Five sheep with rumen and abomasal cannulae were offered three diets sequen
tially in the order: control (C) pellets (lucerne hay-oat grain: 60/40, w/w
), control plus unprotected tuna oil (UTO pellets), and control plus tuna o
il protected (casein-formaldehyde matrix) against ruminal biohydrogenation
(PTO pellets). In supplemented diets, tuna oil constituted 3% (w/w) of tota
l dry matter (DM), and each supplement was fed for 12 days, with 9 days all
owed between the two fish oil feeding periods to minimise carry-over effect
s. Daily DM intake was 785 +/- 38 g/head during the control period. It was
significantly reduced by UTO feeding (6.2%, P < 0.05) but not PTO feeding.
The level of EPA in the abomasum during PTO feeding was double that measure
d during UTO feeding (1.30 versus 0.61% of FA, P < 0.05). The level of DHA
in the abomasum did not significantly differ between UTO and PTO feeding pe
riods. Both tuna oil supplements significantly increased the levels of 18:1
trans and that of a fatty acid derivative identified as 10-hydroxystearic
acid(10-HSA) in both the rumen and abomsum. Tuna oil supplementation also a
ltered the fatty acid composition of plasma lipid fractions and 10-HSA was
solely incorporated into plasma free fatty acids. This study indicates that
substantial protection of tuna oil against ruminal hydrogenation inhibited
reduced feed intake, but increased the proportion of 18:1 trans isomer and
fatty acids derivatives (10-HSA), which indicate interference with metabol
ism in the rumen. (C) 2001 Published by Elsevier Science B.V.