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Great Lakes Dairy Sheep Symposium - the Department of Animal ...

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CLA. Examination <strong>of</strong> physiological factors has established that milk fat content <strong>of</strong> cis-9, trans-<br />

11 CLA has little or no relation to milk or milk fat yield, parity, stage <strong>of</strong> lactation or breed (Lock<br />

and Bauman, 2004). This variation must <strong>the</strong>refore, in large part, be related to individual<br />

differences in rumen output <strong>of</strong> vaccenic acid and to a lesser extent cis-9, trans-11 CLA, and to<br />

<strong>the</strong> amount and activity <strong>of</strong> Δ 9 -desaturase. Undoubtedly, <strong>the</strong> variation in Δ 9 -desaturase among<br />

individuals has a genetic basis, and <strong>the</strong>re is currently interest in understanding <strong>the</strong> genetic<br />

variation and heritability <strong>of</strong> this enzyme. Increasing <strong>the</strong> activity <strong>of</strong> Δ 9 -desaturase via selection<br />

and/or nutritional manipulation <strong>of</strong>fer fur<strong>the</strong>r potential to enhance <strong>the</strong> level <strong>of</strong> cis-9, trans-11<br />

CLA in milk through increasing endogenous syn<strong>the</strong>sis (Figure 3). Increasing Δ 9 -desaturase<br />

activity would not only impact on <strong>the</strong> level <strong>of</strong> cis-9, trans-11 CLA in milk fat, but would also<br />

increase o<strong>the</strong>r unsaturated fatty acids that are products <strong>of</strong> this enzyme. Finally, <strong>the</strong> final<br />

concentration <strong>of</strong> cis-9, trans-11 CLA in dairy products is, in large part, related to <strong>the</strong> cis-9, trans-<br />

11 CLA concentration in <strong>the</strong> raw milk fat and <strong>the</strong> fat content <strong>of</strong> <strong>the</strong> final product. Any changes<br />

in <strong>the</strong> cis-9, trans-11 CLA content related to processing or to storage <strong>of</strong> dairy products are<br />

minimal when compared to <strong>the</strong> variations associated with diet formulations and differences<br />

among individual animals.<br />

We have used such feeding regimes and taken advantage <strong>of</strong> individual animal variation to<br />

produce cis-9, trans-11 CLA-enriched butter for use in biomedical studies with animal models. In<br />

a series <strong>of</strong> studies, we have shown that dietary consumption <strong>of</strong> cis-9, trans-11 CLA-enriched<br />

butter is effective in reducing <strong>the</strong> progression and incidence <strong>of</strong> tumors in a rat-model <strong>of</strong><br />

mammary cancer. These results are among <strong>the</strong> first to demonstrate that a naturally produced<br />

anticarcinogen, consumed as a component <strong>of</strong> a natural food, is effective in reducing cancer.<br />

Fur<strong>the</strong>rmore, vaccenic acid present in milk fat is also anticarcinogenic via its conversion to cis-9,<br />

trans-11 CLA by our own Δ 9 -desaturase enzyme system. Recently, we have shown that naturallyderived<br />

cis-9, trans-11 CLA also has potent antia<strong>the</strong>rogenic properties. See <strong>the</strong> review by Bauman<br />

et al. (2005a) for a detailed discussion <strong>of</strong> <strong>the</strong> biological effects <strong>of</strong> cis-9, trans-11 CLA and vaccenic<br />

acid.<br />

The increased interest in <strong>the</strong> effect <strong>of</strong> bioactive fatty acids in milk fat has led to a number <strong>of</strong><br />

recent studies reporting <strong>the</strong> effects <strong>of</strong> different diets on <strong>the</strong> fatty acid composition <strong>of</strong> sheep milk. An<br />

example <strong>of</strong> typical sheep milk fatty acid pr<strong>of</strong>ile is shown in Table 3 and is taken from our study<br />

reported earlier when ewes received <strong>the</strong> unsupplemented (Control) diet. In general, <strong>the</strong><br />

unsupplemented ewes had a milk fat content and fatty acid pr<strong>of</strong>ile similar to o<strong>the</strong>r studies with<br />

lactating sheep (Rotunno et al., 1998; Sevi et al., 2002). The content <strong>of</strong> cis-9, trans-11 in ewes<br />

fed <strong>the</strong> control diet was however, lower than that reported in a survey <strong>of</strong> ewes when grazing<br />

grass (Nudda et al., 2005), but comparable to values when a dried complete diet was fed (Luna et<br />

al., 2005). A recent review examined <strong>the</strong> effect <strong>of</strong> forage species and stage <strong>of</strong> growth on <strong>the</strong> cis-<br />

9, trans-11 CLA content <strong>of</strong> sheep milk fat under Mediterranean conditions (Cabiddu et al.,<br />

2005). As for dairy cows, feeding fresh lush pasture results in <strong>the</strong> highest cis-9, trans-11 CLA<br />

content <strong>of</strong> milk fat. Similarly, seasonal changes in <strong>the</strong> cis-9, trans-11 CLA content <strong>of</strong> sheep milk<br />

have been reported which were related to pasture quality and availability (Figure 6; Nudda et al.,<br />

2005). Finally, it has also recently been reported that <strong>the</strong> fatty acid composition <strong>of</strong> dairy<br />

products (ripened cheeses and ricotta) produced from CLA-enriched milk were dependent on <strong>the</strong><br />

fatty acid composition <strong>of</strong> <strong>the</strong> starting raw milk, with manufacturing, ripening and storage having<br />

little or no effect on <strong>the</strong> cis-9, trans-11 CLA content <strong>of</strong> <strong>the</strong> final product (Addis et al., 2005;<br />

78

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