This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This project will define the significance of secretory phospholipases A2 (sPLA2s) in neuronal signaling and injury. Two major goals of this project are to: 1) define how lipid messengers generated by sPLA2s modulate neuronal survival and function, and 2) to identify gene expression in the brain, modulated by sPLA2(s). We have shown that sPLA2s alter neuronal survival and function in vitro and in vivo. We have demonstrated effects of sPLA2s on neuronal calcium homeostasis and cell injury stimulated by glutamate. It is our hypothesis that lipids generated by sPLA2 enzyme activity, such as arachidonic acid and platelet-activating factor, may modulate neuronal excitation at the synapse, and thus alter physiological and pathological outcomes in the brain. Here we will correlate effects at the cellular level with in vivo outcomes such as learning and memory, as well as cell injury in the brain. Arachidonic acid and PAF will be used directly, as well as purified sPLA2s, to modulate neuronal function. A second goal of this project is to identify alterations in gene expression caused by sPLA2s in the brain. This goal will be accomplished by utilizing the Molecular Neurobiology Core Module. Primary cultures of neurons and astrocytes will be ideal for this technology, as cultures under injury and stress conditions can be compared to determine which genes are upregulated. Brain tissue from experimental animals treated with sPLA2s, PAF, or arachidonic acid will also be used. Thus, the goal of determining the role of endogenous sPLA2 in neuronal function and injury will benefit from the Molecular Neurobiology Core Module.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR016816-08
Application #
7959416
Study Section
Special Emphasis Panel (ZRR1-RI-8 (01))
Project Start
2009-02-01
Project End
2010-01-31
Budget Start
2009-02-01
Budget End
2010-01-31
Support Year
8
Fiscal Year
2009
Total Cost
$190,312
Indirect Cost
Name
Louisiana State Univ Hsc New Orleans
Department
Neurology
Type
Schools of Medicine
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Ponnath, Abhilash; Farris, Hamilton E (2014) Sound-by-sound thalamic stimulation modulates midbrain auditory excitability and relative binaural sensitivity in frogs. Front Neural Circuits 8:85
Ferland, Chantelle L; Harris, Erin P; Lam, Mai et al. (2014) Facilitation of the HPA axis to a novel acute stress following chronic stress exposure modulates histone acetylation and the ERK/MAPK pathway in the dentate gyrus of male rats. Endocrinology 155:2942-52
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Ponnath, Abhilash; Hoke, Kim L; Farris, Hamilton E (2013) Stimulus change detection in phasic auditory units in the frog midbrain: frequency and ear specific adaptation. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 199:295-313
Imaizumi, Kazuo; Shih, Jonathan Y; Farris, Hamilton E (2013) Global hyper-synchronous spontaneous activity in the developing optic tectum. Sci Rep 3:1552
Jones, Patricia L; Farris, Hamilton E; Ryan, Michael J et al. (2013) Do frog-eating bats perceptually bind the complex components of frog calls? J Comp Physiol A Neuroethol Sens Neural Behav Physiol 199:279-83
Harrison, Laura M (2012) Rhes: a GTP-binding protein integral to striatal physiology and pathology. Cell Mol Neurobiol 32:907-18

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