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酒精相关性肝病中的关键信号通路:胆汁酸的作用。

Key Signaling in Alcohol-Associated Liver Disease: The Role of Bile Acids.

机构信息

Center for Clinical and Translational Research, Virginia Commonwealth University, Richmond, VA 23298, USA.

Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298, USA.

出版信息

Cells. 2022 Apr 18;11(8):1374. doi: 10.3390/cells11081374.

Abstract

Alcohol-associated liver disease (ALD) is a spectrum of diseases, the onset and progression of which are due to chronic alcohol use. ALD ranges, by increasing severity, from hepatic steatosis to alcoholic hepatitis (AH) and alcohol-associated cirrhosis (AC), and in some cases, can lead to the development of hepatocellular carcinoma (HCC). ALD continues to be a significant health burden and is now the main cause of liver transplantations in the United States. ALD leads to biological, microbial, physical, metabolic, and inflammatory changes in patients that vary depending on disease severity. ALD deaths have been increasing in recent years and are projected to continue to increase. Current treatment centers focus on abstinence and symptom management, with little in the way of resolving disease progression. Due to the metabolic disruption and gut dysbiosis in ALD, bile acid (BA) signaling and metabolism are also notably affected and play a prominent role in disease progression in ALD, as well as other liver disease states, such as non-alcoholic fatty liver disease (NAFLD). In this review, we summarize the recent advances in the understanding of the mechanisms by which alcohol consumption induces hepatic injury and the role of BA-mediated signaling in the pathogenesis of ALD.

摘要

酒精相关性肝病(ALD)是一系列疾病,其发病和进展是由于长期饮酒所致。ALD 从轻到重依次为肝脂肪变性、酒精性肝炎(AH)和酒精相关性肝硬化(AC),在某些情况下,可导致肝细胞癌(HCC)的发展。ALD 仍然是一个重大的健康负担,现在是美国肝移植的主要原因。ALD 导致患者的生物学、微生物学、物理、代谢和炎症发生变化,具体变化取决于疾病的严重程度。近年来,ALD 死亡率一直在上升,预计还会继续上升。目前的治疗中心侧重于戒酒和症状管理,很少能解决疾病进展问题。由于 ALD 中的代谢紊乱和肠道菌群失调,胆汁酸(BA)信号和代谢也受到显著影响,并在 ALD 以及其他肝病状态(如非酒精性脂肪性肝病(NAFLD))的疾病进展中发挥重要作用。在这篇综述中,我们总结了近年来对饮酒诱导肝损伤的机制以及 BA 介导的信号在 ALD 发病机制中的作用的理解的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6259/9031669/94ca8f4e0fe5/cells-11-01374-g002.jpg

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