Wei Siang, Feng Yan, Meng Ai, Ding Zhiwen, Lin Wenji
College of Life and Science, Shanxi Agricultural University, Shanxi 030801, PR China.
Beijing View Solid Biotech. Co., Ltd, Beijing 102200, PR China.
J Med Microbiol. 2025 Jan;74(1). doi: 10.1099/jmm.0.001930.
Alcohol abuse can lead to significant cardiac injury, resulting in Alcoholic heart disease (AHD). The interplay between cardiac health and gut microbiota composition in the context of alcohol consumption is not well understood. Shen Song Yang Xin (SSYX) capsule and amiodarone are common drugs used to treat alcoholic heart disease, but little is known about their microbial regulatory mechanisms in alcoholic heart disease. To investigate the effects of SSYX and amiodarone on cardiac injury and gut microbiota composition in a rat model of AHD induced by alcohol consumption. We evaluated body weight, cardiac function, changes in gut morphology, and gut microbiota composition to assess the effects of SSYX and amiodarone on AHD. Alcohol consumption significantly reduced body weight and aggravated cardiac fibrosis. However, SSYX attenuated fibrosis and improved cardiac function. SSYX also improved intestinal morphological changes caused by chronic alcoholism and activated the expression of ZO-1 and occludin, which are important in maintaining intestinal barrier function. The gut microbiota composition was altered in rats with AHD, with an increase in Actinobacteria abundance. Both SSYX and amiodarone affected the gut microbiota composition, and their effects were positively correlated. SSYX plays a protective role against heart injury caused by alcohol consumption. It improves cardiac function, intestinal morphological changes and gut microbiota composition. SSYX and amiodarone may have potential therapeutic options for AHD. Actinobacteria/Firmicutes ratio and the abundance of , and may serve as potential biomarkers for detecting alcoholic heart disease.
酒精滥用可导致严重的心脏损伤,引发酒精性心脏病(AHD)。在饮酒背景下,心脏健康与肠道微生物群组成之间的相互作用尚不清楚。参松养心胶囊(SSYX)和胺碘酮是治疗酒精性心脏病的常用药物,但它们在酒精性心脏病中的微生物调节机制鲜为人知。为了研究SSYX和胺碘酮对酒精摄入诱导的AHD大鼠模型中心脏损伤和肠道微生物群组成的影响。我们评估了体重、心脏功能、肠道形态变化和肠道微生物群组成,以评估SSYX和胺碘酮对AHD的影响。饮酒显著降低体重并加重心脏纤维化。然而,SSYX减轻了纤维化并改善了心脏功能。SSYX还改善了慢性酒精中毒引起的肠道形态变化,并激活了ZO-1和闭合蛋白的表达,这对维持肠道屏障功能很重要。AHD大鼠的肠道微生物群组成发生了改变,放线菌丰度增加。SSYX和胺碘酮都影响肠道微生物群组成,且它们的作用呈正相关。SSYX对饮酒引起的心脏损伤起保护作用。它改善心脏功能、肠道形态变化和肠道微生物群组成。SSYX和胺碘酮可能是治疗AHD的潜在选择。放线菌/厚壁菌门比率以及 、 和 的丰度可能作为检测酒精性心脏病的潜在生物标志物。