Outcomes and Perioperative Nutritional Management in a Porcine Model of Short Bowel Syndrome.
Coefficient of fat absorption
Fat-soluble vitamins
Nutritional optimization
Porcine model
Short bowel syndrome
Steatorrhea
Journal
The Journal of surgical research
ISSN: 1095-8673
Titre abrégé: J Surg Res
Pays: United States
ID NLM: 0376340
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
03
08
2021
revised:
06
12
2021
accepted:
04
01
2022
pubmed:
6
2
2022
medline:
27
4
2022
entrez:
5
2
2022
Statut:
ppublish
Résumé
Short bowel syndrome (SBS) results from significant intestinal loss and is characterized by insufficient absorption of nutrients and fluids. Preclinical large animal SBS models typically require parenteral nutrition (PN) support and may not be appropriate for studying interventions to improve intestinal absorption or adaptation. Here, we describe the development of a porcine SBS model that does not require PN support. Eight male Yorkshire piglets underwent either a 75% or 90% jejunoileal resection (n = 5) or no resection (n = 3). Continuous enteral nutrition (EN) was provided via a gastrostomy tube. The final SBS model consisted of a 75% resection and nutrition provided via combination EN (60%) and per oral pig chow (40%). Body weight and concentration of fat-soluble vitamins were assessed on postoperative days (POD) 7, 14, and 21. For assessing fat malabsorption, the coefficient of fat absorption (CFA) was calculated following a 72-h stool collection. Resected animals had decreased weight gain compared to unresected controls (POD21 + 8.3% versus +28.8%, P = 0.048). Vitamin D concentration was significantly lower in resected animals compared to controls on POD 7, POD 14, and POD 21. Serum vitamin E concentration was also lower on POD 21. Resected animals developed fat malabsorption with lower CFA (76.5% versus 95.3%, P = 0.014). We describe the development of a porcine SBS model that does not require PN support. Piglets in this model gain less weight, demonstrate fat malabsorption, and develop fat-soluble vitamin deficiencies. This model will benefit investigations of intestinal absorption or adaptation while potentially decreasing costs and confounding complications related to PN administration.
Identifiants
pubmed: 35123284
pii: S0022-4804(22)00004-X
doi: 10.1016/j.jss.2022.01.004
pmc: PMC9038684
mid: NIHMS1772829
pii:
doi:
Substances chimiques
Vitamins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
59-67Subventions
Organisme : NIDDK NIH HHS
ID : T32 DK007754
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007734
Pays : United States
Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.
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