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
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

59-67

Subventions

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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Auteurs

Savas Theodore Tsikis (ST)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

Scott C Fligor (SC)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

Jordan D Secor (JD)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

Lumeng J Yu (LJ)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

Amy Pan (A)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

Greta Loring (G)

Alcresta Therapeutics, Newton, Massachusetts.

Eric First (E)

Alcresta Therapeutics, Newton, Massachusetts.

Arthur P Nedder (AP)

Animal Care Resources Children's Hospital, Boston Children's Hospital, Boston, Massachusetts.

Robin M Grammer (RM)

Animal Care Resources Children's Hospital, Boston Children's Hospital, Boston, Massachusetts.

Coral Rudie (C)

Department of Gastroenterology, Boston Children's Hospital, Boston, Massachusetts.

Kathleen M Gura (KM)

Department of Pharmacy and the Division of Gastroenterology and Nutrition, Boston Children's Hospital, Boston, Massachusetts.

Mark Puder (M)

Vascular Biology Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts; Department of Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts. Electronic address: Mark.Puder@childrens.harvard.edu.

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Classifications MeSH