Gut dysbiosis correction contributes to the hepatoprotective effects ofThymus quinquecostatusCelak extract against alcohol through the gut–liver axis

失调 TLR4型 酒精性肝病 肠道菌群 免疫学 脂多糖 肝损伤 生物 医学 药理学 内科学 免疫系统 肝硬化
作者
Xin Yan,Yu Wang,Xueyang Ren,Xiaoyun Liu,Jiamu Ma,Ruolan Song,Xiuhuan Wang,Ying Dong,Axiang Yu,Qiqi Fan,Jing Wei,Gaimei She
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:12 (20): 10281-10290 被引量:16
标识
DOI:10.1039/d1fo01117k
摘要

Alcoholic liver disease (ALD) is a major health issue globally due to the consumption of alcoholic beverages. Thymus quinquecostatus Celak is a food additive and an edible herb that is widely used in Asia and possesses hepatoprotective activity, but the underlying mechanisms behind this protective activity are not completely understood. The purpose of this study was to investigate the hepatoprotective effects of Thymus quinquecostatus Celak extract (TQE) against ALD as well as the underlying mechanism based on gut microbiota and the gut-liver axis. TQE supplementation markedly alleviated chronic alcohol-induced liver injury in C57 mice. TQE also ameliorated gut barrier dysfunction induced by alcohol. Consequently, the activation of the lipopolysaccharide (LPS) translocation-mediated TLR4 pathway and the subsequent inflammatory response and ROS overproduction in the liver were suppressed. Meanwhile, alcohol-induced gut microbiota dysbiosis was also corrected by TQE. To further investigate the contribution of gut dysbiosis correction to the beneficial effects of TQE on ALD, a fecal microbiota transplantation study was conducted. TQE-manipulated gut microbiota transplantation markedly counteracted the alcohol-induced gut dysbiosis in the recipient mice. In parallel with gut dysbiosis correction, liver damage was partly ameliorated in the recipient mice. Gut barrier dysfunction, endotoxemia, TLR4 pathway induction as well as downstream inflammatory response and ROS overproduction were also partly suppressed due to gut dysbiosis correction in alcohol-fed recipient mice. In summary, these results suggest that gut dysbiosis correction contributes to the hepatoprotective effects of TQE against alcohol through the gut-liver axis.
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