Why the study?
The renin-angiotensin system modulates fibrosis, a common complication of ileal Crohn's disease, but the efficacy of losartan to treat intestinal fibrosis required testing in preclinical models.
Does losartan reduce inflammation and fibrosis in preclinical models of Crohn's-like disease?
Does losartan reduce inflammation and fibrosis in preclinical models of Crohn's-like disease?
Losartan reduces inflammation and fibrosis in preclinical models of Crohn's disease, suggesting a potential therapeutic role for targeting the renin-angiotensin system in intestinal fibrosis.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for RAS blockade in intestinal fibrosis; human trials needed before clinical consideration.
BACKGROUND AND AIMS: The renin-angiotensin system (RAS) is known to modulate fibrosis, which is a common complication of ileal Crohn's disease. We tested the efficacy of losartan, an angiotensin receptor blocker, to treat intestinal fibrosis in relevant preclinical models of Crohn's-like disease. METHODS: Effector molecules of the RAS were mined in a large publicly available RNA-Seq dataset of intestinal biopsies from Crohn's patients and healthy individuals, and the presence of associated proteins was confirmed by immunohistochemistry in full-thickness intestinal tissues. Losartan's efficacy in altering mediators of the RAS and of fibrosis was tested in vitro using activated CCD-18Co fibroblasts, while its in vivo effects were investigated by administering losartan to SAMP1/YitFc (SAMP) mice, a well-described model of Crohn's-like disease that progressively develops both ileal-specific inflammation and fibrosis, using either therapeutic or maintenance of remission (treatment after dexamethasone) approaches. RESULTS: Angiotensinogen, an upstream regulator of the RAS, and the downstream effector, angiotensin II receptor type 1, expressed on target cells, are both increased in involved vs non-involved gut mucosa from Crohn's patients compared to healthy controls. In vitro, losartan suppresses the expression of molecules related to fibrosis, fibroblast-to-myofibroblast differentiation, collagen deposition, and cytoskeletal alterations. In vivo, losartan decreases both inflammation and fibrosis in SAMP mice with established disease, and prevents the reoccurrence of fibrosis following a novel relapse protocol. CONCLUSIONS: Losartan, and other drugs targeting the RAS, may serve as an effective treatment to successfully dampen intestinal fibrosis during active inflammation, as well as prevent its progression after corticosteroid-induced remission in Crohn's patients.
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Artone et al. (2025) studied this question.
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