The major objective of this investigation will be to explore the biochemical mode(s) of action of the potent lipid biochemical mediator, acetylglyceryletherphosphorylcholine, AGEPC, in liver. This compound has been identified previously as """"""""platelet activating factor"""""""", released during systemic anaphylaxis in rabbits and now recognized as one of the most potent mediators implicated in acute allergic and inflammatory reactions. Recently our laboratories have observed that this compound exerts a profound activity on phosphoinositide metabolism and glucose release in liver preparations. The experimental approach to be employed in this study is best expressed in the following specific aims: I. To characterize at the enzymatic level the stimulatory effect of AGEPC on hepatic glygcogenolysis. II. To investigate the mechanism of the stimulatory effect of AGEPC on hepatic gluconeogenesis. III. To evaluate the relationship between the metabolic effects of AGEPC in the liver and alterations in the cellular calcium ion fluxes. IV. To examine and to compare the effects of AGEPC and other glycogenolytic hormones on the metabolism of phosphoinositides and other phospholipids in hepatocytes. V. To investigate the metabolic fate of AGEPC in the liver. VI. To determin whether the addition of glycogenolytic hormones to the liver results in the production of AGEPC or closely related derivative(s). VII. To characterize the receptor for AGEPC on hepatic cellular membranes. This project should provide new insights into the mechanism by which this unusual phospholipid and its analogues exert their activity towards a non-inflammatory cell, in this instance, and hopefully will develop as a model for inquiry into the mode of action of AGEPC in other tissues and cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK033538-05
Application #
3231954
Study Section
Biochemistry Study Section (BIO)
Project Start
1984-04-01
Project End
1989-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
5
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Type
School of Medicine & Dentistry
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
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Svetlov, S I; Sturm, E; Olson, M S et al. (1999) Hepatic regulation of platelet-activating factor acetylhydrolase and lecithin:cholesterol acyltransferase biliary and plasma output in rats exposed to bacterial lipopolysaccharide. Hepatology 30:128-36
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Mustafa, S B; Flickinger, B D; Olson, M S (1999) Suppression of lipopolysaccharide-induced nitric oxide synthase expression by platelet-activating factor receptor antagonists in the rat liver and cultured rat Kupffer cells. Hepatology 30:1206-14
Svetlov, S I; Howard, K M; Debuysere, M S et al. (1998) Secretory PAF-acetylhydrolase of the rat hepatobiliary system: characterization and partial purification. Am J Physiol 274:G891-900
Mustafa, S B; Olson, M S (1998) Expression of nitric-oxide synthase in rat Kupffer cells is regulated by cAMP. J Biol Chem 273:5073-80
Svetlov, S I; Liu, H; Chao, W et al. (1997) Regulation of platelet-activating factor (PAF) biosynthesis via coenzyme A-independent transacylase in the macrophage cell line IC-21 stimulated with lipopolysaccharide. Biochim Biophys Acta 1346:120-30
Howard, K M; Miller, J E; Miwa, M et al. (1997) Cell-specific regulation of expression of plasma-type platelet-activating factor acetylhydrolase in the liver. J Biol Chem 272:27543-8
Siafaka-Kapadai, A; Hanahan, D J; Javors, M A (1997) Oleic acid-induced Ca2+ mobilization in human platelets: is oleic acid an intracellular messenger? J Lipid Mediat Cell Signal 15:215-32

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