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THE FABULOUS DESTINY OF FATTY ACIDS<br />

example to ameliorate dairy cow fertility (Santos et al., 2008; Silvestre et al., 2011;<br />

Thatcher et al., 2011).<br />

CHALLENGES WHEN FEEDING FATTY ACIDS TO DAIRY CATTLE<br />

BIOHYDROGENATION, ABSORPTION AND DISTRIBUTION OF FATTY ACIDS<br />

The dietary FA reflect the FA composition <strong>of</strong> pig <strong>and</strong> poultry products in a<br />

predictable way because they are absorbed unchanged before incorporation into the<br />

tissue lipids (Chesworth et al., 1998; Woods <strong>and</strong> Fearon, 2009). In contrast, increasing<br />

the amount <strong>of</strong> dietary UFA in the diet <strong>of</strong> ruminants is not linearly reflected in the body<br />

tissues as microorganisms in the rumen largely affect the composition <strong>of</strong> the FA (Doreau<br />

<strong>and</strong> Chilliard, 1997; Jenkins et al., 2008). The microorganisms are responsible for the<br />

isomerisation <strong>and</strong> hydrolysis <strong>of</strong> dietary lipids, <strong>and</strong> the conversion <strong>of</strong> UFA to various<br />

partially hydrogenated intermediates such as cis-9, trans-11 CLA or 18:1 trans-11, <strong>and</strong><br />

other fully saturated derivates such as 18:0 (Woods <strong>and</strong> Fearon, 2009). This process,<br />

also called ruminal biohydrogenation (Figure 3), causes the major FA exiting the rumen<br />

to be 18:0, although the main FA in most seed lipids <strong>and</strong> forages are 18:2n-6 <strong>and</strong> 18:3n-<br />

3 respectively (Palmquist <strong>and</strong> Jenkins, 1980). In general, rates <strong>of</strong> rumen<br />

biohydrogenation are faster with increasing unsaturation, showing hydrogenation rates<br />

<strong>of</strong> 18:2n-6 <strong>and</strong> 18:3n-3 up to 70-95% <strong>and</strong> 85-100% respectively (Lock et al., 2006).<br />

Biohydrogenation <strong>of</strong> 20:5n-3 <strong>and</strong> 22:6n-6 is still not well understood, but at present<br />

they are believed to be hydrogenated at the same extent as 18:2n-6 <strong>and</strong> 18:3n-3<br />

(Shingfield et al., 2010). Due to the extensive biohydrogenation <strong>of</strong> FA, ruminants seem to<br />

have developed very efficient pathways for capturing <strong>and</strong> maintaining essential FA<br />

within the body as functional deficiencies do not occur (Drackley, 2005).<br />

There is no significant absorption or hydrogenation <strong>of</strong> LCFA in the omasum or<br />

abomasums; the lipid material available for absorption in the small intestine is similar to<br />

that leaving the rumen (Moore <strong>and</strong> Christie, 1984). Approximately 80-90% <strong>of</strong> lipids are<br />

entering the small intestine as free FA attached to feed particles, bacteria <strong>and</strong><br />

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