Bai Juan, Zhu Ying, Dong Ying
School of Food and Biological Engineering, Jiangsu University, Zhenjiang, 212013, China.
Genes Genomics. 2018 Jun;40(6):561-567. doi: 10.1007/s13258-017-0642-4. Epub 2018 Feb 20.
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 PRKCβ (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.
众所周知,肥胖会诱发肠道的病理变化,而富含复杂碳水化合物且在小肠中难以消化的饮食会改变大肠生态。本研究的目的是确定苦瓜粉(BMP)对肥胖大鼠结肠黏膜中整体基因表达模式的影响。给肥胖大鼠喂食高脂饮食,并在无BMP或有BMP的情况下处理8周。在实验结束时,通过RNA测序(RNA-Seq)分析确定结肠黏膜的全基因组表达谱。共鉴定出87个基因在两组之间存在差异表达(倍数变化> 1.2)。这些结果通过定量RT-PCR进一步验证,证实了RNA-Seq的高可靠性。有趣的是,发现结肠中与炎症和脂质代谢相关的差异表达基因被BMP下调。基因与前15条KEGG通路之间的网络显示,PRKCβ(蛋白激酶Cβ)和Pla2g2a(磷脂酶A2 IIA组)与周围的通路和基因强烈相互作用。结果表明,补充BMP可以通过改变肥胖大鼠的转录组谱来重塑结肠的关键功能。