Altered gut microbial profiles in drug-treated rats with alcoholic heart disease.

Siang Wei, Yan Feng, Ai Meng, Zhiwen Ding, Wenji Lin
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Abstract

Introduction. 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.Hypothesis. 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.Aim. 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.Methodology. We evaluated body weight, cardiac function, changes in gut morphology, and gut microbiota composition to assess the effects of SSYX and amiodarone on AHD.Results. 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.Conclusion. SSYX and amiodarone may have potential therapeutic options for AHD. Actinobacteria/Firmicutes ratio and the abundance of Christensenellaceae R7 group, norank_flachnospiraceae and Roseburia may serve as potential biomarkers for detecting alcoholic heart disease.

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酒精性心脏病大鼠用药后肠道微生物谱的改变
介绍。酒精滥用可导致严重的心脏损伤,导致酒精性心脏病(AHD)。在饮酒的情况下,心脏健康和肠道微生物群组成之间的相互作用尚不清楚。沈松养心胶囊和胺碘酮是治疗酒精性心脏病的常用药物,但其在酒精性心脏病中的微生物调控机制尚不清楚。探讨SSYX和胺碘酮对酒精所致AHD大鼠模型心脏损伤和肠道微生物群组成的影响。我们评估了体重、心功能、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。饮酒可显著降低体重并加重心脏纤维化。然而,SSYX可减轻纤维化并改善心功能。SSYX还能改善慢性酒精中毒引起的肠道形态学改变,激活ZO-1和occludin的表达,这两种蛋白在维持肠道屏障功能中起重要作用。AHD大鼠肠道菌群组成发生改变,放线菌丰度增加。SSYX和胺碘酮均影响肠道菌群组成,且两者的影响呈正相关。SSYX对酒精引起的心脏损伤起保护作用。改善心脏功能,改善肠道形态改变,改善肠道菌群组成。SSYX和胺碘酮可能是adhd的潜在治疗选择。放线菌/厚壁菌门比值以及Christensenellaceae R7组、norank_flachnospiraceae和Roseburia的丰度可能作为检测酒精性心脏病的潜在生物标志物。
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