Evidence map›Paper›PMID 42573889›Full record

ArticleTissue engineering and regenerative medicine2026

A Pilot Study for Establishing DSS-Induced Colitis Model in Minipigs.

Hye Won Park, Woon Kyu Lee

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Article in Tissue engineering and regenerative medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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2 authors.

Hye Won ParkLaboratory of Developmental Genetics, Department of Biomedical Sciences, School of Medicine, Inha University, Rm#321, 60th memorial hall, 100 Inha-ro, Michuhol-gu, Incheon, 22212, South Korea.ORCID http://orcid.org/0009-0000-5948-5960
Woon Kyu LeeLaboratory of Developmental Genetics, Department of Biomedical Sciences, School of Medicine, Inha University, Rm#321, 60th memorial hall, 100 Inha-ro, Michuhol-gu, Incheon, 22212, South Korea. wklee@inha.ac.kr.ORCID http://orcid.org/0000-0001-7281-6322

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUlcerative colitis (UC) is a chronic inflammatory bowel disease characterized by relapsing and remitting colonic mucosal inflammation. Rodent dextran sodium sulfate (DSS) induced colitis models are widely used but have limited translational relevance due to anatomical and physiological differences. As a pilot feasibility study, this work aimed to explore whether graded DSS administration could induce reproducible colitis-like features in minipigs.

methodsWe developed a pilot large-animal UC model using Sus scrofa minipigs. Eight male Micropigs® were divided into four groups, with three groups receiving DSS at 0.2, 0.4, or 0.8 g/kg/day for 7 days. Clinical signs, body weight, colon length, endoscopic evaluation, and histopathology were assessed.

resultsDSS administration induced dose-dependent UC features. Group 4 minipigs (0.8 g/kg/day) showed the most severe clinical manifestations, including diarrhea, anorexia, and lethargy. Colon length was reduced by 34% in Group 4 compared to controls. Endoscopy revealed progressive mucosal edema, hemorrhage, and erosions. Histopathological scoring confirmed severe inflammation, crypt loss, and ulceration in higher-dose groups. Dose-dependent trends were consistently observed across clinical signs, endoscopic findings, and histopathological features.

conclusionThis DSS-induced minipig colitis model replicates clinical, endoscopic, and histological hallmarks of human UC. As an exploratory pilot study, it provides proof-of-concept for minipigs as a translational platform for inflammatory bowel disease (IBD) research and therapeutic evaluation.

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Animal modelEndoscopyInflammatory bowel diseaseMinipigUlcerative colitis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.