Intestinal Dysbiosis, the Tryptophan Pathway and Nonalcoholic Steatohepatitis.

IF 4.1
International journal of tryptophan research : IJTR Pub Date : 2022-02-07 eCollection Date: 2022-01-01 DOI:10.1177/11786469211070533
Jiezhong Chen, Luis Vitetta, Jeremy D Henson, Sean Hall
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引用次数: 5

Abstract

Non-alcoholic fatty liver disease (NAFLD) progresses from simple steatosis to steatohepatitis (NASH), which may then progress to the development of cirrhosis and hepatocarcinoma. NASH is characterized by both steatosis and inflammation. Control of inflammation in NASH is a key step for the prevention of disease progression to severe sequalae. Intestinal dysbiosis has been recognized to be an important causal factor in the pathogenesis of NASH, involving both the accumulation of lipids and aggravation of inflammation. The effects of gut dysbiosis are mediated by adverse shifts of various intestinal commensal bacterial genera and their associated metabolites such as butyrate, tryptophan, and bile acids. In this review, we focus on the roles of tryptophan and its metabolites in NASH in association with intestinal dysbiosis and discuss possible therapeutic implications.

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肠道生态失调,色氨酸途径和非酒精性脂肪性肝炎。
非酒精性脂肪性肝病(NAFLD)可由单纯脂肪变性发展为脂肪性肝炎(NASH),继而发展为肝硬化和肝癌。NASH以脂肪变性和炎症为特征。控制NASH的炎症是预防疾病发展为严重后遗症的关键步骤。肠道生态失调已被认为是NASH发病的重要原因,包括脂质积累和炎症加重。肠道生态失调的影响是由各种肠道共生细菌属及其相关代谢物(如丁酸盐、色氨酸和胆汁酸)的不利变化介导的。在这篇综述中,我们重点关注色氨酸及其代谢物在与肠道生态失调相关的NASH中的作用,并讨论可能的治疗意义。
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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