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Obese rats supplemented with bitter melon display marked shifts in the expression of genes controlling inflammatory response and lipid metabolism by RNA-Seq analysis of colonic mucosa

机译:补充有苦瓜显示器的肥胖大鼠标记为Colonal粘膜的RNA-SEQ分析控制炎症反应和脂质代谢的基因表达的变化

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摘要

Obesity is known to induce pathological changes in the gut and diets rich in complex carbohydrates that resist digestion in the small bowel can alter large bowel ecology. The purposes of this study were to identify the effects of bitter melon powder (BMP) on the global gene expression pattern in the colon mucosa of obese rats. Obese rats were fed a high-fat diet and treated without or with BMP for 8 weeks. Genome-wide expression profiles of the colon mucosa were determined by RNA sequencing (RNA-Seq) analysis at the end of experiment. A total of 87 genes were identified as differentially expressed (DE) between these two groups (fold change 1.2). These results were further validated by quantitative RT-PCR, confirming the high reliability of the RNA-Seq. Interestingly, DE genes implicated in inflammation and lipid metabolism were found to be downregulated by BMP in the colon. Network between genes and the top 15 KEGG pathways showed that PRKC beta (protein kinase C beta) and Pla2g2a (phospholipase A2 group IIA) strongly interacted with surrounding pathways and genes. Results revealed that BMP supplement could remodel key colon functions by altering transcriptomic profile in obese rats.
机译:已知肥胖是诱导富含碳水化合物的肠道和饮食中的病理变化,使小肠中的抗蚀剂消化可以改变大肠生态。该研究的目的是鉴定苦瓜粉(BMP)对肥胖大鼠结肠粘膜全球基因表达模式的影响。肥胖的大鼠喂养高脂饮食并没有或BMP治疗8周。通过在实验结束时通过RNA测序(RNA-SEQ)分析测定结肠粘膜的基因组表达谱。将总共​​87个基因鉴定为差异表达(DE)在这两组之间(折叠变化& 1.2)。通过定量RT-PCR进一步验证了这些结果,证实了RNA-SEQ的高可靠性。有趣的是,将涉及炎症和脂质代谢的DE基因被发现通过BMP在结肠中下调。基因之间的网络和前15个Kegg途径显示,PRKCβ(蛋白激酶Cβ)和PLA2G2A(磷脂酶A2 IIa)强烈地与周围途径和基因相互作用。结果表明,BMP补充剂可以通过改变肥胖大鼠的转录组概况来改造关键结肠作用。

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