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补阳还五汤通过调节载脂蛋白 E 缺陷小鼠高脂饮食的肠道微生物群和代谢物来缓解动脉粥样硬化。

Buyang Huanwu Decoction Alleviates Atherosclerosis by Regulating gut Microbiome and Metabolites in Apolipoprotein E-deficient Mice fed with High-fat Diet.

机构信息

School of Preclinical Medicine, Zunyi Medical University, Zunyi, Guizhou Province, China.

School of Integrated Chinese and Western Medicine, Tianjin University of Traditional Chinese Medicine, Jinghai, Tianjin, China.

出版信息

J Physiol Investig. 2024 Mar 1;67(2):88-102. doi: 10.4103/ejpi.EJPI-D-23-00031. Epub 2024 Apr 30.

Abstract

The traditional Chinese herbal prescription Buyang Huanwu decoction (BHD), effectively treats atherosclerosis. However, the mechanism of BHD in atherosclerosis remains unclear. We aimed to determine whether BHD could alleviate atherosclerosis by altering the microbiome-associated metabolic changes in atherosclerotic mice. An atherosclerotic model was established in apolipoprotein E-deficient mice fed high-fat diet, and BHD was administered through gavage for 12 weeks at 8.4 g/kg/d and 16.8 g/kg/d. The atherosclerotic plaque size, composition, serum lipid profile, and inflammatory cytokines, were assessed. Mechanistically, metabolomic and microbiota profiles were analyzed by liquid chromatography-mass spectrometry and 16S rRNA gene sequencing, respectively. Furthermore, intestinal microbiota and atherosclerosis-related metabolic parameters were correlated using Spearman analysis. Atherosclerotic mice treated with BHD exhibited reduced plaque area, aortic lumen occlusion, and lipid accumulation in the aortic root. Nine perturbed serum metabolites were significantly restored along with the relative abundance of microbiota at the family and genus levels but not at the phylum level. Gut microbiome improvement was strongly negatively correlated with improved metabolite levels. BHD treatment effectively slows the progression of atherosclerosis by regulating altered intestinal microbiota and perturbed metabolites.

摘要

中药方剂补阳还五汤(BHD)可有效治疗动脉粥样硬化。然而,BHD 治疗动脉粥样硬化的机制尚不清楚。我们旨在确定 BHD 是否可以通过改变动脉粥样硬化小鼠与微生物组相关的代谢变化来缓解动脉粥样硬化。通过给予载脂蛋白 E 缺陷小鼠高脂饮食建立动脉粥样硬化模型,并通过灌胃给予 BHD 治疗 12 周,剂量分别为 8.4 g/kg/d 和 16.8 g/kg/d。评估了动脉粥样硬化斑块大小、组成、血清脂质谱和炎症细胞因子。通过液相色谱-质谱和 16S rRNA 基因测序分别分析代谢组学和微生物组学图谱。此外,使用 Spearman 分析对肠道微生物群和与动脉粥样硬化相关的代谢参数进行相关性分析。BHD 治疗的动脉粥样硬化小鼠斑块面积减小,主动脉腔闭塞,主动脉根部脂质堆积减少。与菌群水平相比,血清代谢物的相对丰度在科和属水平上显著恢复,而在门水平上没有显著恢复。肠道微生物群的改善与改善的代谢物水平呈强烈负相关。BHD 治疗通过调节改变的肠道微生物群和失调的代谢物有效减缓动脉粥样硬化的进展。

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