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Journal of Lipid Research, Vol 36, 535-543, Copyright © 1995 by Lipid Research, Inc.
A Gedde-Dahl, T Ranheim, CA Drevon, S Skrede, RK Berge and AC Rustan
The effects of the hypolipidemic fatty acid analogue tetradecylthioacetic
acid (TTA) on synthesis and secretion of lipoproteins in CaCo-2 cells were
studied. Radiolabeled tetradecylthioacetic acid was absorbed and
metabolized as efficiently as oleic acid, although a discrepancy in the
metabolic fate was evident. Whereas tetradecylthioacetic acid was
incorporated into cell- associated triacylglycerol to the same extent as
normal fatty acids (e.g., oleic acid and palmitic acid), the amount of
triacylglycerol secreted from cells incubated with tetradecylthioacetic
acid was 8 to 10 times lower than the amount secreted from cells incubated
with palmitic acid and oleic acid, respectively. On the other hand, there
was an enhanced incorporation of tetradecylthioacetic acid into cell-
associated and secreted phospholipids. Despite incorporation of
tetradecylthioacetic acid into cellular triacylglycerol, unlike oleic acid,
tetradecylthioacetic acid did not stimulate production of
triacylglycerol-rich particles. Ultracentrifugation of basolateral media
from cells incubated with tetradecylthioacetic acid revealed low amounts of
triacylglycerol in the triacylglycerol-rich fraction (p < 1.006 g/ml),
suggesting secretion of lipoproteins with a higher density than
chylomicrons. However, the present study shows that the stimulated
triacylglycerol secretion caused by oleic acid was inhibited in the
presence of TTA. The decreased rate of triacylglycerol secretion from these
cells was not accompanied by a stimulation of fatty acid oxidation. Based
on these findings, we therefore suggest that tetradecylthioacetic acid
mainly affects secretion of lipoproteins in CaCo-2 cells.
ARTICLES
Tetradecylthioacetic acid (a 3-thia fatty acid) decreases triacylglycerol secretion in CaCo-2 cells
Department of Pharmacology, University of Oslo, Norway.
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