Literature DB >> 6309795

Acetylglyceryl ether phosphorylcholine. A potent activator of hepatic phosphoinositide metabolism and glycogenolysis.

S D Shukla, D B Buxton, M S Olson, D J Hanahan.   

Abstract

Acetylglyceryl ether phosphorylcholine (AGEPC), or 1-O-Alkyl-2-acetyl-sn-glyceryl 3-phosphorylcholine, has been shown to have a dramatic influence on phosphoinositide metabolism in isolated rat hepatocytes and upon glycogenolysis in the intact perfused rat liver. Addition of 5 X 10(-10) M AGEPC to 32Pi-labeled rat hepatocytes resulted in up to a 30 to 40% decrease in the [32Pi]phosphatidylinositol 4,5-bisphosphate within 10 s. The 32P content of phosphatidylinositol 4-phosphate decreased approximately 25% within 60 s, while a 5 to 8% decrease in [32P]phosphatidylinositol was observed only after 2 to 5 min of incubation of hepatocytes with AGEPC. Infusion of AGEPC (2 X 10(-10) M) into perfused livers resulted in a 3-fold increase in the glucose output in the effluent perfusate within 2 min. Interestingly, when a 500-fold higher concentration, i.e. 1 X 10(-7) M, of 1-O-alkyl-sn-glyceryl 3-phosphorylcholine or the stereoisomer 3-O-alkyl-2-acetyl-sn-glyceryl 1-phosphorylcholine was infused, no increase in the hepatic glucose output was seen. These observations lead to the conclusion that AGEPC exerts a potent influence on the polyphosphoinositide metabolism and glycogenolysis in rat liver and establishes the liver as an ideal system in which to conduct a detailed inquiry into the biochemical mechanism(s) responsible for the biological action of this unusual phospholipid.

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Year:  1983        PMID: 6309795

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  26 in total

1.  Glycogenolytic and haemodynamic responses to heat-aggregated immunoglobulin G and prostaglandin E2 in the perfused rat liver.

Authors:  D B Buxton; R A Fisher; D L Briseno; D J Hanahan; M S Olson
Journal:  Biochem J       Date:  1987-04-15       Impact factor: 3.857

Review 2.  Non-parenchymal cells as mediators of physiological responses in liver.

Authors:  J G Altin; F L Bygrave
Journal:  Mol Cell Biochem       Date:  1988-09       Impact factor: 3.396

3.  PAF effects on transmembrane signaling pathways in rat Kupffer cells.

Authors:  C R Gandhi; M S Olson
Journal:  Lipids       Date:  1991-12       Impact factor: 1.880

Review 4.  Inositol phospholipid turnover in PAF transmembrane signalling.

Authors:  S D Shukla
Journal:  Lipids       Date:  1991-12       Impact factor: 1.880

5.  Conditioned media of Kupffer and endothelial liver cells influence protein phosphorylation in parenchymal liver cells. Involvement of prostaglandins.

Authors:  E Casteleijn; J Kuiper; H C Van Rooij; J F Koster; T J Van Berkel
Journal:  Biochem J       Date:  1988-06-01       Impact factor: 3.857

6.  Protein tyrosine phosphorylation and regulation of the receptor for platelet-activating factor in rat Kupffer cells. Effect of sodium vanadate.

Authors:  W Chao; H Liu; D J Hanahan; M S Olson
Journal:  Biochem J       Date:  1992-12-15       Impact factor: 3.857

7.  Stimulation of uric acid release from the perfused rat liver by platelet activating factor or potassium.

Authors:  C E Hill; M S Olson
Journal:  Biochem J       Date:  1987-10-01       Impact factor: 3.857

8.  Renal effects of platelet-activating factor in the rat.

Authors:  G Friedlander; E Pirotzky; C Amiel; J Benveniste
Journal:  Agents Actions       Date:  1987-10

9.  Location of platelet activating factor binding in rat liver.

Authors:  C E Hill; M Miwa; P J Sheridan; D J Hanahan; M S Olson
Journal:  Biochem J       Date:  1988-08-01       Impact factor: 3.857

10.  Human endothelial cells in culture produce platelet-activating factor (1-alkyl-2-acetyl-sn-glycero-3-phosphocholine) when stimulated with thrombin.

Authors:  S M Prescott; G A Zimmerman; T M McIntyre
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

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