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Tryptophan-derived serotonin-kynurenine balance in immune activation and intestinal inflammation.

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TLDR
The role of 5-HT and kynurenine in immune regulation and intestinal inflammation was investigated in this article, where the current knowledge of the relationship and interactions between 5-HHT and KN was analyzed.
Abstract
Endogenous tryptophan metabolism pathways lead to the production of serotonin (5-hydroxytryptamine; 5-HT), kynurenine, and several downstream metabolites which are involved in a multitude of immunological functions in both health and disease states. Ingested tryptophan is largely shunted to the kynurenine pathway (95%) while only minor portions (1%-2%) are sequestered for 5-HT production. Though often associated with the functioning of the central nervous system, significant production of 5-HT, kynurenine and their downstream metabolites takes place within the gut. Accumulating evidence suggests that these metabolites have essential roles in regulating immune cell function, intestinal inflammation, as well as in altering the production and suppression of inflammatory cytokines. In addition, both 5-HT and kynurenine have a considerable influence on gut microbiota suggesting that these metabolites impact host physiology both directly and indirectly via compositional changes. It is also now evident that complex interactions exist between the two pathways to maintain gut homeostasis. Alterations in 5-HT and kynurenine are implicated in the pathogenesis of many gastrointestinal dysfunctions, including inflammatory bowel disease. Thus, these pathways present numerous potential therapeutic targets, manipulation of which may aid those suffering from gastrointestinal disorders. This review aims to update both the role of 5-HT and kynurenine in immune regulation and intestinal inflammation, and analyze the current knowledge of the relationship and interactions between 5-HT and kynurenine pathways.

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Interactions between Tryptophan Metabolism, the Gut Microbiome and the Immune System as Potential Drivers of Non-Alcoholic Fatty Liver Disease (NAFLD) and Metabolic Diseases

TL;DR: This narrative review summarizes the interactions between tryptophan metabolism, the gut microbiome and the immune system as potential drivers of cardiometabolic diseases in NAFLD.
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Macrophage immunometabolism in inflammatory bowel diseases: From pathogenesis to therapy.

TL;DR: In this article , metabolic alterations underlie intestinal macrophage phenotype and function during IBD, and how microenvironmental cues trigger their metabolic reprogramming processes, and also summarized potential therapeutic approaches for IBD by manipulating cellular metabolism of macrophages.
Journal ArticleDOI

An Emerging Cross-Species Marker for Organismal Health: Tryptophan-Kynurenine Pathway

TL;DR: Key pathways affecting Trp-Kyn metabolism in vertebrates are identified and consequences of altered tryptophan metabolism in mammals, birds, amphibians, and fish are highlighted to highlight gaps in the current state of knowledge and postulate that the kynurenine to tryPTophan ratio can be used as a novel biomarker for assessing organismal and ecosystem health.
Journal ArticleDOI

Tryptophan regulates Drosophila zinc stores

TL;DR: The discovery that tryptophan metabolites 3-hydroxykynurenine and xanthurenic acid are major zinc-binding ligands in insect cells establishes the kynurenines pathway as a regulator of systemic zinc homeostasis.
Journal ArticleDOI

Gut-derived serotonin and its emerging roles in immune function, inflammation, metabolism and the gut–brain axis

TL;DR: The role of peripheral 5-HT in the regulation of various physiological and pathophysiological conditions opens up new targets for researchers to explore and for clinicians to treat and manage different diseases associated with the altered 5HT signalling as discussed by the authors .
References
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Journal ArticleDOI

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Indigenous Bacteria from the Gut Microbiota Regulate Host Serotonin Biosynthesis

TL;DR: It is demonstrated that Indigenous spore-forming bacteria from the mouse and human microbiota promote 5-HT biosynthesis from colonic enterochromaffin cells (ECs), which supply 5- HT to the mucosa, lumen, and circulating platelets and elevating luminal concentrations of particular microbial metabolites increases colonic and blood5-HT in germ-free mice.
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The global burden of IBD: from 2015 to 2025

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The Expanded Biology of Serotonin

TL;DR: New work suggests that serotonin may regulate some processes, including platelet aggregation, by receptor-independent, transglutaminase-dependent covalent linkage to cellular proteins.
Journal ArticleDOI

Inhibition of t cell proliferation by macrophage tryptophan catabolism

TL;DR: It is shown that monocytes that have differentiated under the influence of macrophage colony-stimulating factor acquire the ability to suppress T cell proliferation in vitro via rapid and selective degradation of tryptophan by IDO.
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