Quick changes in milk fat composition from cows after transition from fresh grass to a silage diet
Introduction
There is nowadays much interest in adaptation of the fatty acid (FA) profile of milk fat due to consumer demands for dietary unsaturated fatty acids (UFA). UFA are favourable against coronary heart diseases (Williams, 2000). Some UFA, particularly vaccenic acid (C18:1, trans-11) (Banni et al., 2001, Turpeinen et al., 2002), omega-3 polyunsaturated fatty acids (PUFA) such as linolenic acid (C18:3) and conjugated linoleic acid (CLA), especially rumenic acid (C18:2 cis-9, trans-11) (Martin and Valeille, 2002) have shown additional positive health effects in experimental animals, such as prevention of mammary gland and skin tumours.
CLA is a term to describe a mixture of positional and geometrical isomers of linoleic acid (C18:2) with conjugated double bonds. The beneficial rumenic acid is quantitatively the most important CLA isomer in milk fat. Also vaccenic acid has been claimed to have anticarcinogenic properties, probably due to the in vivo conversion into rumenic acid (Corl et al., 2003, Turpeinen et al., 2002). Because rumenic acid and vaccenic acid are both n-7 trans fatty acids, which are naturally almost only present in milk and meat from ruminants, Ellen and Elgersma (2004) suggested to refer to them as n-7 fatty acids, or use their individual trivial names, in order to avoid confusion with other CLA-isomers or trans fatty acids in general, which are associated with negative health effects.
Reported effects on the body composition changes, notably a reduction in the fat to protein ratio, are due to the C18:2 trans-10, cis-12 (Park et al., 1999), but liver-fattening and liver-enlarging effects of this CLA isomer were reported in mice (Warren et al., 2003).
There are two pathways for the production of CLA in the dairy cow. Firstly, they are formed as intermediates through incomplete biohydrogenation of PUFA from the diet by anaerobic rumen micro organisms. This reaction is catalyzed by linoleic acid isomerase, produced by the ruminal bacterium Butyrivibrio fibrisolvens (Kepler et al., 1966). Thus, the factors that determine the amount of CLA that is available for absorption from the gastrointestinal tract are the dietary intake of C18:2 and C18:3 and rumen conditions that may affect the growth and activity of B. fibrisolvens (Dhiman et al., 1995, French et al., 2000). Secondly, CLA are formed in the intermediary metabolism by desaturation of monounsaturated fatty acids (MUFA) (Griinari et al., 2000), through endogenous synthesis in the mammary gland from vaccenic acid due to delta-9-desaturase activity (Baumgard et al., 2000). Vaccenic acid may thus serve as a precursor for CLA in the mammary gland (Salminen et al., 1998).
Animals grazing fresh grass have higher levels of CLA (Stanton et al., 1997, Kelly et al., 1998, Lawless et al., 1998, Dhiman et al., 1999) in their milk and meat than those consuming conserved forages. Pasture is a richer source of PUFA than silage (Harfoot and Hazlewood, 1997). Besides, Elgersma et al. (2003a) discovered that whereas in fresh grass 0.98 of the fat was present as esterified fatty acids (EFA), in grass silage a large proportion was present as free fatty acids (FFA). During the conservation process, PUFA in herbage that are precursors for the FA in milk may be lost. Dewhurst and King (1998) and Elgersma et al. (2003a) reported a decrease in FA content and in the proportion of α-linolenic acid in ensiled material compared to fresh grass. Therefore, the transition from summer feeding to winter feeding, i.e. from pasture to silage will decrease the intake of UFA. It is hypothesized that this will shift the ratio between the unsaturated and the saturated milk fat fraction in the direction of the saturated fraction, which implies that less CLA will be present in milk after transition.
Kelly et al. (1998) studied changes during transition from a winter diet to fresh grass, but information on the reverse process is lacking and data on the rate of change during transition are scarce. The objectives of this study were, therefore, to examine the effects of transition and the rate of changes in the profile of milk FA in individual cows during transition from fresh grass to a grass/maize silage diet.
Section snippets
Materials and methods
All procedures involving animals were approved by and proceeded under supervision of the appropriate authorities (Wageningen University ‘Dier Experimenten Commissie’).
Diet composition
The chemical compositions of the feeds in the ration are shown in Table 2. Table 3 shows the fat content and FA composition of the feeds of which the diet was composed. Grass silage had the highest fat content (13.1 g/kg) and the highest amount of FFA (9.2 g/kg). A substantial part of the FA was present as FFA in the silages, but in the concentrate only EFA were present. The FA composition differed among feeds. Concentrate and maize silage contained mostly C18:2 and grass silage mostly C18:3. The
Changes in diet composition, intake, milk production and milk fatty acid composition related to diet
As levels of dry matter intake and MP did not change, milk FA changes can be related to dietary changes. After transition, the average milk fat content increased and the milk fatty acid composition altered within two days. In contrast to Kelly et al. (1998), the cows generally responded similarly to the transition. The range in CLA concentrations among individual cows was larger than in their experiments. Concentrations in milk of cows on grazed grass were at a higher level than reported by
Conclusions
After transition of cows from fresh grass to a silage-based diet, the average milk fat content increased within two weeks. Although MP was maintained after transition, the milk FA composition altered dramatically within a few days. Both trials gave consistent results. The UFA content of milk fat decreased, while the SFA and SMCFA contents of milk fat increased within days, which is undesirable from a consumer health viewpoint. The contents of the beneficial n-7 FA rumenic acid and vaccenic acid
Acknowledgements
We thank the Wageningen University staff of the Ossekampen, in particular Mr. L. Bijl, for technical assistance. Mr. B. Tas and Mr. H. Smit assisted in sample handling. H. van der Horst acknowledges financial support of the Grassland Science Foundation (SGW). The work was partly funded by the Commodity Board for Dairy Products in Zoetermeer, The Netherlands.
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