AI Article Synopsis

  • Trimethylamine N-oxide (TMAO) is a gut microbiome-derived metabolite linked to various diseases like atherosclerosis, hypertension, diabetes, and hyperlipidemia due to its role in causing endothelial dysfunction.
  • The mechanisms by which TMAO induces this dysfunction include inflammation, oxidative stress, activation of foam cells, upregulation of cytokines, increased reactive oxygen species, platelet hyperreactivity, and reduced vascular tone.
  • The review explores TMAO's impact on endothelial dysfunction in cardio-metabolic diseases and discusses potential therapeutic strategies to address these issues.

Article Abstract

Trimethylamine N-oxide (TMAO) is a biologically active gut microbiome-derived dietary metabolite. Recent studies have shown that high circulating plasma TMAO levels are closely associated with diseases such as atherosclerosis and hypertension, and metabolic disorders such as diabetes and hyperlipidemia, contributing to endothelial dysfunction. There is a growing interest to understand the mechanisms underlying TMAO-induced endothelial dysfunction in cardio-metabolic diseases. Endothelial dysfunction mediated by TMAO is mainly driven by inflammation and oxidative stress, which includes: (1) activation of foam cells; (2) upregulation of cytokines and adhesion molecules; (3) increased production of reactive oxygen species (ROS); (4) platelet hyperreactivity; and (5) reduced vascular tone. In this review, we summarize the potential roles of TMAO in inducing endothelial dysfunction and the mechanisms leading to the pathogenesis and progression of associated disease conditions. We also discuss the potential therapeutic strategies for the treatment of TMAO-induced endothelial dysfunction in cardio-metabolic diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142468PMC
http://dx.doi.org/10.3390/ph16040504DOI Listing

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