Pulmonary fibrosis is a
chronic disease.
Urotensin II (U-II) is a new
peptide with angiogenic and profibrotic features. Therefore, we aim to evaluate the antagonism of U-II with
palosuran in an animal model and plan to measure U-II,
endothelin-1 (ET-1), and transforming growth factor-β1 (TGF-β1) and their association with lung
fibrosis. Thirty Wistar male rats were used in the study and were divided into three groups: group 1, control; group 2,
bleomycin-induced lung
fibrosis group; and group 3,
bleomycin-induced lung
fibrosis with treatment
palosuran group. U-II level (nanograms per milliliter) was 2.957 ± 0.159 in group1, 3.188 ± 0.122 in group 2, and 2.970 ± 0.165 in group 3 (p = 0.002). The ET-1 level (picograms per milliliter) was 4.486 ± 0.376 in group 1, 9.086 ± 1.850 in group 2, and 4.486 ± 0.376 in group 3 (p < 0.001). The TGF-β1 (nanograms per milliliter) level was 73.143 ± 9.96 in group 1, 84.81 ± 4.73 in group 2, and 77.86 ± 5.77 in group 3 (p = 0.006). Finally, the
fibrosis score was 0.7 ± 0.48 in group 1, 4.4 ± 1.34 in group 2, and 3.2 ± 0.63 in group 3 (p < 0.001). There is a statistically significant positive relationship between
fibrosis scores and the UT-II, ET-1, and TGF-β1 levels of the experimental lung
fibrosis model. We believe U-II is an important mediator in lung
fibrosis models, and its antagonism with
palosuran could be a new treatment choice for interstitial lung
fibrosis, but further studies need to be conducted to verify the findings of the current study.