Electroacupuncture interventions alleviates myocardial ischemia reperfusion injury through regulating gut microbiota in rats

心肌保护 医学 电针 再灌注损伤 缺血 内科学 H&E染色 肠道菌群 内分泌学 免疫学 病理 免疫组织化学 针灸科 替代医学
作者
Hua Bai,Renjun Gu,Li-Yao Chen,Yi Qian,Meiling Yu,Sen-Lei Xu,Xuefeng Xia,Yuchen Liu,Hongru Zhang,Yi-Huang Gu,Sheng-Feng Lu
出处
期刊:Microvascular Research [Elsevier BV]
卷期号:138: 104235-104235 被引量:31
标识
DOI:10.1016/j.mvr.2021.104235
摘要

Electroacupuncture (EA) intervention has a remarkable cardioprotection against myocardial ischemia reperfusion injury (MIRI). Recently, it has been suggested that the gut microbiota plays an important role in regulating the progression and prognosis of MIRI. The purpose of this study was to illustrate the relationship between gut microbiota and cardioprotection of EA on MIRI. We conducted a MIRI model by ligating the left anterior descending coronary artery for 30 min followed by reperfusion in male Sprague Dawley rats, which then received 7 days of EA intervention. Echocardiography was employed to evaluate left ventricular function. Fecal samples were collected for microbial analysis by 16S rDNA high-throughput sequencing. Blood samples and myocardium were collected for inflammatory cytokine detection by enzyme linked immunosorbent assay (ELISA) and Western blot. Hematoxylin & eosin (HE) staining and immunofluorescence of ileum tissue were performed for intestinal damage evaluation. After 7 days of EA intervention, the left ventricular function was improved with significantly increased ejection fraction and fractional shortening. Furthermore, we found that EA intervention reversed the changed gut microbiota induced by MIRI, including Clostridiales, RF39, S24-7, Desulfovibrio, and Allobaculum, improved the impaired gut barrier, reduced the production and circulation of lipopolysaccharide (LPS), inhibited the level of interleukin 6 (IL-6) and interleukin 12 (IL-12) in periphery and decreased the expression of Toll like receptor 4 (TLR4) and IL-6 in myocardium. EA intervention could improve the impaired gut mucosal barrier and reduce the production and circulation of LPS after MIRI through regulating gut microbiota, thus inhibiting the circulation and myocardium inflammation and finally exerted the cardioprotective effect.
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