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of CLA isomers in the umbilical cord plasma, colostrum, and milk, and subsequently
increased CLA concentrations in plasma, backfat, and longissimus dorsi of neonatal
and weanling piglets (Bee, 2000a,b; Peng et al. , 2010; Poulos et al. , 2004; Schmid et al. ,
2008). Interestingly, in the findings of Peng et al. (2010), both cis -9, trans -11-18:2 and
trans -10, cis -12-18:2 could be detected in colostrum and milk but only trans -10, cis -
12-18:2 could be detected in umbilical cord plasma, indicating that there might be some
differences in CLA transfer patterns between umbilical cord blood and milk.
16.4.4
Feeding strategy for conjugated linoleic acid
Numerous studies showed that supplementation of sow diets with CLA significantly
improves the immune status of sows and their offspring. However, the duration of dietary
CLA supplementation in sows may affect the extent of growth, immune components,
and metabolic and hormonal responses in lactating sows and their piglets (Corini et
al. , 2009). Peng et al. (2010) demonstrated that dietary CLA supplied during late
gestation and lactation altered the FA profiles of umbilical cord blood and milk and
led to a complex transfer pattern from the sow to the piglets. Therefore, many studies
were carried out using a CLA supplementation period starting in late pregnancy and
continuing throughout lactation (Bontempo et al. , 2004; Codero et al. , 2011; Krogh et al. ,
2012; Peng et al. , 2010). Whereas in some studies sows were fed diets supplemented with
CLA from mid-gestation through weaning (Patterson et al. , 2008; Poulos et al. , 2004),
in other studies sows were fed CLA throughout gestation and lactation (Bee, 2000a,b).
Corino et al. (2009) evaluated two different periods for feeding 0.5% dietary CLA,
namely, from 7 d before parturition to 7 d postpartum, or from 7 d before parturition
until weaning. They found that beneficial effects in terms of body weight at weaning and
immune components of piglets were greater with a supplementation from 7 d before
parturition until 7 d postpartum. Park et al. (2005) observed that feeding sows with CLA
from 15 d pre-mating to weaning led to lower weights of piglets at d 21 than when sows
were fed CLA from 74 d post-mating to weaning. However, Poulos et al. (2004) did not
find any difference in piglet growth when sows were fed CLA from either 40 d or 75 d of
gestation until weaning.
The 0.5% supplementation level of CLA was shown to have beneficial effects on
immunologic variables in lactating sows and piglets (Bontempo et al. , 2004), as well as on
piglet growth (Corino et al. , 2009). Greater supplementation levels, such as 1% (Codero
et al. , 2011), 1.3% (Krogh et al. , 2012), or 2% (Bee, 2000a,b; Patterson et al. , 2008),
also had many positive effects on sows or their offspring. Peng et al. (2010) reported
that concentrations of the CLA isomers in umbilical cord blood, plasma, backfat, and
longissimus dorsi of neonatal (2 d of age) and weanling (26 d of age) piglets increased
linearly when CLA supplementation went from 0.5% to 1.0%. However, Park et al. (2005)
found that piglet birth weights were lower with a high dietary level of CLA (2%) and a
longer feeding duration (from d 15 pre-mating to weaning).
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