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首页> 外文期刊>The Journal of Nutritional Biochemistry >Aberrant expression of microRNA induced by high-fructose diet: implications in the pathogenesis of hyperlipidemia and hepatic insulin resistance
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Aberrant expression of microRNA induced by high-fructose diet: implications in the pathogenesis of hyperlipidemia and hepatic insulin resistance

机译:高果糖饮食诱导微小瘤的异常表达:高脂血症和肝胰岛素抵抗力发病机制的影响

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摘要

Fructose is a highly lipogenic sugar that can alter energy metabolism and trigger metabolic disorders. In the current study, microRNAs (miRNAs) altered by a high-fructose diet were comprehensively explored to elucidate their significance in the pathogenesis of chronic metabolic disorders. miRNA expression profiling using small noncoding RNA sequencing revealed that 19 miRNAs were significantly upregulated and 26 were downregulated in the livers of high-fructose-fed mice compared to chow-fed mice. Computational prediction and functional analysis identified 10 miRNAs, miR-19b-3p, miR-101a-3p, miR-30a-5p, miR-223-3p, miR-378a-3p, miR-33-5p, miR-145a-3p, miR-128-3p, miR-125b-5p and miR-582-3p, assembled as a regulatory network to potentially target key genes in lipid and lipoprotein metabolism and insulin signaling at multiple levels. qRT-PCR analysis of their potential target genes [IRS-1, FOXO1, SREBP-lc/2, ChREBP, insulin-induced gene-2 (Insig-2), microsomal triglyceride transfer protein (M1TP) and apolipoprotein B (apoB)] demonstrated that fructose-induced alterations of miRNAs were also reflected in mRNA expression profiles of their target genes. Moreover, the miRNA profile induced by high-fructose diet differed from that induced by high-fat diet, indicating that miRNAs mediate distinct pathogenic mechanisms in dietary-induced metabolic disorders. This study presents a comprehensive analysis of a new set of hepatic miRNAs, which were altered by high-fructose diet and provides novel insights into the interaction between miRNAs and their target genes in the development of metabolic syndrome. (C) 2017 Elsevier Inc. All rights reserved.
机译:果糖是一种高度脂肪糖,可以改变能量代谢并引发代谢障碍。在目前的研究中,全面探索了高果糖饮食改变的MicroRNA(miRNA)以阐明其在慢性代谢障碍发病机制中的重要性。使用小型非编码RNA测序的miRNA表达分析显示,与味肠喂食小鼠相比,将19 miRNA显着上调,并且在高果糖喂食小鼠的肝脏中下调。计算预测和功能分析鉴定了10 miRNA,miR-19b-3p,miR-101a-3p,miR-30a-5p,miR-223-3p,miR-378a-3p,miR-33-5p,miR-145a-3p MiR-128-3P,MIR-125B-5P和MIR-582-3P,作为调节网络组装,以在多个水平下潜在地靶向脂质和脂蛋白代谢和胰岛素信号传导的关键基因。 QRT-PCR分析它们的潜在靶基因[IRS-1,FOXO1,SREBP-LC / 2,CHREBP,胰岛素诱导的基因-2(INSIG-2),微粒体甘油三酯转移蛋白(M1TP)和载脂蛋白B(APOB)]证明果糖诱导的miRNA的改变也反映在其靶基因的mRNA表达谱中。此外,高果糖饮食诱导的miRNA谱不同于通过高脂饮食诱导的诱导,表明miRNA在膳食诱导的代谢紊乱中介导不同的致病机制。本研究提出了一种全面的肝脏miRNA综合分析,其被高果糖饮食改变,并在代谢综合征发展中提供了对miRNA和其靶基因之间的相互作用的新见解。 (c)2017年Elsevier Inc.保留所有权利。

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