# Xingnao Jiutan tablets modulate gut microbiota and gut microbiota metabolism to alleviate cerebral ischemia/reperfusion injury

**Authors:** Yanyan Chen, Jing Zhang, Xiaoran Hou, Shijiao Cai, Jingyue Zhang, Yidan Gou, Hanxu Zhang, Yang Zhai, Hengjie Yuan

PMC · DOI: 10.3389/fcimb.2024.1497563 · Frontiers in Cellular and Infection Microbiology · 2025-02-20

## TL;DR

Xingnao Jiutan tablets help reduce brain injury after stroke by improving gut bacteria and their metabolites.

## Contribution

This study reveals that XNJT alleviates cerebral ischemia/reperfusion injury by modulating gut microbiota and their metabolic pathways.

## Key findings

- XNJT improved neurological function and reduced brain infarction in mice.
- XNJT decreased pro-inflammatory cytokines like TNF, IL-6, and IL-1b.
- XNJT modulated gut microbiota and metabolites through specific metabolic pathways.

## Abstract

Xingnao Jiutan tablets (XNJT), a compound Chinese medicine, have been applied to the treatment of the sequelae of cerebral thrombosis or cerebral hemorrhage, transient cerebral ischemia, and central retinal vein obstruction, etc., but the underlying mechanisms are not yet clear. This research focused on examining the impact of XNJT for cerebral ischemia/reperfusion (MCAO/R) injury, utilizing gut microbiota and metabolomic studies.

The primary components of XNJT were identified through the application of the HPLC technique. We established a MCAO/ R model in mice and conducted behavioral evaluations, cerebral blood flow measurements, and TTC staining. We used ELISA, high-throughput 16S rDNA gene sequencing, and metabolomics techniques to detect inflammatory factors, microbial populations, and metabolites, respectively. Finally, we performed Spearman correlation analysis to investigate the relationships among gut microbiota and metabolites, comprehensively exploring the mechanisms of XNJT to alleviate cerebral ischemia-reperfusion injury.

We discovered that XNJT effectively enhanced neurological performance, alleviated cerebral infarction, diminished neuronal cell death, and increased cerebral blood flow. Moreover, XNJT downregulated the secretion of pro-inflammatory cytokines like TNF, IL-6, and IL-1b. Additionally, XNJT improved gut microbiota levels in MCAO/R mice, particularly Bacteroides, Firmicutes, Escherichia-Shigella, and Ligilactobacillus. Furthermore, XNJT primarily modulated differential metabolites in the gut through Glycerophospholipid, Linoleic acid, and Sphingolipid metabolism pathways. Spearman correlation analysis revealed significant associations among intestinal microbiota and various metabolites.

In summary, our findings suggest that XNJT can improve cerebral ischemia/reperfusion injury outcomes, reduce inflammatory responses, and regulate gut microbiota and differential metabolites. It’s possible that the potential mechanisms are connected to controlling gut microbiota and metabolism.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** cerebral thrombosis (MESH:D020767), retinal vein obstruction (MESH:D012173), MCAO/ R (MESH:C580424), cerebral ischemia/reperfusion injury (MESH:D015427), inflammatory (MESH:D007249), cerebral ischemia (MESH:D002545), cerebral infarction (MESH:D002544), cerebral hemorrhage (MESH:D002543)
- **Species:** Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bacteroides (genus) [taxon 816], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC11882549/full.md

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Source: https://tomesphere.com/paper/PMC11882549