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益生菌、益生元和合生元对配方奶喂养的新生大鼠回肠末端小窝蛋白-1、NOS 和氧化应激相关基因 mRNA 表达的影响。

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.

机构信息

Department of Pediatrics, State University of New York, Downstate Medical Center, Brooklyn, New York 11203, USA. ad'

出版信息

Pediatr Res. 2010 May;67(5):526-31. doi: 10.1203/PDR.0b013e3181d4ff2b.

Abstract

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.

摘要

坏死性小肠结肠炎(NEC)影响极低出生体重儿,益生菌可降低其发病率和严重程度。NO 参与 NEC 的发病机制,小窝蛋白-1 调节 NO 信号。我们假设在配方奶喂养的新生大鼠中,肠道小窝蛋白-1 和 NOS 缺乏,并用“Florastar Kids”和/或半乳糖-低聚果糖和果糖-低聚果糖进行补充可以保留小窝蛋白-1 和 NOS。在出生时(P0),通过母体喂养或人工灌胃给新生大鼠仔鼠喂食或不喂食添加补充剂的配方奶。分析回肠末端的总 NO 代谢产物、生长因子以及小窝蛋白-1、NOS 同工型和抗氧化剂的基因表达。我们的数据表明,添加或不添加补充剂的配方奶喂养都会导致明显的生长受限。尽管营养状况不佳,但参与肠道修复和再生的生长因子在新生大鼠回肠中增加。小窝蛋白-1、内皮型 NOS 和神经元型 NOS 同时随配方奶喂养而下调,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随补充而上调。这些数据提供了一种可能的机制,即补充配方奶通过维持抗氧化系统来降低 NEC 的严重程度。

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