Ml. Blank et al., MOLECULAR-SPECIES OF ETHANOLAMINE PLASMALOGENS AND TRANSACYLASE ACTIVITY IN RAT-TISSUES ARE ALTERED BY FISH-OIL DIETS, Biochimica et biophysica acta, L. Lipids and lipid metabolism, 1214(3), 1994, pp. 295-302
Effects of dietary fish oil ethyl esters and alkyldiacetylglycerols (a
n ether-linked lipid) on the distribution of subclasses of choline- an
d ethanolamine-glycerophospholipids as well as effects on highly unsat
urated molecular species of ethanolamine plasmalogens from brain, sple
en, kidney, lung, and testis of rats were examined. Supplementation of
ethyl ester concentrates of n - 3 fatty acids had no effect on the di
stribution of subclasses in any of the tissues. However, the supplemen
ts of 1-O-octadec-9'-enyl-2,3-diacetyl-sn-glycerol (diacetates of sela
chyl alcohol) caused significant increases in the alkylacylglyceraphos
phocholine and alkylacylglycerophosphoethanolamine subclasses from spl
een and lung and in the alkylacylglycerophosphoethanolamine subclass f
rom kidney. Dietary supplements of fish oil ethyl eaters reduced the a
rachidonate-containing species of ethanolamine plasmalogens whereas mo
lecular species having 20:5(n - 3), 22:6(n - 3), and/or 22:5(n - 3) ac
yl groups were increased in the spleen, lung, and kidneys, but not bra
in. In testicular tissue from rats fed the fish oil diets, the molecul
ar species of ethanolamine plasmalogens containing 22:5(n - 6) acyl gr
oups were reduced. An increase of ethanolamine plasmalogens with 18:1
alk-1-enyl moieties paired with highly unsaturated sn-2 acyl groups we
re found in the tissues of rats fed the fish oil plus selachyl alcohol
diacetate supplements. Rats on the diet containing fish oil ethyl est
ers had significantly lower [H-3]alkyllysoglycerophosphocholine CoA-in
dependent transacylase activity in spleen microsomes than controls. Th
is suggests that supplements of n - 3 fatty acids interferes with the
transacylation of arachidonate, an event that could seriously impair t
he release of arachidonate and lysophospholipids (e.g., lyso-PAF) that
are precursors of potent bioactive lipid derivatives.