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Updated: Jun 24, 2026

A Rat Model of Mild Intrauterine Hypoperfusion with Microcoil Stenosis
Published on: January 7, 2018
Intrauterine growth restriction alters postnatal colonic barrier maturation in rats
Pascale Fança-Berthon1, Catherine Michel, Anthony Pagniez
1UMR 1280, Physiologie des Adaptations Nutritionnelles, INRA, Université de Nantes, Nantes, France.
Insights
Intrauterine growth restriction (IUGR) impairs the development of the colonic mucus barrier. This long-term alteration in mucin expression may increase the risk of intestinal injury later in life.
Area of Science:
- Gastroenterology
- Developmental Biology
- Perinatal Medicine
Background:
- Intrauterine growth restriction (IUGR) is a significant cause of infant mortality and morbidity.
- IUGR is linked to an increased risk of necrotizing enterocolitis and potential long-term intestinal issues.
- Mucins and trefoil factor family 3 (TFF3) are crucial for maintaining the integrity and healing of the gut epithelium.
Purpose of the Study:
- To investigate the impact of IUGR on the maturation of the colonic mucosa.
- To determine if IUGR affects the expression of mucins and TFF3 in the developing colon.
Main Methods:
- IUGR was induced in pregnant rats via dietary protein restriction.
- Colonic mucosa maturation, mucin, and TFF3 expression were analyzed during postnatal development.
- Quantitative analysis included mRNA and protein levels, crypt depth, and crypt fission rates.
Main Results:
- Rats with IUGR exhibited reduced mucin 2 and TFF3 protein levels before weaning.
- Post-weaning, IUGR was associated with lower mucin 2 (mRNA and protein) and mucin 4 (mRNA) expression.
- IUGR led to reduced colonic crypt depth and an increased percentage of crypts in fission.
Conclusions:
- IUGR significantly impairs the development of the colonic mucus barrier.
- Long-term alterations in mucin expression are a consequence of IUGR.
- The compromised colonic barrier in IUGR may predispose individuals to both neonatal and adult colonic injury.
Abstract:
Intrauterine growth restriction (IUGR) is a leading cause of perinatal mortality and morbidity and increases the risk for necrotizing enterocolitis. We hypothesized that colonic barrier disruption could be responsible for intestinal frailty in infants and adults born with IUGR. Mucins and trefoil factor family 3 (TFF3) actively contribute to epithelium protection and healing. Our aim was to determine whether IUGR affects colonic mucosa maturation. IUGR was induced by dietary protein restriction in pregnant dams. Mucins and Tff3 expression and morphologic maturation of the colonic mucosa were followed during postnatal development of the offspring. Before weaning, mucin 2 and Tff3 protein levels were reduced in colonic mucosa of rats with IUGR compared with controls. After weaning, expression of mucin 2 (mRNA and protein) and mucin 4 (mRNA) were lower in colonic mucosa of rats with IUGR. At the same time, IUGR was associated with a reduction of crypt depth and a higher percentage of crypts in fission. We conclude that IUGR impairs mucus barrier development and is associated with long-term alterations of mucin expression. The lack of an efficient colonic barrier induced by IUGR may predispose to colonic injury not only in neonatal life but also in later life.

