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Journal of Lipid Research, Vol 25, 121-128, Copyright © 1984 by Lipid Research, Inc.
S Eisenberg, Y Oschry and J Zimmerman
The intravascular metabolism of the cholesteryl ester moiety of rat plasma
LDL, HDL1, and HDL2 was determined in intact male rats. Biosynthetically
labeled lipoproteins were prepared by zonal ultracentrifugation from the
plasma of rats injected with [3H]cholesterol. The lipoproteins were
concentrated by vacuum ultrafiltration as other procedures were found to
alter the biological properties of the lipoproteins. After injection of
labeled LDL, [3H]cholesteryl esters remained with the injected lipoprotein
and decayed from plasma with a t1/2 of 7-8 hours. [3H]Cholesteryl esters in
HDL1 behaved similarly and decayed with a t1/2 of 10.5 hours. With HDL2,
however, a different metabolic pattern was observed with intraplasma
conversion of some [3H]cholesteryl ester HDL2 particles to HDL1. Since such
conversion of HDL2 to HDL1 was not observed after in vitro incubations of
rat plasma, this process seems to depend on metabolic events that occur in
vivo. [3H]Cholesteryl esters disappeared from HDL2 with a t1/2 of 6-7
hours, while the esters that were transferred to HDL1 decayed with a t1/2
of 10-11 hours, similar to labeled cholesteryl esters injected with HDL1.
The study demonstrated that the high apoE content of rat plasma HDL1 is not
associated with rapid catabolism of the lipoprotein and that a major source
of HDL1 in the rat is the intraplasma conversion of HDL2 particles to HDL1.
ARTICLES
Intravascular metabolism of the cholesteryl ester moiety of rat plasma lipoproteins
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