# Modulating Gut–System Axis Metabolic Disorders: Multi-Omics Reveals the Mechanism of Mung Bean Polyphenols in Alleviating Heat Stress-Induced Damage

**Authors:** Ying Li, Shu Zhang, Tianxin Fu, Yuchao Feng, Changyuan Wang

PMC · DOI: 10.3390/foods15050902 · Foods · 2026-03-05

## TL;DR

This study shows how mung bean polyphenols protect against heat stress by improving gut and systemic metabolism and reducing inflammation.

## Contribution

The novel contribution is the use of multi-omics to reveal how mung bean polyphenols alleviate heat stress through a gut-derived protective metabolic axis.

## Key findings

- Mung bean polyphenols reversed heat stress-induced oxidative stress and inflammation in mice.
- Key metabolic pathways like arachidonic acid and tryptophan metabolism were central to the protective effects.
- Indolelactic Acid and other hub metabolites correlated with improved physiological outcomes.

## Abstract

Heat stress-induced systemic metabolic disorder serves as the core pathological basis of organismal damage. Although mung bean polyphenols (MBPs) had been preliminarily validated in cellular heat-stress models for their intestinal tissue-protective potential, whether they can alleviate heat-stress injury in vivo by remodeling the metabolic crosstalk network between the gut and systemic circulation remains mechanistically unclear. In this study, we innovatively employed an integrated multi-omics approach combining physiological phenotype, gut metabolome, and serum metabolome analyses based on a Balb/c heat stress (41 °C) mouse model, systematically constructing the metabolic phenotype regulatory network of MBPs. The results demonstrated that MBPs not only significantly improved oxidative stress (elevating GSH-Px and T-AOC, reducing MDA), immune-inflammation (down-regulating IL-1β and TNF-α), and stress hormone (lowering cortisol) phenotypes, but also specifically reversed the disturbances in intestinal and serum metabolic profiles induced by heat stress, particularly restoring key pro-inflammatory mediators such as Leukotriene E4 and 5-HETE. Arachidonic acid metabolism, tryptophan metabolism, histidine metabolism, and Fc epsilon RI signaling pathway constituted the core network of heat-stress metabolic disorder and MBP regulation. Furthermore, the study revealed that alterations in hub metabolites—Indolelactic Acid, Trans-Cinnamic Acid, Leukotriene E4, 5-HETE, and N(omega)-Hydroxyarginine—were significantly correlated with phenotypic improvements. This confirms that mung bean polyphenols dynamically dismantle the “pro-inflammatory-oxidative stress” pathological coupling by constructing a novel protective axis centered on the indole metabolism–melatonin–endogenous antioxidant system and successfully established a novel protective axis driven by gut-derived beneficial metabolites that promotes systemic antioxidant function, thereby elucidating the systemic mechanism underlying the alleviation of heat-stress injury at the metabolic network level.

## Linked entities

- **Chemicals:** Leukotriene E4 (PubChem CID 5280879), 5-HETE (PubChem CID 1771), Indolelactic Acid (PubChem CID 92904), Trans-Cinnamic Acid (PubChem CID 444539), N(omega)-Hydroxyarginine (PubChem CID 123895)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), Metabolic Disorders (MESH:D008659)
- **Chemicals:** Polyphenols (MESH:D059808), histidine (MESH:D006639), N(omega)-Hydroxyarginine (MESH:C068309), MDA (MESH:D015104), tryptophan (MESH:D014364), melatonin (MESH:D008550), Indolelactic Acid (MESH:C024139), Trans-Cinnamic Acid (MESH:C029010), cortisol (MESH:D006854), Arachidonic acid (MESH:D016718), Leukotriene E4 (MESH:D017999), 5-HETE (MESH:C022022)
- **Species:** Vigna radiata (mung bean, species) [taxon 157791], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984524/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984524/full.md

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Source: https://tomesphere.com/paper/PMC12984524