Potential Molecular Mechanism of Probiotics in Alcoholic Liver Disease

Dhara Patel, Farhin Patel, M. Palash
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引用次数: 4

Abstract

Alcohol consumption and its abuse are significant prevalent cause for liver diseases and death worldwide. Increased bacterial endotoxin in the portal circulation, the plasma ratio of liver enzymes like alanine aminotransferase (ALT), aspartate aminotransferase (AST) and triglyceride implies the symbiotic relation between the gut and liver plays a key function in alcoholic liver disease (ALD). Consumption of alcohol leads to gut dysbiosis and informalities of the intestinal barrier, hyper gut permeability, oxidative stress, inflammation and adversely affect adipose tissue metabolism, and those are mainly recognized as major factors for progression of alcoholic liver disease. Alteration of gut microbiota is referred to as bacterial overgrowth which leads to the release of bacterial products to change in commercial/pathogenic microbiota equilibrium. Lipopolysaccharide (LPS) derived inflammatory signal renders inflammation in alcoholic liver disease. Increase in concentration of lipopolysaccharide leads to activation of toll-like receptor 4 (TLR4) and alteration in micro RNA (miRNA) expression at the transcription level. Activation of myeloid differentiation factor 88 (MyD88) pathways eventually produces pro inflammatory cytokine activation that is an important mediator of alcoholic liver disease. However, there is no effectual Food and Drug Administration (FDA) approved treatment for any stage of alcoholic liver disease. Thus, the potential therapeutic approach for alcoholic liver disease is restoration and alteration of gut microbiota. With the increasing importance of gut microbiota in the onset and occurrence of a variety of diseases, the potential use of probiotics in ALD is receiving more exploration and clinical attention. Probiotic administration is nontoxic, inexpensive and noninvasive strategy with minimal side effects compared to antibiotic therapy and surgery. Yet, there is no substantial evidence on the efficient molecular mechanism regarding mode of action of probiotics on ALD as therapeutics. This review summarizes the research done on gut liver-axis and potential mechanism of probiotic in alcoholic liver disease.
益生菌治疗酒精性肝病的潜在分子机制
酒精消费和滥用是世界范围内肝脏疾病和死亡的重要普遍原因。门静脉循环细菌内毒素升高,血浆中丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、甘油三酯等肝脏酶的比值提示肠道与肝脏的共生关系在酒精性肝病(ALD)中起关键作用。饮酒导致肠道生态失调和肠道屏障紊乱、肠道通透性过强、氧化应激、炎症以及对脂肪组织代谢产生不利影响,这些都是目前公认的酒精性肝病进展的主要因素。肠道微生物群的改变被称为细菌过度生长,导致细菌产物的释放,从而改变商业/致病微生物群的平衡。脂多糖(LPS)衍生的炎症信号导致酒精性肝病的炎症。脂多糖浓度的升高导致toll样受体4 (TLR4)的激活和转录水平上微RNA (miRNA)表达的改变。髓样分化因子88 (MyD88)途径的激活最终产生促炎细胞因子激活,这是酒精性肝病的重要介质。然而,目前还没有有效的食品和药物管理局(FDA)批准治疗任何阶段的酒精性肝病。因此,酒精性肝病的潜在治疗方法是恢复和改变肠道微生物群。随着肠道菌群在多种疾病的发病和发生中的作用越来越重要,益生菌在ALD中的潜在应用正受到越来越多的探索和临床关注。与抗生素治疗和手术相比,益生菌治疗是一种无毒、廉价、无创的策略,副作用最小。然而,益生菌作为治疗ALD的有效分子机制尚未得到充分的证据。本文就益生菌在酒精性肝病中的作用机制及肠道肝轴的研究进展作一综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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