The addition of long-chain polyunsaturated fatty acids (LCP: C20, and
C22) to infant formula may permit fatty acid accretion rates similar t
o breast-fed infants, and may have long-term outcome benefits, such as
improved visual acuity and cognitive development. Although fish oil m
ay provide a source of n-3 LCP, sources of n-6 LCP have been more diff
icult to identify. The present study evaluates the effects of n-3 and
n-6 LCP derived from single-cell oils on liver, plasma, and brain fatt
y acid levels in a neonatal animal model. Newborn rat pups were suckle
d for 14 d by dams receiving diets containing n-3 LCP alone or combina
tions of n-3 LCP and increasing doses of linoleic acid (18:2n-6) or ar
achidonic acid (20:4n-6). Dietary groups received 2% n-3 LCP and 1, 2,
or 5% of either 18:2n-6 or 20:4n-6. The 20:4n-6 source also contained
modest levels of 18:2n-6. At the termination of the study, liver, pla
sma, and brain were obtained from the rat pups and the phospholipid fa
tty acid profiles determined. The results indicate complex interaction
s of n-3 and n-6 fatty acids. Groups receiving dietary 20:4n-6 in corp
orated higher levels of n-6 LCP into tissues than did the groups recei
ving 18:2n-6. The brain was relatively resistant to changes in fatty a
cid composition compared with the liver and plasma. As expected, tissu
e n-3 LCP levels were reciprocally related to n-6 levels. The present
results document that single-cell LCP oils are bioavailable in a neona
tal animal model. The use of 20:4n-6 is a more effective means of supp
orting n-6 status than the use of 18:2n-6. These results may have impl
ications for the addition of LCP to infant formula.