A Phosphodiesterase Type-5 (PDE-5) Inhibitor, Sildenafil, Ameliorates the NEC Induced Inflammation.

Mehmet Akif Ovalı, Özlem Öztopuz, İhsan Karaboğa
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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.

磷酸二酯酶5型(PDE-5)抑制剂西地那非改善NEC诱导的炎症。
肠道微生物群和肺部疾病之间的联系被描述为肠-肺轴,这些器官系统在体内平衡和疾病发展中都有一定的相关性。在新生儿中,最重要的胃肠道并发症是坏死性小肠结肠炎(NEC),肺部并发症均可引起显著的全身发病率。在这项研究中,西地那非以不同剂量给予新生大鼠实验性坏死性小肠结肠炎模型,并关注mRNA表达和组织病理学改变。15日龄Wistar白化大鼠幼崽随机分为6组;对照,NEC, DMSO, Sil_1mg, Sil_5mg, Sil_10mg (n = 5)。采用缺氧/窒息和冷应激诱导NEC。在实验结束时,采集肺组织,分析分子和组织病理学改变。采用苏木精伊红和马松三色染色对新生大鼠肺组织进行病理检查,分析TNF-α、IL-6和HSPa5基因mRNA表达水平。与对照组相比,NEC组TNF-α、IL-6和HSPa5 mRNA表达水平升高,西地那非治疗可显著降低这些基因表达水平和炎症反应(*p
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