Abstract

We aimed to investigate the effect of chronic particulate matter (PM) exposure on bleomycin-induced lung fibrosis in a rat model using chest CT, histopathologic evaluation, and RNA-sequencing. A bleomycin solution was intratracheally administrated to 20 male rats. For chronic PM exposure, after four weeks of bleomycin treatment to induce lung fibrosis, PM suspension (experimental group) or normal saline (control group) was intratracheally administrated for 10 weeks. Chest CT was carried out in all rats, and then both lungs were extracted for histopathologic evaluation. One lobe from three rats in each group underwent RNA sequencing, and one lobe from five rats in each group was evaluated by western blotting. Inflammation and fibrosis scores in both chest CT and pathologic analysis were significantly more aggravated in rats with chronic PM exposure than in the control group. Several genes associated with inflammation and immunity were also upregulated with chronic PM exposure. Our study revealed that chronic PM exposure in a bleomycin-induced lung fibrosis rat model aggravated pulmonary fibrosis and inflammation, proven by chest CT, pathologic analysis, and RNA sequencing.

Highlights

  • We aimed to investigate the effect of chronic particulate matter (PM) exposure on bleomycin-induced lung fibrosis in a rat model using chest computed tomography (CT), histopathologic evaluation, and RNA-sequencing

  • The present study showed that chronic PM exposure aggravated pulmonary fibrosis and inflammation underlying bleomycin-induced lung fibrosis, as proven by chest CT, pathological analysis, and RNA sequencing

  • Several genes associated with inflammation and immunity were upregulated in a bleomycin-induced lung fibrosis rat model with chronic PM exposure

Read more

Summary

Introduction

We aimed to investigate the effect of chronic particulate matter (PM) exposure on bleomycin-induced lung fibrosis in a rat model using chest CT, histopathologic evaluation, and RNA-sequencing. Inflammation and fibrosis scores in both chest CT and pathologic analysis were significantly more aggravated in rats with chronic PM exposure than in the control group. Our study revealed that chronic PM exposure in a bleomycin-induced lung fibrosis rat model aggravated pulmonary fibrosis and inflammation, proven by chest CT, pathologic analysis, and RNA sequencing. Recent research evaluated polyhexamethylene guanidine (PHMG)‐induced lung injuries by chest C­ T12,13 In these studies, CT findings of lung inflammation and fibrosis due to PHMG were well correlated with pathological findings, proving the usefulness of chest CT in the evaluation of lung lesions in a rat model. There have been few papers verifying the pulmonary effects of PM using chest CT in both experimental animals and humans

Objectives
Methods
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call