首页> 外文期刊>Pediatric Research >Effects of Probiotics, Prebiotics, and Synbiotics on Messenger RNA Expression of Caveolin-1, NOS, and Genes Regulating Oxidative Stress in the Terminal Ileum of Formula-Fed Neonatal Rats
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Effects of Probiotics, Prebiotics, and Synbiotics on Messenger RNA Expression of Caveolin-1, NOS, and Genes Regulating Oxidative Stress in the Terminal Ileum of Formula-Fed Neonatal Rats

机译:益生元,益生元和合生元对配方奶喂养的新生鼠终末回肠中小窝蛋白1,NOS和调节氧化应激基因的Messenger RNA表达的影响

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Necrotizing enterocolitis (NEC) afflicts extremely low birth weight neonates, and probiotics reduces its incidence and severity. NO is involved in the pathogenesis of NEC, and caveolin-1 regulates NO signaling. We tested the hypothesis that intestinal caveolin-1 and NOS are deficient in formula-fed neonatal rats and that supplementation with “Florastar Kids” and/or galacto-oligosaccharides and fructo-oligosaccharides preserves caveolin-1 and NOS. At birth (P0), neonatal rat pups were maternally fed or hand-gavaged with or without supplemented formula. Samples from the terminal ileum were analyzed for total NO metabolites, growth factors, and gene expression of caveolin-1, NOS isoforms, and antioxidants. Our data showed that formula feeding with and without supplementation resulted in significant growth restriction. Despite suboptimal nutrition, growth factors involved in intestinal repair and regeneration were increased in the neonatal rat ileum. Caveolin-1, endothelial NOS, and neuronal NOS were simultaneously down-regulated with formula feeding while inducible NOS was up-regulated. Superoxide dismutase and glutathione peroxidase were up-regulated with supplementation. These data provide a probable mechanism for the benefits of supplemented formula for decreasing the severity of NEC by preserving the antioxidant systems.Abbreviations: eNOS, endothelial NOS; FOS, fructo-oligosaccharides; GOS, galactoligosaccharides; GPX, glutathione peroxidase; iNOS, inducible NOS; NEC, necrotizing enterocolitis; nNOS, neuronal NO synthase; NOx, NO metabolites; O2?, superoxide anion; ROS, reactive oxygen species; SOD, superoxide dismutase
机译:坏死性小肠结肠炎(NEC)折磨了极低的新生儿体重,益生菌降低了其发病率和严重程度。 NO参与NEC的发病机制,而Caveolin-1调节NO信号传导。我们检验了以下假设:在配方喂养的新生大鼠中肠道小窝蛋白1和NOS不足,补充“ Florastar Kids”和/或低聚半乳糖和低聚果糖的氨基酸可保存小窝蛋白1和NOS。出生时(P0),母鼠喂食或手工喂食有或没有补充配方奶的新生幼崽。分析了来自回肠末端的样本中的总NO代谢物,生长因子以及Caveolin-1,NOS亚型和抗氧化剂的基因表达。我们的数据表明,添加和不添加配方奶粉都会导致明显的生长受限。尽管营养欠佳,但新生大鼠回肠中参与肠道修复和再生的生长因子却增加了。配方奶喂养同时下调了Caveolin-1,内皮型NOS和神经元NOS,而诱导型NOS则上调。超氧化物歧化酶和谷胱甘肽过氧化物酶通过补充被上调。这些数据为补充配方奶通过保留抗氧化剂系统降低NEC严重程度的益处提供了一种可能的机制。 FOS,低聚果糖; GOS,半乳糖低聚糖; GPX,谷胱甘肽过氧化物酶; iNOS,诱导型NOS; NEC,坏死性小肠结肠炎; nNOS,神经元一氧化氮合酶; NOx,NO代谢物; O 2是超氧阴离子; ROS,活性氧; SOD,超氧化物歧化酶

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