Department of Pharmaceutical Sciences and Technology, Maharaja Ranjit Singh Punjab Technical University, Bathinda, Punjab-151001, India.
Amity Institute of Pharmacy, Amity University, Noida, Uttar Pradesh-201303, India.
Endocr Metab Immune Disord Drug Targets. 2022;22(14):1344-1356. doi: 10.2174/1871530322666220624161712.
The gut microbiome consists of trillions of bacteria and other microbes whose metabolic activities and interactions with the immune system go beyond the gut itself. We are all aware that bacteria and other microorganisms have a significant impact on our health. Also, the health of the bacteria directly reflects the health status of the body where they reside. Eventually, alterations in the microbiome at different sites of a body are associated with many different diseases such as obesity, IBD, malnutrition, CVD, etc. Microbiota directly or indirectly affects the heart with the formation of plaques in the blood vessels, and cell walls become prone to lesion development. This ultimately leads to heightening the overall inflammatory status via increased bacterial translocation. Metabolites derived from the gut microbial metabolism of choline, phosphatidylcholine, and L-carnitine directly contribute to CVD pathology. These dietary nutrients have trimethylamine (TMA) moiety, which participates in the development of atherosclerotic heart disease. The objective of this review was to examine various metabolic pathways regulated by the gut microbiome that appear to alter heart function and lead to the development and progression of cardiovascular diseases, as well as how to target the gut microbiome for a healthier heart. In this review, we also discussed various clinical drugs having crosstalk between microbiota and heart and clinical trials for the gut-heart microbiome.
肠道微生物组由数万亿细菌和其他微生物组成,它们的代谢活动和与免疫系统的相互作用超出了肠道本身。我们都知道细菌和其他微生物对我们的健康有重大影响。此外,细菌的健康状况直接反映了它们所居住的身体的健康状况。最终,身体不同部位的微生物组的改变与许多不同的疾病有关,如肥胖、IBD、营养不良、CVD 等。微生物群直接或间接影响心脏,导致血管中斑块的形成,使细胞壁更容易发生病变。这最终通过增加细菌易位导致整体炎症状态的加剧。源自肠道微生物对胆碱、磷脂酰胆碱和左旋肉碱的代谢的代谢物直接导致 CVD 病理。这些膳食营养素含有三甲胺(TMA)部分,参与动脉粥样硬化性心脏病的发展。本综述的目的是研究肠道微生物组调节的各种代谢途径,这些途径似乎改变了心脏功能,导致心血管疾病的发展和进展,以及如何针对肠道微生物组来促进心脏健康。在这篇综述中,我们还讨论了微生物群和心脏之间存在相互作用的各种临床药物以及肠道-心脏微生物群的临床试验。