Comparative lobe-specific histomorphometric evaluation of pulmonary architecture, fibrosis, and alveolar macrophage distribution in swine raised under different management systems
Nattawat Chaiyawong, Napat Praditwattanakit, Surachai Chamsodsai, Pichaya Jumnongprakhon, Ittipon Phoungpetchara, Charkriya Promsuban

TL;DR
This study compares lung structure and health in pigs raised under different management systems, finding that free-range pigs have healthier lungs while beta-agonist-free rearing leads to more fibrosis and inflammation.
Contribution
The study provides the first quantitative, lobe-specific histomorphometric comparison of pulmonary remodeling in swine under different management systems.
Findings
Beta-agonist-free rearing pigs showed thicker alveolar walls, higher fibrosis, and increased macrophage density in middle and caudal lobes.
Free-range pigs exhibited preserved pulmonary architecture with thinner alveolar septa and lower fibrosis indices.
Hygienic management resulted in intermediate lung parameters, suggesting balanced structural adaptation.
Abstract
Swine housing and management systems strongly influence respiratory health through their effects on air quality, ventilation, and environmental exposure. However, quantitative, lobe-specific evidence describing how different management systems affect pulmonary microarchitecture remains limited. This study aimed to compare alveolar structure, fibrosis, collagen deposition, and alveolar macrophage distribution in swine raised under hygienic, beta-agonist-free rearing, and free-range systems. Fifteen clinically healthy male crossbred (Large White × Landrace) swine were allocated to three management systems (n = 5 per group): hygienic, beta-agonist-free rearing, and free-range. Lung samples were collected from the right cranial, middle, and caudal lobes following humane slaughter. Sections were stained with Masson’s trichrome for collagen visualization. Quantitative histomorphometric…
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Taxonomy
TopicsInterstitial Lung Diseases and Idiopathic Pulmonary Fibrosis · Inhalation and Respiratory Drug Delivery · Indoor Air Quality and Microbial Exposure
