A review on chemical-induced inflammatory bowel disease models in rodents
Ulcerative colitis and Crohn's disease are a set of chronic, idiopathic, immunological and relapsing inflammatory disorders of the gastrointestinal tract referred to as inflammatory bowel disorder (IBD). Although the etiological factors involved in the perpetuation of IBD remain uncertain, deve...
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| Published in: | The Korean journal of physiology & pharmacology Vol. 18; no. 4; pp. 279 - 288 |
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| Main Authors: | , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Korea (South)
The Korean Physiological Society and The Korean Society of Pharmacology
01-08-2014
대한약리학회 |
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| Abstract | Ulcerative colitis and Crohn's disease are a set of chronic, idiopathic, immunological and relapsing inflammatory disorders of the gastrointestinal tract referred to as inflammatory bowel disorder (IBD). Although the etiological factors involved in the perpetuation of IBD remain uncertain, development of various animal models provides new insights to unveil the onset and the progression of IBD. Various chemical-induced colitis models are widely used on laboratory scale. Furthermore, these models closely mimic morphological, histopathological and symptomatical features of human IBD. Among the chemical-induced colitis models, trinitrobenzene sulfonic acid (TNBS)-induced colitis, oxazolone induced-colitis and dextran sulphate sodium (DSS)-induced colitis models are most widely used. TNBS elicits Th-1 driven immune response, whereas oxazolone predominantly exhibits immune response of Th-2 phenotype. DSS-induced colitis model also induces changes in Th-1/Th-2 cytokine profile. The present review discusses the methodology and rationale of using various chemical-induced colitis models for evaluating the pathogenesis of IBD. |
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| AbstractList | Ulcerative colitis and Crohn's disease are a set of chronic, idiopathic, immunological and relapsing inflammatory disorders of the gastrointestinal tract referred to as inflammatory bowel disorder (IBD). Although the etiological factors involved in the perpetuation of IBD remain uncertain, development of various animal models provides new insights to unveil the onset and the progression of IBD. Various chemical-induced colitis models are widely used on laboratory scale. Furthermore, these models closely mimic morphological, histopathological and symptomatical features of human IBD. Among the chemical-induced colitis models, trinitrobenzene sulfonic acid (TNBS)-induced colitis, oxazolone induced-colitis and dextran sulphate sodium (DSS)-induced colitis models are most widely used. TNBS elicits Th-1 driven immune response, whereas oxazolone predominantly exhibits immune response of Th-2 phenotype. DSS-induced colitis model also induces changes in Th-1/Th-2 cytokine profile. The present review discusses the methodology and rationale of using various chemical-induced colitis models for evaluating the pathogenesis of IBD. Ulcerative colitis and Crohn’s disease are a set of chronic, idiopathic, immunological and relapsinginflammatory disorders of the gastrointestinal tract referred to as inflammatory bowel disorder (IBD). Although the etiological factors involved in the perpetuation of IBD remain uncertain, developmentof various animal models provides new insights to unveil the onset and the progression of IBD. Variouschemical-induced colitis models are widely used on laboratory scale. Furthermore, these models closelymimic morphological, histopathological and symptomatical features of human IBD. Among thechemical-induced colitis models, trinitrobenzene sulfonic acid (TNBS)-induced colitis, oxazoloneinduced-colitis and dextran sulphate sodium (DSS)-induced colitis models are most widely used. TNBSelicits Th-1 driven immune response, whereas oxazolone predominantly exhibits immune response ofTh-2 phenotype. DSS-induced colitis model also induces changes in Th-1/Th-2 cytokine profile. Thepresent review discusses the methodology and rationale of using various chemical-induced colitismodels for evaluating the pathogenesis of IBD. KCI Citation Count: 129 |
| Author | Singh, Kavinder Jaggi, Amteshwar Singh Randhawa, Puneet Kaur Singh, Nirmal |
| AuthorAffiliation | Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India |
| AuthorAffiliation_xml | – name: Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India |
| Author_xml | – sequence: 1 givenname: Puneet Kaur surname: Randhawa fullname: Randhawa, Puneet Kaur organization: Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India – sequence: 2 givenname: Kavinder surname: Singh fullname: Singh, Kavinder organization: Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India – sequence: 3 givenname: Nirmal surname: Singh fullname: Singh, Nirmal organization: Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India – sequence: 4 givenname: Amteshwar Singh surname: Jaggi fullname: Jaggi, Amteshwar Singh organization: Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala 147002, India |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25177159$$D View this record in MEDLINE/PubMed https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001901131$$DAccess content in National Research Foundation of Korea (NRF) |
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| Keywords | Inflammatory bowel disease Oxazolone Acetic acid TNBS DSS |
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