首页> 外文期刊>International journal of molecular medicine >Astragalus polysaccharides exert protective effects in newborn rats with bronchopulmonary dysplasia by upregulating the expression of EGFL7 in lung tissue
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Astragalus polysaccharides exert protective effects in newborn rats with bronchopulmonary dysplasia by upregulating the expression of EGFL7 in lung tissue

机译:黄芪多糖可通过上调肺组织EGFL7的表达对新生的支气管肺发育不良大鼠起到保护作用

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The aim of this study was to explore the effects of Astragalus polysaccharides (APS) on the mRNA expression of epidermal growth factor-like domain 7 (EGFL7) in lung tissue in newborn rats with bronchopulmonary dysplasia (BPD). For this purpose, a total of 96?newborn SD rats were randomly divided into 4?groups (n=24): the control group, air room plus APS group, BPD group and the APS group (20?mg/kg/day). Lung tissues were obtained on days 4, 10 and 14 after birth. Morphological changes were observed and the protein and mRNA expression levels of EGFL7, Bax and Bcl-2 were determined. The rats in the BPD group (BPD induced by hyperoxia) presented with an arrest in alveolar and vascular development and low mRNA and protein expression levels of of EGFL7, Bcl-2 and high levels of Bax compared with the rats in the control group. However, lung damage in the APS intervention group was attenuated compared with the BPD group. The protein and mRNA expression levels of EGFL7 and Bcl-2 were also increased and the level of Bax was decreased in the APS intervention group (P<0.01) compared with the BPD model group after birth on days?4, 10 and?14. Our data demonstrate that APS reduce airway remodeling and alveolar damage by upregulating the expression of EGFL7 and exert protective effects against BPD in neonatal rats. Thus, APS may have potential for use as a therapeutic strategy for BPD.
机译:这项研究的目的是探讨黄芪多糖(APS)对支气管肺发育不良(BPD)新生大鼠肺组织中表皮生长因子样结构域7(EGFL7)mRNA表达的影响。为此,将96只新生SD大鼠随机分为4组(n = 24):对照组,气室加APS组,BPD组和APS组(20?mg / kg /天)。 。出生后第4、10和14天获得肺组织。观察形态变化并测定EGFL7,Bax和Bcl-2的蛋白质和mRNA表达水平。与对照组相比,BPD组(高氧诱导的BPD)大鼠的肺泡和血管发育停滞,EGFL7,Bcl-2的mRNA和蛋白表达水平较低,而Bax的表达水平较高。但是,与BPD组相比,APS干预组的肺损伤有所减轻。在出生后第4、10和14天,与BPD模型组相比,APS干预组的EGFL7和Bcl-2的蛋白质和mRNA表达水平也升高,而Bax水平降低(P <0.01)。我们的数据表明,APS通过上调EGFL7的表达并减轻新生大鼠BPD的保护作用来减少气道重塑和肺泡损伤。因此,APS可能有潜力用作BPD的治疗策略。

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