The tryptophan-kynurenine pathway in cardiovascular diseases: mechanistic insights and therapeutic opportunities
Wei Chen, Min Shui, Zhen Wei, Weiyan Gao, Xin Liu, Qian Lei

TL;DR
This review explores how the tryptophan-kynurenine pathway contributes to cardiovascular diseases and highlights its potential for new diagnostics and treatments.
Contribution
The paper systematically reviews the role of the kynurenine pathway in CVDs and its potential as a therapeutic target.
Findings
Dysregulated kynurenine pathway metabolites are linked to heart failure, atherosclerosis, and hypertension.
KP metabolites influence immune activation, inflammation, and endothelial dysfunction in CVDs.
Metabolomics and AI could enhance CVD diagnosis and therapeutic development.
Abstract
Cardiovascular diseases (CVDs) are the leading cause of death worldwide, making them crucial to further explore their mechanisms. Beyond traditional risk factors, disturbances in tryptophan metabolism, particularly the imbalance in the kynurenine pathway (KP) which accounts for over 95% of metabolic flux—have garnered significant attention in cardiovascular research. In the human body, tryptophan is primarily metabolized through the KP. This process is catalyzed by key enzymes, indoleamine 2,3-dioxygenase and tryptophan 2,3-dioxygenase, which convert tryptophan into kynurenine and further downstream metabolites such as kynurenic acid and 3-hydroxykynurenine. Studies have shown that levels of multiple key metabolites in KP are dysregulated in patients with CVDs, and by participating in processes such as immune activation, inflammatory responses, reactive oxygen species production, and…
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Taxonomy
TopicsTryptophan and brain disorders · Cardiac Health and Mental Health · Inflammasome and immune disorders
