# Erxian Decoction Ameliorates Myocardial Damage in Ovariectomized Rats by Regulating the Gut Microbiota and TMAO-Mediated NLRP3 Inflammatory Pathway

## TL;DR

Erxian Decoction improves heart health in menopause-like rats by changing gut bacteria and reducing inflammation linked to heart disease.

## Contribution

Erxian Decoction's novel cardiovascular benefits via gut microbiota and TMAO-mediated NLRP3 pathway modulation in ovariectomized rats are demonstrated.

## Key findings

- Erxian Decoction improved heart function and reduced inflammation in ovariectomized rats.
- The decoction altered gut microbiota composition and lowered TMAO and its precursor metabolites.
- Erxian Decoction reduced blood pressure and lipid levels in the rats.

## Abstract

Menopausal women face an increased risk of cardiovascular diseases (CVDs), and exploring effective therapeutic strategies from traditional Chinese medicine is of great clinical significance. Erxian decoction (EXD), a classic formula for alleviating menopausal symptoms, has potential cardiovascular protective effects, but its underlying mechanisms remain unclear. In this study, the effects of EXD on gut microbiota, TMAO levels, and inflammatory levels were evaluated in ovariectomized (OVX) rats, a well-established model of menopausal CVDs. EXD elevated serum E2 levels and improved both the cardiac systolic and diastolic functions in OVX rats. EXD decreased Firmicutes and Ruminococcaceae, increased Bacteroidota, Muribaculaceae and Escherichia-Shigella. EXD significantly decreased serum levels of TMAO and its precursor metabolites. Additionally, it attenuated myocardial expression of ROS, TXNIP, NLRP3, ASC, Caspase 1, IL-18, and IL-1β. EXD could reduce the levels of SBP and DBP, and reduce the serum levels of TC, TG and LDL-C. Spearman correlation analysis revealed positive associations between TMAO and blood pressure, as well as inflammatory factors and dyslipidemia. Collectively, EXD may ameliorate myocardial damage in OVX rats through modulation of the gut microbiota and suppression of the TMAO-mediated NLRP3 inflammasome pathway, demonstrating its potential therapeutic implications for cardiovascular disorders.