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Cited by 361

The DOI matches its Crossref record; 195 of the 195 references it cites were found in a registry or an index.

Tryptophan-kynurenine pathway is dysregulated in inflammation and immune activation

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Zou, Ming-Hui·2015·Frontiers in Bioscience

Abstract

The kynurenine (Kyn) pathway is the major route for tryptophan (Trp) metabolism, and it contributes to several fundamental biological processes. Trp is constitutively oxidized by tryptophan 2, 3-dioxygenase in liver cells. In other cell types, it is catalyzed by an alternative inducible indoleamine-pyrrole 2, 3-dioxygenase (IDO) under certain pathophysiological conditions, which consequently increases the formation of Kyn metabolites. IDO is up-regulated in response to inflammatory conditions as a novel marker of immune activation in early atherosclerosis. Besides, IDO and the IDO-related pathway are important mediators of the immunoinflammatory responses in advanced atherosclerosis. In particular, Kyn, 3-hydroxykynurenine, and quinolinic acid are positively associated with inflammation, oxidative stress (SOX), endothelial dysfunction, and carotid artery intima-media thickness values in end-stage renal disease patients. Moreover, IDO is a potential novel contributor to vessel relaxation and metabolism in systemic infections, which is also activated in acute severe heart attacks. The Kyn pathway plays a key role in the increased prevalence of cardiovascular disease by regulating inflammation, SOX, and immune activation.

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Metadata

Authors
Zou, M.-H.
Venue
Frontiers in Bioscience
Publisher
IMR Press
Published
2015
Volume
20
Issue
7
Pages
1116-1143
ISSN
  • 1093-4715 (ISSN-L)
  • 1093-9946
OpenAlex
W2471827535
Cited by
361
References
195
FWCI
4.04
Type
journal article
Language
en
Open access
bronze

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Zou, M.-H. (2015). Tryptophan-kynurenine pathway is dysregulated in inflammation and immune activation. Frontiers in Bioscience. https://doi.org/10.2741/4363

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