Evaluation of the mixture "MagSelDex" for neuroprotection against offspring brain injury in endotoxin-induced chorioamnionitis: A Preliminary Study

H. Aşçı, M. Savran, Sıla Gülbağ Pınar, N. F. Karakuyu, O. Imeci, Mehmer Abdulkadir Sevük, M. Sezik, Özlem Özmen
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Abstract

Objective: Chorioamnionitis resulting from preterm labor leads to concurrent damage in both the placenta and fetal brain. This study aims to explore the impact of incorporating antioxidants and anti-inflammatory agents, specifically selenium (Sel) and dexpanthenol (Dex), into the standard magnesium (Mg) regimen, in mitigating this damage. Materials and Methods: A total of six pregnant rats were assigned to six distinct groups: control, lipopolysaccharide (LPS) (1 mg/kg, single intraperitoneal dose on day 17), Mg (60 mg/kg Mg, intraperitoneal), Mg+Sel (1 mg/kg, intraperitoneal), Mg+Dex (500 mg/kg, intraperitoneal), and Mg+Sel+Dex. On the 17th day of pregnancy, fetal brain and placenta tissues were harvested for histopathological examination and immunohistochemical evaluation of tumor necrosis factor-alpha (TNF-α) and neurofilament expression. Results: The histopathological assessment revealed LPS-induced hemorrhage and mild inflammatory cell infiltration in the placenta, and pronounced hyperemia along with minor hemorrhage in the fetal brain. The LPS group exhibited significantly elevated TNF-α expression in both placenta and fetal brain, coupled with reduced neurofilament expression in the fetal brain. In contrast, the groups treated with Mg alone and the combined Sel and Dex therapy exhibited moderate to substantial improvement in pathological findings across both tissues. The most notable enhancement was observed in the Mg+Sel+Dex group. Conclusion: Administration of Mg as a standalone treatment and the coadministration of Sel and Dex effectively shielded the placenta and fetal brain from LPS-triggered chorioamnionitis. However, the most prominent protective effect was observed in the Mg+Sel+Dex group.
评估 "MagSelDex "混合物在内毒素诱导的绒毛膜羊膜炎中对后代脑损伤的神经保护作用:初步研究
目的:早产引起的绒毛膜羊膜炎会导致胎盘和胎儿大脑同时受损。本研究旨在探讨在标准镁(Mg)疗法中加入抗氧化剂和抗炎药物(特别是硒(Sel)和右泛醇(Dex))对减轻这种损害的影响:将六只妊娠大鼠分为六个不同的组别:对照组、脂多糖(LPS)组(1 毫克/千克,第 17 天单次腹腔注射)、镁组(60 毫克/千克镁,腹腔注射)、镁+塞尔组(1 毫克/千克,腹腔注射)、镁+地塞米松组(500 毫克/千克,腹腔注射)和镁+塞尔+地塞米松组。妊娠第17天,采集胎儿脑组织和胎盘组织进行组织病理学检查,并对肿瘤坏死因子α(TNF-α)和神经丝表达进行免疫组化评估:组织病理学评估显示,LPS诱导胎盘出血和轻度炎症细胞浸润,胎儿大脑明显充血并伴有轻微出血。LPS 组胎盘和胎儿大脑中 TNF-α 表达明显升高,胎儿大脑中神经丝表达降低。相比之下,单用镁治疗组和联合使用Sel和Dex治疗组在两种组织的病理结果上都有适度到实质性的改善。Mg+Sel+Dex组的改善最为显著:结论:单独服用镁以及联合服用塞尔和地塞米松可有效保护胎盘和胎儿大脑免受LPS引发的绒毛膜羊膜炎的影响。然而,镁+塞尔+地塞米松组的保护作用最为显著。
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