Jh. Spalinger et al., UPTAKE AND METABOLISM OF STRUCTURED TRIGLYCERIDE BY CACO-2 CELLS - REVERSAL OF ESSENTIAL FATTY-ACID DEFICIENCY, American journal of physiology: Gastrointestinal and liver physiology, 38(4), 1998, pp. 652-659
Structured lipids have been proposed as efficient vehicles for the sup
plementation of essential fatty acids (EFA) to patients with malabsorp
tion. We investigated how a novel structured triglyceride (STG), conta
ining purely octanoic acid in the sn-1/sn-3 and [C-14]linoleic acid in
the sn-2 positions, was incorporated into different lipid classes in
Caco-2 cells. We also evaluated the contribution of gastric Lipase in
the uptake and metabolism of [C-14]linoleic acid from the STG. We furt
hermore determined the potential of the STG to correct EFA deficiency
induced in Caco-2 cells. The absorption of STG by Caco-2 cells was sig
nificantly greater compared with that of triolein. The addition of hum
an gastric lipase significantly enhanced cellular uptake of the labele
d substrate, reflecting the stereoselectivity of gastric lipase to hyd
rolyze medium chain FA. Analysis of the intracellular lipids synthesiz
ed revealed a predominance of phospholipids-monoglycerides. Most of th
e radioactivity in the lipoproteins isolated from Caco-2 cells was rec
overed in TG-rich lipoproteins (45%) and to a lesser extent in the hig
h-density lipoprotein (36%) and low-density Lipoprotein (17%) fraction
s. The administration of STG to Caco-2 cells rendered EFA deficient pr
oduced a marked increase of the cellular level of linoleic and arachid
onic acids. This resulted in a lower ratio of 20:3(n-9) to 20:4(n-6),
reflecting the correction of EFA deficiency in Caco-2 cells. Our data
demonstrate that STG, in the presence of gastric Lipase, have benefici
al effects on lipid incorporation, lipoprotein production, and EFA sta
tus, utilizing Caco-2 cells as a model of EFA deficiency.