Treatment with Alamandine Reduces Established Pulmonary Fibrosis: Preliminary Histological, Functional, and Biochemical Insights
Pulmonary fibrosis (PF) is a challenging interstitial lung disease with limited therapeutic options. This study explores the therapeutic effects of alamandine (ALA), a renin-angiotensin system peptide, in reversing established fibrotic progression in an experimental model. Male Wistar rats were divided into four groups...