The major trans isomers of alpha-linolenic acid (9c, 12c, 15t-, 9t 12c, 15c
-18:3 and 9t, 12c, 15t-18:3) are found in refined and frying oils, and ore
then ingested by humans. Among these isomers, it has been shown that 9c, 12
c, 15t-18:3 isomer can be desaturated and elongated into a Delta 17-trans i
somer of eicosapentaenoic acid (5c, 8c, 11c, 14c, 17t-20:5 or 17t-20:5). It
is present in tissues of rats fed heated oils. It is also present in human
platelet lipids, suggesting that similar routes could exist in humans.
Previous studies on human platelets showed that the 17t-20:5 can alter aggr
egation as compared to its cis homologue, eicosapentaenoic acid, when it is
added by an exogenous route or incorporated into platelet lipids. Moreover
, it may compete with arachidonic acid metabolism.
A recent study was carried out on rat platelets triggered with arachidonic
acid. This study confirmed the antiaggregatory effect of 17t-20:5 and showe
d that the fatty acids containing a trans double bond at the Delta 11 posit
ion (11t- and 11t, 17t-20:5) were more antiaggregant than EPA. Furthermore,
in opposition to EPA, 17t-20:5 was also able to induce platelet aggregatio
n. It was metabolised into three compounds, among which two were formed thr
ough the cyclooxygenase pathway and one through the 12-lipoxygenase pathway
.
Platelet aggregation was studied in human involved in an European contract.
In this study, a randomised double blind dietary intervention trial was ca
rried out with healthy mole volunteers (n = 88) from three European centres
, Clermont-Ferrand (France, n = 31), Edinburgh (Scotland, n = 26) and Maast
richt (Netherlands, n = 31). After 6 weeks of a diet without food containin
g all trans fatty acid, subjects either continued for 6 week with a low tra
ns diet ora diet in which trans cx-linolenic acid provided 0.6% of energy.
Platelet aggregation was measured three times during the dietary interventi
on (0, 6 et 12 weeks).
As expected, this study showed that 15t-18:3 was converted into 17t-20:5 by
humans and the 17t-20:5 was the only EPA isomer incorporated in platelet p
hospholipids. But this incorporation was not sufficient to alter platelet a
ctivity and metabolism of arachidonic acid into thromboxane A(2). In conclu
sion, a 6 week-consumption of 0.6% of total energy as trans isomers of alph
a-linolenic acid did not modify the activity of human platelet, when aggreg
ation was induced by collagen or by a thromboxane A(2) analogue.