Golden bifid treatment regulates gut microbiota and serum metabolites to improve myocardial dysfunction in cecal ligation and puncture-induced sepsis mice

被引:2
作者
Wu, Rui [1 ]
Xu, Junmei [1 ]
Zeng, Hua [1 ]
Fan, Yongmei [2 ]
Li, Hui [1 ]
Peng, Tian [1 ]
Xiao, Feng [1 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Anesthesiol, Changsha 410011, Peoples R China
[2] Cent South Univ, Xiangya Hosp 2, Dept Rehabil, Changsha 410011, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2024年 / 1870卷 / 03期
关键词
Sepsis; Myocardial dysfunction; Golden bifid; Gut microbiota; Serum metabolites; SEPTIC SHOCK; LYSOPHOSPHATIDYLCHOLINE; RECEPTOR;
D O I
10.1016/j.bbadis.2024.167049
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myocardial damage is a major consequence and a significant contributor to death in cases of sepsis, a severe infection characterized by a distinct inflammatory response and a potential threat to the patient's life. Recently, the effects of intestinal microbiota and serum metabolites on sepsis have garnered increasing attention. Herein, the effects of golden bifid treatment upon cecal ligation and puncture (CLP)-induced sepsis in mice as a model for myocardial dysfunction were explored. Our results demonstrated that golden bifid treatment partially improved myocardial dysfunction and apoptosis, cardiac inflammation and oxidative stress, and intestinal mucosal permeability and barrier dysfunction in CLP-induced sepsis mice. The intestinal microbiota diversity and abundance were also altered within sepsis mice and improved by golden bifid treatment. Mucispirillum schaedleri, Acinetobacter baumannii and Lactobacullus intestinalis were significantly correlated with heart damage markers, inflammatory factors, or oxidative stress indicators. Serum differential metabolite levels were also significantly correlated with these parameters. Altogether, golden bifid treatment might be an underlying approach for treating sepsis-induced myocardial dysfunction and highlight the underlying effect of intestinal microbiota and serum metabolites on the pathogenesis and treatment of sepsis-triggered myocardial dysfunction.
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页数:14
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