Tomasova Lenka, Grman Marian, Ondrias Karol, Ufnal Marcin
Institute of Clinical and Translational Research, Biomedical Research Center, Slovak Academy of Sciences, Dubravska cesta 9, 845 05, Bratislava, Slovak Republic.
Department of Experimental Physiology and Pathophysiology, Laboratory of Centre for Preclinical Research, Medical University of Warsaw, 02-091, Warsaw, Poland.
Nutr Metab (Lond). 2021 Jul 15;18(1):72. doi: 10.1186/s12986-021-00598-5.
Recent research demonstrates a reciprocal relationship between gut microbiota-derived metabolites and the host in controlling the energy homeostasis in mammals. On the one hand, to thrive, gut bacteria exploit nutrients digested by the host. On the other hand, the host utilizes numerous products of gut bacteria metabolism as a substrate for ATP production in the colon. Finally, bacterial metabolites seep from the gut into the bloodstream and interfere with the host's cellular bioenergetics machinery. Notably, there is an association between alterations in microbiota composition and the development of metabolic diseases and their cardiovascular complications. Some metabolites, like short-chain fatty acids and trimethylamine, are considered markers of cardiometabolic health. Others, like hydrogen sulfide and nitrite, demonstrate antihypertensive properties. Scientific databases were searched for pre-clinical and clinical studies to summarize current knowledge on the role of gut microbiota metabolites in the regulation of mammalian bioenergetics and discuss their potential involvement in the development of cardiometabolic disorders. Overall, the available data demonstrates that gut bacteria products affect physiological and pathological processes controlling energy and vascular homeostasis. Thus, the modulation of microbiota-derived metabolites may represent a new approach for treating obesity, hypertension and type 2 diabetes.
最近的研究表明,肠道微生物群衍生的代谢产物与宿主之间存在相互关系,可控制哺乳动物的能量平衡。一方面,为了生存,肠道细菌利用宿主消化的营养物质。另一方面,宿主利用肠道细菌代谢的众多产物作为结肠中ATP产生的底物。最后,细菌代谢产物从肠道渗入血液,干扰宿主的细胞生物能量学机制。值得注意的是,微生物群组成的改变与代谢性疾病及其心血管并发症的发生之间存在关联。一些代谢产物,如短链脂肪酸和三甲胺,被认为是心脏代谢健康的标志物。其他代谢产物,如硫化氢和亚硝酸盐,具有降压特性。检索科学数据库以查找临床前和临床研究,以总结当前关于肠道微生物群代谢产物在调节哺乳动物生物能量学中的作用的知识,并讨论它们在心脏代谢紊乱发展中的潜在参与。总体而言,现有数据表明肠道细菌产物会影响控制能量和血管稳态的生理和病理过程。因此,调节微生物群衍生的代谢产物可能代表一种治疗肥胖、高血压和2型糖尿病的新方法。