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

Genes Genomics. 2018 Jun;40(6):561-567. doi: 10.1007/s13258-017-0642-4. Epub 2018 Feb 20.

Abstract

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.

Keywords: Bitter melon; Gene expression; Obesity; RNA-Seq.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Colon / drug effects
  • Colon / metabolism
  • Diet, High-Fat
  • Dietary Fats / pharmacology
  • Dietary Supplements
  • Gene Expression Profiling / methods
  • Inflammation / drug therapy
  • Inflammation / genetics
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Lipid Metabolism / drug effects
  • Momordica charantia / drug effects*
  • Momordica charantia / metabolism
  • Obesity / genetics*
  • Obesity / metabolism*
  • RNA / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Reproducibility of Results
  • Sequence Analysis, RNA
  • Transcriptome / drug effects

Substances

  • Dietary Fats
  • RNA