Integrating Metabolomics and Transcriptomics to Analyse and Reveal the Regulatory Mechanisms of Mung Bean Polyphenols on Intestinal Cell Damage Under Different Heat Stress Temperatures

Nutrients. 2024 Dec 29;17(1):88. doi: 10.3390/nu17010088.

Abstract

Background/objectives: Polyphenols represent a new strategy of dietary intervention for heat stress regulation.

Methods: The metabolic and genetic effects of three heat stress-regulated mung bean polyphenols on mouse small intestinal epithelial Mode-k cells were investigated by metabolomics-transcriptomics correlation analysis at different heat stress levels.

Results: Lipid metabolism, energy metabolism, and nervous system pathways were the key metabolic regulatory pathways. Under the heat stresses of 39 °C, 41 °C, and 43 °C, the key pathways regulated by mung bean polyphenols on intestinal epithelial Mode-k cells were choline metabolism, pyrimidine metabolism, and the retrograde endorphin signalling pathway in cancer, respectively. FoxO, Rap1, and PI3K-Akt signalling pathways were the key environmental regulatory signalling pathways. Mung bean polyphenols can alleviate heat stress-induced cells at 39 °C by inhibiting cell apoptosis and promoting lipid and amino acid accumulation. Mung bean polyphenols can alleviate the threat of cell death caused by heat stress at 41 °C by regulating heat shock proteins, inhibiting mitochondrial function and some nerve disease-related genes. The threat of cell death by heat stress at 43 °C can be alleviated by regulating nerve-related genes.

Conclusions: This study confirmed that mung bean polyphenols can regulate heat stress. The results provide a reference for analysing the mechanism of dietary polyphenol regulating heat stress.

Keywords: gut; heat stress; mechanism; multi-omics; mung bean polyphenols.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cell Line
  • Gene Expression Profiling
  • Heat-Shock Response* / drug effects
  • Hot Temperature
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / metabolism
  • Lipid Metabolism / drug effects
  • Metabolomics*
  • Mice
  • Polyphenols* / pharmacology
  • Signal Transduction / drug effects
  • Transcriptome / drug effects
  • Vigna*

Substances

  • Polyphenols