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乌药乙醇提取物通过肠道微生物群调节胆汁酸代谢减轻饮食诱导的高脂血症。

Linderae Radix Ethanol Extract Alleviates Diet-Induced Hyperlipidemia by Regulating Bile Acid Metabolism Through gut Microbiota.

作者信息

Jiang Tao, Xu Chuyun, Liu Huifang, Liu Muyi, Wang Minmin, Jiang Jiarui, Zhang Guangji, Yang Chuqi, Huang Jianbo, Lou Zhaohuan

机构信息

School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Front Pharmacol. 2021 Feb 17;12:627920. doi: 10.3389/fphar.2021.627920. eCollection 2021.

Abstract

Hyperlipidemia is a common metabolic disorder and regarded as one of the main risk factors for cardiovascular disease. The gut microbiota has been identified as a potential contributor to hyperlipidemia as it can greatly regulate bile acid metabolism. Linderae radix is a natural medicine widely used in the treatment of a variety of diseases and is also a common drug for hyperlipidemia. Recently, the lipid-lowering effect of Linderae radix are receiving increasing attention but the underlying mechanism remains unknown. The study aimed to investigate the effects of Linderae radix ethanol extract (LREE) on gut microbiota in rats with hyperlipidemia syndrome. We established a hyperlipidemia rat model using a high-fat diet and used LREE as the intervention. Blood lipid levels and pathological examination were measured to assess the effects of LREE on hyperlipidemia. The gut microbiota was determined by 16s rDNA sequencing and the bile acid metabolism-related proteins were detected by western blot to discover the underlying correlations. The results show that LREE lowered TC, TG, and LDL levels effectively, and it also alleviated liver injury by reducing ALT and AST activity. Meanwhile, LREE improved gut microbiota disturbance caused by HFD via increasing intestinal microbiota diversity and changing the abundance of the Firmicutes, Bacteroidetes, and Actinobacteria. In addition, LREE can increase bile acid reabsorption and promote fecal excretion through farnesoid X receptor (FXR), apical sodium-dependent bile acid transporter (ASBT), organic solute transporter alpha (OST-α), and cytochrome P450 family 7 Subfamily A Member 1 (CYP7A1) thus restoring abnormal bile acid metabolism caused by hyperlipidemia.

摘要

高脂血症是一种常见的代谢紊乱疾病,被视为心血管疾病的主要危险因素之一。肠道微生物群已被确定为高脂血症的一个潜在促成因素,因为它可以极大地调节胆汁酸代谢。乌药是一种广泛用于治疗多种疾病的天然药物,也是治疗高脂血症的常用药物。近年来,乌药的降血脂作用受到越来越多的关注,但其潜在机制仍不清楚。本研究旨在探讨乌药乙醇提取物(LREE)对高脂血症综合征大鼠肠道微生物群的影响。我们使用高脂饮食建立了高脂血症大鼠模型,并使用LREE作为干预措施。测量血脂水平和进行病理检查以评估LREE对高脂血症的影响。通过16s rDNA测序确定肠道微生物群,并通过蛋白质免疫印迹法检测胆汁酸代谢相关蛋白,以发现潜在的相关性。结果表明,LREE有效降低了TC、TG和LDL水平,还通过降低ALT和AST活性减轻了肝损伤。同时,LREE通过增加肠道微生物群多样性和改变厚壁菌门、拟杆菌门和放线菌门的丰度,改善了由高脂饮食引起的肠道微生物群紊乱。此外,LREE可以通过法尼酯X受体(FXR)、顶端钠依赖性胆汁酸转运蛋白(ASBT)、有机溶质转运蛋白α(OST-α)和细胞色素P450家族7亚家族A成员1(CYP7A1)增加胆汁酸重吸收并促进粪便排泄,从而恢复高脂血症引起的异常胆汁酸代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6029/7925880/102ca4b41d8e/fphar-12-627920-g001.jpg

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