β 3 ‐adrenoceptor agonism exerts lung protection in a rat model of bronchopulmonary dysplasia

Absract Background and Purpose Bronchopulmonary dysplasia (BPD) affects premature newborns, particularly those receiving supplemental oxygen therapy. Exposure of underdeveloped lungs to oxygen levels higher than the intrauterine environment causes oxidative stress, impairing alveolarisation, vascularisation and causing fibrosis. The β 3 ‐adrenoceptor could represent a promising target for BPD treatment because of its oxygen‐dependent regulation, ability to reduce oxidative stress and protection against intestinal hyperoxia‐induced damage. Experimental Approach In this study, neonatal rat pups were reared under hyperoxia for 2 weeks to induce a BPD‐like disease and treated with the β 3 ‐adrenoceptor agonist BRL37344 (1, 3 or 6 mg kg −1 ). Key Results Through oxidative stress, hyperoxia decreases pulmonary volume, impairs alveolarisation and vascularisation, and causes fibrosis and type II pneumocyte hyperplasia, thereby reducing survival rates. BRL37344 at 3 mg kg −1 counteracted these alterations, doubling survival rates. Conclusions and Implications Our findings demonstrate a new role for β 3 ‐adrenoceptors in protecting the lungs from hyperoxic injury, suggesting its pharmacological activation as a strategy for treating Bronchopulmonary dysplasia of prematurity and, possibly, other lung fibrosis‐related disorders.