Kim Myungsuk, Huda Md Nazmul, Bennett Brian J
Obesity and Metabolism Research Unit, USDA, ARS, Western Human Nutrition Research Center, Davis, CA, USA.
Department of Nutrition, University of California Davis, Davis, CA, USA.
Cardiovasc Res. 2022 Jan 29;118(2):399-412. doi: 10.1093/cvr/cvab030.
The discovery that gut-microbiota plays a profound role in human health has opened a new avenue of basic and clinical research. Application of ecological approaches where the bacterial 16S rRNA gene is queried has provided a number of candidate bacteria associated with coronary artery disease and hypertension. We examine the associations between gut microbiota and a variety of cardiovascular disease (CVD) including atherosclerosis, coronary artery disease, and blood pressure. These approaches are associative in nature and there is now increasing interest in identifying the mechanisms underlying these associations. We discuss three potential mechanisms including: gut permeability and endotoxemia, increased immune system activation, and microbial derived metabolites. In addition to discussing these potential mechanisms we highlight current studies manipulating the gut microbiota or microbial metabolites to move beyond sequence-based association studies. The goal of these mechanistic studies is to determine the mode of action by which the gut microbiota may affect disease susceptibility and severity. Importantly, the gut microbiota appears to have a significant effect on host metabolism and CVD by producing metabolites entering the host circulatory system such as short-chain fatty acids and trimethylamine N-Oxide. Therefore, the intersection of metabolomics and microbiota research may yield novel targets to reduce disease susceptibility. Finally, we discuss approaches to demonstrate causality such as specific diet changes, inhibition of microbial pathways, and fecal microbiota transplant.
肠道微生物群在人类健康中发挥着深远作用这一发现,开辟了基础和临床研究的新途径。应用查询细菌16S rRNA基因的生态学方法,已发现了一些与冠状动脉疾病和高血压相关的候选细菌。我们研究肠道微生物群与包括动脉粥样硬化、冠状动脉疾病和血压在内的多种心血管疾病(CVD)之间的关联。这些方法本质上是关联性的,目前人们越来越有兴趣确定这些关联背后的机制。我们讨论三种潜在机制,包括:肠道通透性和内毒素血症、免疫系统激活增加以及微生物衍生代谢产物。除了讨论这些潜在机制外,我们还重点介绍了当前操纵肠道微生物群或微生物代谢产物以超越基于序列的关联研究的研究。这些机制研究的目标是确定肠道微生物群可能影响疾病易感性和严重程度的作用方式。重要的是,肠道微生物群似乎通过产生进入宿主循环系统的代谢产物,如短链脂肪酸和氧化三甲胺,对宿主代谢和心血管疾病产生重大影响。因此,代谢组学与微生物群研究的交叉可能会产生降低疾病易感性的新靶点。最后,我们讨论证明因果关系的方法,如特定饮食改变、微生物途径抑制和粪便微生物群移植。