Our interest in cardiac EC's stem from the fact that cardiovascular disease continues to be a major health problem in our society. We believe that release of factors from cardiac coronary EC's which participate in the regulation of regional blood flow may have a role in normal cardiac function and in cardiovascular disease. It has been demonstrated that endothelial cells (EC's) release adenosine 5'-triphosphate (ATP) and autocoids outside the cell in response to various stimuli. It has been suggested that ATP release from these cells is receptor-mediated. It is possible that the P2/y receptor plays a role in mediating the ATP release. We want to test the hypothesis that cardiac EC release of ATP in response to agonists occurs both luminally and abluminally and test the effect of hypoxia and re-oxygenation on this process. We will utilize permeable membranes to primary cultures of EC's. This design is a paradigm of the in vivo situation defining apical versus basolateral compartments. Both enzyme luminescence assays and high-pressure liquid chromatography techniques will be used to measure ATP release from EC'S. We will also test the hypothesis that the release of ATP is associated with the release of nitric oxide (NO). Enzyme luminescence assays will be used to measure NO as well. We will administer both agonist and antagonists to ATP and NO release and evaluate any alterations in the respective releases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Nursing Research (NINR)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31NR007379-05
Application #
6529262
Study Section
National Institute of Nursing Research Initial Review Group (NRRC)
Program Officer
Armstrong, Nell
Project Start
2002-08-01
Project End
Budget Start
2002-08-01
Budget End
2003-01-31
Support Year
5
Fiscal Year
2002
Total Cost
$12,398
Indirect Cost
Name
University of Nevada Reno
Department
Pharmacology
Type
Schools of Medicine
DUNS #
146515460
City
Reno
State
NV
Country
United States
Zip Code
89557
Oxhorn, Brian C; Sanguinetti, Amy R; Mastick, Cynthia Corley et al. (2005) c-Abl is required for staurosporine-induced caspase activity. Proc West Pharmacol Soc 48:110-7
Oxhorn, Brian C; Buxton, Iain L O (2003) Caveolar compartmentation of caspase-3 in cardiac endothelial cells. Cell Signal 15:489-96
Oxhorn, Brian C; Hirzel, Douglas J; Buxton, Iain L O (2002) Isolation and characterization of large numbers of endothelial cells for studies of cell signaling. Microvasc Res 64:302-15
Oxhorn, B C; Wadia, R; Buxton, I L (2001) Caspase-3 is localized to endothelial caveolar domains. Proc West Pharmacol Soc 44:45-8
Buxton, I L; Kaiser, R A; Oxhorn, B C et al. (2001) Evidence supporting the Nucleotide Axis Hypothesis: ATP release and metabolism by coronary endothelium. Am J Physiol Heart Circ Physiol 281:H1657-66