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CHAPTER 2<br />

predominant lipoprotein in bovine FF. The difference in ability to transverse the bloodfollicle<br />

barrier <strong>and</strong> the different FA pr<strong>of</strong>iles <strong>of</strong> the lipoproteins will have a pr<strong>of</strong>ound<br />

effect on the FA composition <strong>of</strong> the FF when supplementing PUFA to dairy cows.<br />

Furthermore, it has been suggested that the ovary is capable <strong>of</strong> buffering oocytes against<br />

fluctuations in the n-6 <strong>and</strong> n-3 content <strong>of</strong> plasma (Fouladi-Nashta et al., 2009). However,<br />

data on transfer <strong>of</strong> n-6 <strong>and</strong> n-3 FA to the follicle, especially the very LCFA such as 20:4n-<br />

6 or 22:6n-3 is lacking. As many mechanism by which FA affect reproduction in dairy<br />

cows (see below) rely on an efficient transfer through the blood-follicle barrier, this<br />

necessitates further research.<br />

SUPPLEMENTATION OR MOBILISATION DURING NEGATIVE ENERGY BALANCE<br />

Feeding supplemental FA to lactating dairy cows decreases the de novo synthesis<br />

<strong>of</strong> milk FA due to the incorporation <strong>of</strong> added dietary FA into the milk. This subsequently<br />

reduces the requirement for acetate, BHBA <strong>and</strong> NADPH, the latter being produced<br />

through oxidation <strong>of</strong> glucose. Secondly, dietary FA can induce insulin resistance in<br />

muscle <strong>and</strong> adipose tissue, which decreases peripheral glucose use (Chilliard <strong>and</strong> Ottou,<br />

1995; Gaynor et al., 1996; Pires et al., 2008). The spared glucose is partitioned towards<br />

increased lactose synthesis, hence increasing milk yield (Wu <strong>and</strong> Huber, 1994; Hammon<br />

et al., 2008). Although highly variable, the milk yield response to supplemental FA in<br />

TMR diets generally is curvilinear, increasing until approximately 9% <strong>of</strong> ether extract<br />

(EE) in the total diet (Wu <strong>and</strong> Huber, 1994) or 3% <strong>of</strong> added fat (Drackley, 1999),<br />

thereafter decreasing due to the concomitant decrease in DMI <strong>and</strong> fiber digestibility<br />

(Palmquist <strong>and</strong> Jenkins, 1980; Coppock <strong>and</strong> Wilks, 1991; Allen, 2000). Moreover, cows<br />

seem to respond production wise best to additional fat at the time they reach positive<br />

energy balance (Grummer, 1995). Consequently, the effect <strong>of</strong> an increased milk yield<br />

seems to be limited within the first 5 weeks post partum (Schingoethe <strong>and</strong> Casper, 1991;<br />

Chilliard, 1993; Grummer et al., 1995). The response lag <strong>of</strong> a few weeks, documented for<br />

both cows <strong>and</strong> heifers, is another drawback when supplementing FA to dairy cows in<br />

early lactation (Grummer, 1995). In summary, these findings illustrate the limited<br />

effectiveness <strong>of</strong> post partum dietary FA in order to ameliorate the NEBAL <strong>and</strong><br />

consequently have eliminated FA from most early lactation rations for dairy cows as<br />

they may imbalance the relative proportions <strong>of</strong> glucogenic <strong>and</strong> ketogenic metabolites<br />

30

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