathogenesis. Toll-like receptors (TLRs) respond to pathogens and endogenous """"""""danger signals"""""""" produced following trauma or tissue injury. The mechanisms by which alcohol modulates microglia-neuronal interactions and neuropathogenesis in animal models of fetal alcohol syndrome have not been elucidated. The general hypothesis of the proposed studies is that TLRs expressed on microglia play a critical role in modulating ethanol induced neurodegeneration in the developing nervous system.
The Specific Aims of the proposed research are as follows:
f Specific Aim 1 : Determine the mechanisms by which microglial TLRs modulate response to alcohol and neurodegeneration. The effects of alcohol on TLR signaling pathways in vitro will be examined in primary microglia. The role of specific TLR signaling molecules will be assessed in these studies utilizing microglia derived from animals in which these molecules have been knocked out. Co-culture paradigms will be used to assess the role of TLRs in modulating alcohol effects on neuron viability.
f Specific Aim 2 : Determine the effects of TLRs in modulating neurodegeneration in vivo in animal models of fetal alcohol syndrome. The effects of ethanol on specific TLR signaling pathways will be evaluated in studies utilizing animals in which key TLR signaling molecules have been knocked out. We have demonstrated that specific nuclear receptor agonists alter TLR signaling in microglia. We will evaluate the therapeutic potential of these agonists in modulating alcohol induced neurodegeneration in our animal model of fetal alcohol syndrome. The proposed studies will determine the mechanisms by which TLRs expressed on microglia modulate alcohol induced neurodegeneration in the developing nervous system. These studies have important implications concerning the treatment of fetal alcohol syndrome.

Public Health Relevance

Fetal alcohol syndrome and related disorders occur in approximately 1% of live births in the United States and represent the most common non-genetic cause of mental retardation. Fetal alcohol syndrome is commonly associated with significant lifetime disability, and thus the prevention and treatment of this syndrome is greatly needed. The proposed studies are designed to evaluate the role of """"""""danger signals"""""""" produced following alcohol exposure to the developing brain, with the goal of developing future therapies for fetal alcohol syndrome.

Agency
National Institute of Health (NIH)
Institute
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AA018839-01
Application #
7798349
Study Section
Special Emphasis Panel (ZAA1-CC (03))
Program Officer
Regunathan, Soundar
Project Start
2009-09-30
Project End
2011-08-31
Budget Start
2009-09-30
Budget End
2010-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$217,500
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
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Kane, Cynthia J M; Phelan, Kevin D; Douglas, James C et al. (2014) Effects of ethanol on immune response in the brain: region-specific changes in adolescent versus adult mice. Alcohol Clin Exp Res 38:384-91
Drew, Paul D; Kane, Cynthia J M (2014) Fetal alcohol spectrum disorders and neuroimmune changes. Int Rev Neurobiol 118:41-80
Kane, Cynthia J M; Phelan, Kevin D; Douglas, James C et al. (2013) Effects of ethanol on immune response in the brain: region-specific changes in aged mice. J Neuroinflammation 10:66
Kane, Cynthia J M; Phelan, Kevin D; Drew, Paul D (2012) Neuroimmune mechanisms in fetal alcohol spectrum disorder. Dev Neurobiol 72:1302-16
Kane, Cynthia J M; Phelan, Kevin D; Han, Lihong et al. (2011) Protection of neurons and microglia against ethanol in a mouse model of fetal alcohol spectrum disorders by peroxisome proliferator-activated receptor-? agonists. Brain Behav Immun 25 Suppl 1:S137-45