A soluble substance demonstrated to be released from leukocytes which caused platelet aggreg. (1971), which was confirmed & named PAF;
Also at this time an antiHT polar renal lipid (APRL) produced by interstitial cells of renal medulla was described, & this was concluded to be identical to PAF in 1979 & was then also synthesised & shown to be AGEPC - a phospholipid.
PAF actually represents a family of phospholipids & like the eicosanoids including prostaglandins are not stored in cells but synthesised in response to stimulation.
Biosynthesis:
Precursor is 1-O-alkyl-2-acyl-glycerophosphocholine - a lipid found in high [] in membranes of many cells;
1st step: Plipase A2 converts it to lyso-PAF & a FFA (usually arachid.acid)
2nd rate-limiting step:
lyso-PAF converted to PAF:
by acetyl-coA, catalysed by lyso-PAF acetyltransferase;
Both steps are regulated by Ca availability and stimulated by:
Usually synthesis → release from cell & act on G-protein-coupled receptors but in endothelial cells, it acts i/cellularly;
Inactivation of PAF:
Plasma & cytosolic PAF acetylhydrolase forms lyso-PAF which is then converted back to the PAF precursor by an acyltransferase which is inhibited by Ca;
Pharmacology of PAF:
CVS:
A potent vasodil. but high [] may → decr. flow due to plat.effect;