Since the original investigations of Gage & Fish (1 924) on the dynamics of large chylomicron particles during postprandial lipaemia, measurements of triacylglycerol-rich lipoproteins (TRL) after ingestion of fat-rich meals have been utilized to provide information about the metabolism of these intestinal lipoprotein particles in vivo. There are many similarities, however, between the metabolism of chylomicrons and hepatogenous VLDL (Havel, 1989), so that observations in the postprandial state may provide generally applicable information about the regulation of TRL metabolism. Recently, it has become possible to distinguish the dynamics of chylomicron and VLDL particles separately by analysing the fluctuations of the concentrations of the two forms of apolipoprotein (apo) B with which they are associated B-48 and B-100 respectively (Havel, 1994).The overall pathway of absorption of dietary lipids has long been known and the rapid clearance and metabolism of chylomicron triacylglycerols was appreciated early in this century. The modern era of research in this area, however, had to await the development of methods to separate and characterize plasma lipoproteins (Gofman et al. 1949; Havel et af. 1955) and was greatly stimulated by the discovery of lipoprotein lipase (EC 3.1.1.34; Korn, 1955) and the demonstration that genetic deficiency of this enzyme dramatically reduces the rate of clearance of dietary fat from the blood (Havel & Gordon, 1960). Related physiological studies showed that chylomicron triacylglycerols are rapidly hydrolysed and that their products, free fatty acids (FFA), are concomitantly released and transported in the blood bound to albumin (Havel & Fredrickson, 1956).
DELINEATION OF THE CHYLOMICRON PATHWAYEarly studies of postprandial lipaemia in normal adults showed that all the major lipids of TRL rise and fall together with triacylglycerols (Havel, 1957). These studies also showed that HDL-lipids are affected by fat ingestion, and that HDL-phospholipid concentrations in particular are substantially increased (Havel, 1957; Havel et af. 19736). Subsequent studies in animals showed that the metabolism of the second major core component of chylomicrons, cholesteryl esters, differs dramatically from that of triacylglycerols, and led to a two-step model of chylomicron metabolism. In hepatectomized dogs, clearance from the blood of cholesteryl esters of chylomicrons but not triacylglycerols, was substantially impeded (Nestel et al. 1963). Furthermore, the majority of triacylglycerolfatty acids from chylomicrons were taken up by extrahepatic tissues, whereas component cholesteryl esters were removed almost quantitatively by the liver (Bergman et al. 1971). The liver also took up 10-20 % of intact chylomicron triacylglycerols in dogs and sheep as well as about one-fifth of the chylomicron triacy lglycerol-fatty acids released in extrahepatic tissues by the action of lipoprotein lipase on chylomicron triacylglycerols (Bergman et al. 1971). These and other studies in several mammalian species (Redgrav...