6 research outputs found

    Hindgut fermentation in pigs induced by diets with different sources of starch

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    A proportion of dietary starch reaches the hindgut, being fermented there. The characteristics of in vitro caecal fermentation and microbial community in pigs given different sources of starch were studied. Twenty-four Duroc × (Landrace × Large White) gilts given diets based on barley (B), broken rice (R), maize (M) or peas (P) (n=6) for five weeks were slaughtered with 93.6 ± 6.41 kg. No differences (p>0.10) were recorded in caecal pH, total short chain fatty acid (SCFA) and total bacterial concentration, nor in in vitro gas production from caecal contents, indicating the lack of a quantitative dietary effect on caecal environment. This could be partly due to the length of fasting time before slaughter (around 10 h). Molar SCFA proportions did not differ among diets; however, relative proportion of Lactobacillus sobrius/amylovorus as the species-type in starch digestion in hindgut of pigs, was highest with P diet (p = 0.010), and gas production from potato starch as substrate with P diet was highest at 2 h incubation (p = 0.012), and higher than B and R diets at 4 (p = 0.055) and 6 (p = 0.10) h incubation. Caecal bacterial biodiversity was higher for M and R diets than for P and B diets (Shannon index, p = 0.003). Sources of resistant or slowly digestible starch such as peas promote a microbial community with a different profile and higher capacity to ferment the starch arriving to the organ than other sources which are mostly digested in the small gut

    Long term vitamin A restriction improves meat quality parameters and modifies gene expression in Iberian pigs1

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    Vitamin A is a key regulator of gene expression, influencing adipogenesis and lipid metabolism in animal tissues. This experiment was conducted to assess the effect of dietary vitamin A level and administration time on productive traits, intramuscular fat (IMF) content in ham muscles, tissue fatty acid composition, and expression of a panel of adipogenic and lipogenic candidate genes in Iberian pigs. Sixty piglets of 16.3 kg (SD = 2.5 kg) live weight (LW) were either fed a vitamin A–enriched diet (10,000 IU vitamin A/kg; CONTROL, n = 20) or a diet without supplemented vitamin A, applied from 16.3 kg (SD = 2.5 kg; early restriction group, ER, n = 20) or from an average weight of 35.8 kg (SD = 3.1 kg; late restriction group, LR, n = 20). Two slaughters were performed when pigs reached the averaged weights of 101.4 (SD = 4.1 kg) and 157.9 kg LW (SD = 7 kg) and samples from liver, heart, and backfat were obtained in both sacrifice times. In addition, ham subcutaneous fat and Semimembranosus (SM) and Biceps Femoris (BF) muscles were sampled at the last sacrifice. Dietary vitamin A level produced no effect on carcass traits in any of the harvests, while a small effect was observed on fatty acid composition in backfat at 101.4 kg LW. However, at 157.9 kg LW, the ER and LR groups showed higher MUFA content and lower SFA content in backfat, ham fat, and IMF (P < 0.01). In IMF, a decrease in n-6/n-3 PUFA ratio was observed in the restricted groups (P < 0.005). Intramuscular fat content in SM muscle was greater (P < 0.05) in the ER group than in the CONTROL and LR groups, while no difference was detected in BF muscle. Little effect of dietary vitamin A was observed in liver. Regarding changes in gene expression, ACSL4, CEBPB, and IGF1 genes were upregulated (P < 0.0001, P < 0.0001, and P < 0.05, respectively) in the ER group in hepatic tissue, whereas CRABPII and SCD genes were upregulated (P < 0.05) in the same group in adipose tissue. On the other hand, RXRG was downregulated (P < 0.05) in the ER group in adipose tissue. Results found in this experiment show that long-term restriction of dietary vitamin A has a positive effect on nutritional and sensorial parameters of ham meat. Moreover, gene expression results were consistent with the vitamin A transcriptional regulation of adipogenesis and lipogenesis and with the changes observed in meat and fat composition. © 2015 American Society of Animal Science. All rights reserved.Peer reviewe
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