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A Phosphodiesterase Type-5 (PDE-5) Inhibitor, Sildenafil, Ameliorates the NEC Induced Inflammation
Mehmet Akif Ovalı1, Özlem Öztopuz2, İhsan Karaboğa3
1Faculty of Medicine, Department of Physiology, Çanakkale Onsekiz Mart University, Çanakkale, Turkey. maovali@comu.edu.tr.
Insights
Sildenafil treatment reduced inflammation and lung tissue damage in a neonatal rat model of necrotizing enterocolitis (NEC). This finding highlights sildenafil's therapeutic potential for gut-lung axis disorders.
Area of Science:
- Neonatology
- Pulmonology
- Gastroenterology
Background:
- The gut-lung axis describes the relationship between the gut microbiota and lung diseases, impacting homeostasis and disease.
- Necrotizing enterocolitis (NEC) is a critical gastrointestinal complication in newborns, often accompanied by pulmonary issues causing significant morbidity.
Purpose of the Study:
- To investigate the therapeutic effects of sildenafil on lung tissue inflammation and histopathological alterations in a neonatal rat model of experimental necrotizing enterocolitis.
Main Methods:
- Neonatal Wistar Albino rats were divided into control, NEC, and varying sildenafil dose groups.
- NEC was induced via hypoxia/asphyxia and cold stress.
- Lung tissues were analyzed for histopathological changes (H&E, Masson trichrome staining) and mRNA expression of TNF-α, IL-6, and HSPa5.
Main Results:
- NEC group showed increased mRNA levels of TNF-α, IL-6, and HSPa5 compared to controls.
- Sildenafil treatment significantly reduced these inflammatory markers and associated lung tissue damage (edema, hemorrhage).
- Histopathological findings showed reduced alveolar and interstitial edema and hemorrhage in sildenafil-treated groups.
Conclusions:
- Sildenafil demonstrates a therapeutic effect on NEC-induced lung inflammation at both molecular and tissue levels.
- The findings suggest sildenafil's potential as a treatment for lung complications associated with NEC.
- This study underscores the therapeutic potential of targeting the gut-lung axis in neonatal critical illnesses.
Abstract:
The connection between intestine microbiota and lung disease is described as the gut-lung axis, these organ systems are somehow interrelated in both homeostasis and disease development. In newborns, the most important gastrointestinal complications are necrotizing enterocolitis (NEC), and the pulmonary complication both cause significant systemic morbidity. In this study, sildenafil administered at varying doses in neonatal rat model of experimental necrotizing enterocolitis and focused on both mRNA expression and histopathological alterations. 15-day-old Wistar Albino rat pups were randomly divided into six groups; Control, NEC, DMSO, Sil_1mg, Sil_5mg, Sil_10mg (n = 5). NEC induction was performed using hypoxia/asphyxia and cold stress. At the end of the experiment, lung tissues were harvested, molecular and histopathological alterations were analysed. Histopathological examination was performed with hematoxylin&eosin and masson trichrome staining in lung samples of neonatal rats and the mRNA expression levels of TNF-α, IL-6 and HSPa5 genes were analyzed. The mRNA expression levels of TNF-α, IL-6 and HSPa5 were increased in the NEC group compared to the control group and sildenafil treatment could significantly reduced the levels of the genes and inflammation (*p < 0.05 and **p ≤ 0.0001). Alveolar edema and hemorrhage findings were observed in the lung tissue of the NEC group. Interstitial edema and hemorrhage findings were reduced in the groups treated with sildenafil compared to the NEC group. The data we obtained indicate that sildenafil administering at different doses has therapeutic effect on NEC induced lung tissue inflammation both at the mRNA expression and tissue levels.
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