» Articles » PMID: 31565540

Formula Feeding Predisposes Gut to NSAID-Induced Small Intestinal Injury

Overview
Date 2019 Oct 1
PMID 31565540
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: Breast feeding protects infants from many diseases, including necrotizing enterocolitis, peptic ulceration and infectious diarrhea. Conversely, maternal separation stress and Non-Steroidal Anti-Inflammatory Drugs (NSAID's) can induce intestinal injury and bleeding. This study aimed to evaluate in suckling rats if maternal separation/formula feeding leads to increased intestinal sensitivity to indomethacin (indo)-induced intestinal injury and to look at potential mechanisms involved.

Methods: Nine-day-old rats were dam-fed or separated/trained to formula-feed for 6 days prior to indo administration (5 mg/kg/day) or saline (control) for 3 days. Intestinal bleeding and injury were assessed by measuring luminal and Fecal Hemoglobin (Hob) and jejunal histology. Maturation of the intestine was assessed by measuring luminal bile acids, jejunal sucrase, serum corticosterone, and mRNA expression of ileal Apical Sodium-Dependent Bile Acid Transporter (ASBT).

Results: At 17 days, formula-fed indo-treated pups had a 2-fold increase in luminal Hb compared to formula-fed control pups and had evidence of morphological injury to the small intestinal mucosa as observed at the light microscopic level, whereas indo had no effect on dam-fed littermates. In addition, formula-fed rats had significant increases in luminal bile acid, sucrase specific activity, serum corticosterone, and expression of ASBT mRNA compared to dam-fed rats.

Conclusion: Maternal separation stress may cause early intestinal maturational changes induced by corticosteroid release, including increased epithelial exposure to bile acids. These maturational changes may have a sensitizing rather than protective effect against indo-induced injury in the new-born.

Citing Articles

Metabolic immaturity and breastmilk bile acid metabolites are central determinants of heightened newborn vulnerability to norovirus diarrhea.

Peiper A, Morales Aparicio J, Hu Z, Phophi L, Helm E, Rubinstein R Cell Host Microbe. 2024; 32(9):1488-1501.e5.

PMID: 39214086 PMC: 11392616. DOI: 10.1016/j.chom.2024.08.003.


Organic Solute Transporter α-β Protects Ileal Enterocytes From Bile Acid-Induced Injury.

Ferrebee C, Li J, Haywood J, Pachura K, Robinson B, Hinrichs B Cell Mol Gastroenterol Hepatol. 2018; 5(4):499-522.

PMID: 29930976 PMC: 6009794. DOI: 10.1016/j.jcmgh.2018.01.006.

References
1.
Henning S . Plasma concentrations of total and free corticosterone during development in the rat. Am J Physiol. 1978; 235(5):E451-6. DOI: 10.1152/ajpendo.1978.235.5.E451. View

2.
Whittle B . Mechanisms underlying intestinal injury induced by anti-inflammatory COX inhibitors. Eur J Pharmacol. 2004; 500(1-3):427-39. DOI: 10.1016/j.ejphar.2004.07.042. View

3.
Shneider B, Dawson P, Christie D, Hardikar W, Wong M, Suchy F . Cloning and molecular characterization of the ontogeny of a rat ileal sodium-dependent bile acid transporter. J Clin Invest. 1995; 95(2):745-54. PMC: 295543. DOI: 10.1172/JCI117722. View

4.
Caplan M, Hedlund E, Adler L, Hsueh W . Role of asphyxia and feeding in a neonatal rat model of necrotizing enterocolitis. Pediatr Pathol. 1994; 14(6):1017-28. DOI: 10.3109/15513819409037698. View

5.
Hwang S, Henning S . Ontogenic regulation of components of ileal bile acid absorption. Exp Biol Med (Maywood). 2001; 226(7):674-80. DOI: 10.1177/153537020222600713. View