Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX 77204, USA.
Department of Pharmaceutical Sciences, Irma Lerma College of Pharmacy, Texas A&M University, Kingsville, TX 78363, USA.
Int J Mol Sci. 2024 Sep 23;25(18):10208. doi: 10.3390/ijms251810208.
Cardiovascular diseases (CVDs) are the leading cause of premature morbidity and mortality globally. The identification of novel risk factors contributing to CVD onset and progression has enabled an improved understanding of CVD pathophysiology. In addition to the conventional risk factors like high blood pressure, diabetes, obesity and smoking, the role of gut microbiome and intestinal microbe-derived metabolites in maintaining cardiovascular health has gained recent attention in the field of CVD pathophysiology. The human gastrointestinal tract caters to a highly diverse spectrum of microbes recognized as the gut microbiota, which are central to several physiologically significant cascades such as metabolism, nutrient absorption, and energy balance. The manipulation of the gut microbial subtleties potentially contributes to CVD, inflammation, neurodegeneration, obesity, and diabetic onset. The existing paradigm of studies suggests that the disruption of the gut microbial dynamics contributes towards CVD incidence. However, the exact mechanistic understanding of such a correlation from a signaling perspective remains elusive. This review has focused upon an in-depth characterization of gut microbial metabolites and their role in varied pathophysiological conditions, and highlights the potential molecular and signaling mechanisms governing the gut microbial metabolites in CVDs. In addition, it summarizes the existing courses of therapy in modulating the gut microbiome and its metabolites, limitations and scientific gaps in our current understanding, as well as future directions of studies involving the modulation of the gut microbiome and its metabolites, which can be undertaken to develop CVD-associated treatment options. Clarity in the understanding of the molecular interaction(s) and associations governing the gut microbiome and CVD shall potentially enable the development of novel druggable targets to ameliorate CVD in the years to come.
心血管疾病(CVDs)是全球范围内导致过早发病和死亡的主要原因。识别导致 CVD 发病和进展的新风险因素,使我们能够更好地了解 CVD 的病理生理学。除了高血压、糖尿病、肥胖和吸烟等传统危险因素外,肠道微生物组和肠道微生物衍生代谢物在维持心血管健康方面的作用在 CVD 病理生理学领域引起了人们的关注。人类胃肠道容纳了高度多样化的微生物,这些微生物被认为是肠道微生物群,它们是代谢、营养吸收和能量平衡等几个生理重要级联反应的核心。肠道微生物细微变化的操纵可能会导致 CVD、炎症、神经退行性变、肥胖和糖尿病的发生。现有研究范式表明,肠道微生物动态的破坏与 CVD 的发生有关。然而,从信号角度来看,这种相关性的确切机制理解仍然难以捉摸。本综述重点介绍了肠道微生物代谢物的深入特征及其在各种病理生理条件下的作用,并强调了控制 CVD 中肠道微生物代谢物的潜在分子和信号机制。此外,它总结了调节肠道微生物组及其代谢物的现有治疗方法、我们目前理解中的局限性和科学空白,以及未来涉及调节肠道微生物组及其代谢物的研究方向,这些研究可以用来开发与 CVD 相关的治疗选择。对控制肠道微生物组和 CVD 的分子相互作用(和关联)的理解的明晰化,可能会使我们在未来几年内开发出改善 CVD 的新型可药物靶点。
Protein Cell. 2018-5-3
Circ Res. 2020-7-31
Can J Microbiol. 2021-2
Curr Opin Cardiol. 2020-5
Biomedicines. 2025-5-25
J Clin Med. 2025-3-29
Front Pharmacol. 2025-1-7
Nat Cardiovasc Res. 2023-4
Am J Physiol Heart Circ Physiol. 2023-12-1
N Engl J Med. 2023-10-5
Cells. 2023-4-14