# Integrated Analysis of Gut Microbiota and Metabolites in a Rat Necrotizing Enterocolitis Model

## TL;DR

This study uses a rat model to explore gut microbiota and metabolite changes in necrotizing enterocolitis, linking specific bacteria and inflammation to disease progression.

## Contribution

The study identifies novel microbiota-metabolite correlations and elevated proinflammatory cytokines in a rat model of NEC.

## Key findings

- NEC rats showed significant intestinal damage and inflammatory infiltration.
- Lactobacillus and Morganella were strongly correlated with specific metabolites in NEC.
- Proinflammatory cytokines like IL-1β, TNF-α, and IL-6 were elevated in NEC rats.

## Abstract

Necrotizing enterocolitis (NEC) is a critical gastrointestinal emergency in newborns, characterized by mucosal damage, gut microbial dysbiosis, and inflammation. This study aimed to identify differential gut microbiota and metabolites in NEC and examine their correlations.

A rat model of NEC was established using hypoxia–hyperoxia and cold stress. Histopathological analysis, liquid chromatography–mass spectrometry, and 16S rDNA sequencing were used to analyze intestinal contents and tissues. Proinflammatory cytokine concentrations were measured via enzyme-linked immunosorbent assay.

Necrotizing enterocolitis rats exhibited significant intestinal damage, including hemorrhage, edema, necrosis, and inflammatory infiltration (P < .05). Correlation analysis revealed strong associations between specific microbiota (e.g., Lactobacillus and Morganella) and metabolites, suggesting their involvement in NEC pathogenesis (P < .05). Furthermore, NEC rats had elevated proinflammatory cytokine levels, including interleukin-1β, tumor necrosis factor-α, and interleukin-6 (P < .05).

This study successfully established a rat model of NEC, highlighting key microbiota–metabolite correlations and increased proinflammatory cytokines, providing insights into NEC pathogenesis and potential therapeutic targets.