AI Summary & Key Takeaways
AI InsightThe histopathology results supported the molecular results.Conclusion: In this experimental study, we demonstrated for the first time the positive effects of AGO onLPS-induced sepsis in lung tissue using molecular and histopathological methods, indicating that it contributesto the prevention of lung damage
📌 3 Key Takeaways
Abstract
Objective: We designed an experimental model of sepsis in rats to investigate the effects of agomelatine(AGO) on lung tissues using molecular and histopathological methods.Materials and Methods: In our experimental model, the 32 rats were divided into 4 groups: group 1: controlgroup (HEALTHY); group 2: lipopolysaccharide group (LPS); group 3: LPS plus 50 mg/kg AGO group (LPS +AGO50); and group 4: LPS plus 100 mg/kg AGO group (LPS + AGO100). An LPS-induced sepsis model wasperformed to replicate the pathology of sepsis. Rats from all 4 groups were killed after 12 hours, and theirlungs were quickly collected. To investigate the therapeutic strategy, we evaluated tumor necrosis factoralpha (TNF-α) and nuclear factor-kappa B (NF-κB) messenger RNA expressions by real-time polymerasechain reaction using molecular methods and lung tissue damage indicators using histopathological methods.Results: The expressions of TNF-α and NF-κB were reduced in the groups treated with AGO. The histopathology results supported the molecular results.Conclusion: In this experimental study, we demonstrated for the first time the positive effects of AGO onLPS-induced sepsis in lung tissue using molecular and histopathological methods, indicating that it contributesto the prevention of lung damage