DNA polymorphism of the porcine leukemia inhibitory factory (LIF) was investigated and used to study the effects on litter size in Large White pigs. A total of 2,167 litter records from 420 sows genotyped at two SNP loci (LIF1 and LIF2) within LIF gene were analyzed to determine whether LIF influenced total number born (TNB) and number born alive (NBA). The results indicated that B allele at LIF1 locus and A allele at LIF2 locus seem to have advantageous effects on litter size. However, the combined analyzed results demonstrated that genotype AAAA, ABBB, and BBBB are better than genotype AAAB, AABB, and ABAB for TNB and NBA in either third to eighth parity or all parities. In all parities, the sows with AAAA genotype had an advantage of 1.76 piglets (P < 0.001) for TNB and 1.44 piglets (P < 0.01) for NBA per litter over the AAAB sows, respectively. The results in this study demonstrated that LIF gene was significantly associated with litter size in pigs.
The objective of this study was to determine whether peroxisome proliferator-activated receptor γ (PPARγ) is involved in the regulation of weaning to estrus of primiparous sows. Twelve sows composed of 6 groups of 2 full-sibs in a similar age (325.2 d), body weight (BW; 152.4 kg) and backfat thickness (BFT; 27.0 mm) at start of lactation, were allocated to accept 31 MJ (restricted group, R-group) or 53 MJ (control group, C-group) DE/d treatment, respectively. The experimental results indicated that the low energy intake resulted in excessive losses of BW and BFT during lactation in R-group sows, which may be related to decrease of serum 15deoxy-∆ 12,14 -prostaglandin J 2 (15d-PGJ 2 ), a ligand of PPARγ. The obvious peak and the frequency of LH, FSH and estradiol (E 2 ) were only observed in C-group sows. Except for E 2 at d 1 and 2, serum FSH, LH and E 2 concentrations in R-group were lower than those in C-group sows after weaning. However, the serum progesterone (P 4 ) level in R-group sows was always more than that in C-group. The expression abundances of PPARγ and GnRH receptor (GnRH-R) in pituitary, FSH receptor (FSH-R), LH receptor (LH-R), estrogen receptor (ES-R) and aromatase in ovary of anestrous sows were lower than those of estrous sows. Neither the BFT nor the BW was associated with the mRNA abundance of PPARγ in hypothalamus during lactation. Expressions of PPARγ in pituitary and ovary were affected evidently by the BFT changes and only by the loss of BW of sows during and after lactation. Furthermore, PPARγ mRNA level in ovary was significantly related to the expression abundances of GnRH-R, FSH-R, ES-R and aromatase, and GnRH-R was obviously associated with PPARγ expression in pituitary. However, PPARγ expression in hypothalamus likely has no effects on these genes expression and no obvious difference for all sows. Not serum E 2 or P 4 alone but the ratios of E 2 to P 4 and 15d-PGJ 2 to P 4 , and serum FSH and LH were evidently related to PPARγ expression in pituitary and ovary. It is concluded that PPARγ is associated with body conditions, reproduction hormones and their receptor expression, which affected the functions of pituitary and ovary and ultimately the estrus after weaning of primiparous sows.
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