Innate differences and colostrum-induced alterations of jejunal mucosal proteins in piglets with intra-uterine growth restriction.
Br J Nutr
; 119(7): 734-747, 2018 04.
Article
em En
| MEDLINE
| ID: mdl-29569542
ABSTRACT
Mammalian neonates undergo rapid transitions from a sterile uterine environment with a continuous intravenous supply of nutrients to a microbe-rich environment with intermittent ingesting of colostrum/milk via the gut. Currently, little is known about the colostrum-induced alterations of intestinal mucosal proteins in piglets with intra-uterine growth restriction (IUGR). In this study, we sought to investigate the innate differences and effects of colostrum on alterations in small-intestinal proteomes of IUGR piglets. Two IUGR (approximately 0·9 kg) and two normal-birth weight (NBW; approximately 1·3 kg) piglets were obtained from each of six sows at birth. One half (n 12; 6 IUGR v. 6 NBW) of the selected newborn piglets were killed to obtain jejunum samples, and the other half (n 12; 6 IUGR v. 6 NBW) of the newborn piglets were allowed to suckle colostrum from their own mothers for 24 h before jejunum sample collection. On the basis of proteomic analysis, we identified thirty-one differentially expressed proteins in the jejunal mucosa between IUGR and normal neonates before or after colostrum consumption. The intestinal proteins altered by colostrum feeding play important roles in the following (1) increasing intestinal integrity, transport of nutrients, energy metabolism, protein synthesis, immune response and, therefore, cell proliferation; and (2) decreasing oxidative stress, and therefore cell apoptosis, in IUGR neonates. However, colostrum only partially ameliorated the inferior status of the jejunal mucosa in IUGR neonates. These findings provide the first evidence in intestinal protein alterations of IUGR neonates in response to colostrum ingestion, and thus render new insights into the mechanisms responsible for impaired growth in IUGR neonates and into new nutritional intervention strategies.
Palavras-chave
ACTB ß-actin; ALB albumin; ANXA4 annexin A4; ANXA5 annexin A5; BW body weight; CALM calmodulin; CALR calreticulin; CAT catalase; CPS1 carbamoyl-phosphate synthetase 1; D0 day 0; D1 day 1; EEF2 eukaryotic translation elongation factor 2; EIF5A eukaryotic translation initiation factor 5A-1; EIF6 eukaryotic translation initiation factor 6; FBP1 fructose 1; GRP78 glucose-regulated protein; HSPA1B heat shock 70 kDa protein 1B; IUGR intra-uterine growth restriction; LMNA lamin A/C; MFGE8 milk fat globule-EGF factor 8 protein; NBW normal-birth weight; PRDX1 peroxiredoxin 1; RPSA laminin receptor 1; SDHA succinate dehydrogenase complex subunit A; STRAP serine/threonine kinase receptor-associated protein; TF transferrin; VCL vinculin; 6-bisphosphatase; Colostrum; Intra-uterine growth restriction; Jejunum; Porcine neonates; Proteomics
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Doenças dos Suínos
/
Colostro
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Retardo do Crescimento Fetal
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Mucosa Intestinal
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Jejuno
Tipo de estudo:
Prognostic_studies
Limite:
Animals
/
Pregnancy
Idioma:
En
Revista:
Br J Nutr
Ano de publicação:
2018
Tipo de documento:
Article