INRA, UMR 1079, SENAH, F-35590 Saint-Gilles, France.
J Nutr. 2010 May;140(5):925-31. doi: 10.3945/jn.109.116822. Epub 2010 Mar 24.
Neonates with intrauterine growth restriction (IUGR) are prone to suffer from digestive diseases. Using neonatal pigs with IUGR, we tested the hypothesis that IUGR may induce alterations in the developmental pattern of intestinal barrier and thereby may be responsible for IUGR-associated increased morbidity. Piglets with a birth weight near the mean birth weight (+/-0.5 SD) were identified as normal birth weight (control) and piglets with a mean -2 SD lower birth weight (-30%) were defined as piglets with IUGR. The developmental pattern of intestinal structure, transcriptomic profile, and bacterial colonization was investigated from birth to d 5 postnatal. At birth, intestinal weight and length, ileal and colonic weight per unit of length, and villous sizes were lower (P < 0.05) in piglets with IUGR than in same-age control piglets. These IUGR-induced intestinal alterations further persisted, although they were less marked at d 5. Counts of adherent bacteria to ileal and colonic mucosa were greater (P < 0.05) in 2-d-old piglets with IUGR than in same-age control piglets. Dynamic analyses of the transcriptomic profile of the intestine revealed molecular evidence of IUGR-induced intestinal growth impairment that may result from a change in the cell proliferation-apoptosis balance during the first days of life, while a protective process would occur later on. In addition, changes in the expression of several genes suggest a pivotal role of both glucocorticoids and microbiota in driving IUGR intestinal development during the neonatal period.
宫内生长受限(IUGR)的新生儿易患消化系统疾病。我们使用患有 IUGR 的新生仔猪来检验以下假设,即 IUGR 可能会改变肠道屏障的发育模式,从而导致与 IUGR 相关的发病率增加。出生体重接近平均出生体重(+/-0.5 SD)的仔猪被确定为正常出生体重(对照),而出生体重平均低 2 SD(-30%)的仔猪被定义为 IUGR 仔猪。从出生到出生后第 5 天,研究了肠道结构、转录组谱和细菌定植的发育模式。出生时,IUGR 仔猪的肠道重量和长度、回肠和结肠单位长度的重量以及绒毛大小均低于同龄对照仔猪(P < 0.05)。尽管在第 5 天这些 IUGR 引起的肠道改变仍持续存在,但程度较轻。2 日龄 IUGR 仔猪回肠和结肠黏膜黏附细菌的数量多于同龄对照仔猪(P < 0.05)。肠道转录组谱的动态分析提供了 IUGR 诱导的肠道生长受损的分子证据,这可能是由于生命最初几天细胞增殖-凋亡平衡的改变所致,而稍后会发生保护过程。此外,几个基因表达的变化表明,糖皮质激素和微生物群在驱动新生儿期 IUGR 肠道发育中起关键作用。