A novel rat model of inflammatory bowel disease developed using a device created with a 3D printer.

2,4,6-trinitrobenzene sulphonic acid 3D printer Allogeneic adipose-derived mesenchymal stem cells IBD models Mesalazine Prednisolone

Journal

Regenerative therapy
ISSN: 2352-3204
Titre abrégé: Regen Ther
Pays: Netherlands
ID NLM: 101709085

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 06 10 2019
revised: 03 12 2019
accepted: 05 12 2019
entrez: 24 1 2020
pubmed: 24 1 2020
medline: 24 1 2020
Statut: epublish

Résumé

Inflammatory bowel disease (IBD) is an intractable condition. Existing models of experimental IBD are limited by their inability to create consistent ulcers between animals. The aim of this study was to develop a novel model of experimental colitis with ulcers of reproducible size. We used a 3D printer to fabricate a novel device containing a small window (10 × 10 mm) that could be inserted rectally to facilitate the creation of a localized ulcer in the rat intestinal mucosa. The mucosa within the window of the device was exposed to 2,4,6-trinitrobenzene sulfonic acid (TNBS) to generate ulceration. We evaluated the effects of conventional drug therapies (mesalazine and prednisolone) and local transplantation of allogeneic adipose-derived mesenchymal stem cells (ASCs) on ulcer size (measured from photographic images using image analysis software) and degree of inflammation (assessed histologically). The novel method produced localized, circular or elliptical ulcers that were highly reproducible in terms of size and depth. The pathological characteristics of the lesions were similar to those reported previously for conventional models of TNBS-induced colitis that show greater variation in ulcer size. Ulcer area was significantly reduced by the administration of mesalazine or prednisolone as an enema or localized injection of ASCs. The new model of TNBS-induced colitis, made with the aid of a device fabricated by 3D printing, generated ulcers that were reproducible in size. We anticipate that our new model of colitis will provide more reliable measures of treatment effects and prove useful in future studies of IBD therapies.

Identifiants

pubmed: 31970267
doi: 10.1016/j.reth.2019.12.005
pii: S2352-3204(19)30163-4
pmc: PMC6961759
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1-10

Informations de copyright

© 2020 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V.

Déclaration de conflit d'intérêts

The authors have declared that there is no conflict of interest.

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Auteurs

Tomoko Kuriyama (T)

Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women's Medical University, Shinjyuku, Tokyo, 162-8666, Japan.

Masayuki Yamato (M)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Shinjyuku, Tokyo, 162-8666, Japan.

Jun Homma (J)

Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, Shinjyuku, Tokyo, 162-8666, Japan.

Yusuke Tobe (Y)

Department of Integrative Bioscience and Biomedical Engineering, Graduate School of Advanced Science and Engineering, TWIns, Waseda University, Shinjyuku, Tokyo, 162-8480, Japan.

Katsutoshi Tokushige (K)

Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women's Medical University, Shinjyuku, Tokyo, 162-8666, Japan.

Classifications MeSH