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From the Division of Lipoprotein Metabolism and Pathophysiology, Department of Physiology, Louisiana State University Medical Center, New Orleans.
Correspondence to Laurence Wong, Division of Lipoprotein Metabolism and Pathophysiology, Department of Physiology, Louisiana State University Medical Center, New Orleans, LA 70112.
Abstract We report the lipid composition of dog plasma and
peripheral lymph lipoproteins as separated into pre-ß,
, and pre-
fractions by agarose gel electrophoresis. Plasma
lipoproteins with
mobility have a composition different from that
of plasma lipoproteins with pre-
mobility, having 9% versus 11%
free cholesterol, 21% versus 17% cholesterol
ester, 1% versus 16% triacylglycerol, and 69%
versus 56% phospholipid. On the other hand, lymph
and pre-
lipoproteins have compositions that are quite similar (9% versus 7%
free cholesterol, 17% versus 17% cholesterol
ester, 2% versus 4% triacylglycerol, and 71%
versus 71% phospholipid). The lipid compositions of plasma and lymph
lipoproteins are quite similar (9% versus 9% free
cholesterol, 21% versus 17% cholesterol
ester, 1% versus 2% triacylglycerol, and 70%
versus 72% phospholipid). The lipid compositions of plasma and lymph
pre-
lipoproteins are different (11% versus 7% free
cholesterol, 17% versus 17% cholesterol
ester, 16% versus 4% triacylglycerol, and 56%
versus 71% phospholipid). Peripheral lymph lipoproteins
with pre-ß mobility contained 15% cholesterol, 13%
cholesterol ester, 10%
triacylglycerol, and 61% phospholipid. Compared
with plasma, peripheral lymph lipoproteins are free
cholesterolenriched in all fractions. Calculated
stoichiometric ratios of lipid to apoA-I indicate that pre-ß
lipoproteins contain one molecule of apoA-I per particle,
lipoproteins have two molecules of apoA-I per particle, and pre-
lipoproteins have four molecules of apoA-I per particle.
Key Words: high density lipoproteins phospholipids cholesterol cholesterol ester triacylglycerol
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