Background
Inflammatory bowel disease (IBD) consists of two chronic remitting-relapsing inflammatory disorders in the colon referred to as ulcerative colitis (UC) and Crohn’s disease (CD). IBD affects about 1.4 million Americans. TNBS (2,4,6-trinitrobenzene sulfonic acid)-induced colitis is a widely used model of experimental intestinal inflammation with characteristic transmural and segmental lesions that are similar to CD.
Methods
Here we report on the use of contrast-enhanced MRI (CE-MRI) to monitor in vivo bladder permeability changes resulting from bladder crosstalk following colon TNBS exposure, and TNBS-induced colitis. Changes in MRI signal intensities and histology were evaluated for both colon and bladder regions.
Key Results
Uptake of contrast agent in the colon demonstrated a significant increase in signal intensity (SI) for TNBS-exposed rats (p<0.01) compared to controls. Additionally, a significant increase in bladder SI for colon TNBS-exposed rats (p<0.001) was observed compared to saline controls. Histological damage within the colon was observed, however bladder histology indicated a normal urothelium in rats with TNBS-induced colitis, despite increased permeability seen by CE-MRI.
Conclusions & Inferences
CE-MRI was able to quantitatively measure inflammation associated with TNBS-induced colitis, as well as assess bladder crosstalk measured as an increase in urothelial permeability. Although CE-MRI is routinely used to assess inflammation with IBD, currently there is no diagnostic test to assess bladder crosstalk with this disease, and our developed method may be useful in providing crosstalk information between organ and tissue systems in IBD patients, in addition to colitis.