1996
DOI: 10.1007/978-1-4613-0381-7_2
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Metabolism and Biology of Tryptophan

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Cited by 18 publications
(14 citation statements)
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“…It is of theoretical interest that increased production of interferon-γ (IFN-γ), known to be the predominant cytokine produced by gluten-specific T-cells in active coeliac disease [29], can suppress serotonin function both directly and indirectly by enhancing tryptophan and serotonin turnover [30]. Increased IFN-γ [30] and, for instance, such events as a stress-related increase in liver tryptophan pyrrolase enzyme activity [23], may lead to lowered tryptophan levels by the enhanced tryptophan catabolism induced by increased activity of the kynurenine-niacin pathway [30-32], even without malabsorption.…”
Section: Discussionmentioning
confidence: 99%
“…It is of theoretical interest that increased production of interferon-γ (IFN-γ), known to be the predominant cytokine produced by gluten-specific T-cells in active coeliac disease [29], can suppress serotonin function both directly and indirectly by enhancing tryptophan and serotonin turnover [30]. Increased IFN-γ [30] and, for instance, such events as a stress-related increase in liver tryptophan pyrrolase enzyme activity [23], may lead to lowered tryptophan levels by the enhanced tryptophan catabolism induced by increased activity of the kynurenine-niacin pathway [30-32], even without malabsorption.…”
Section: Discussionmentioning
confidence: 99%
“…70 Interferon-c can suppress serotonin function both directly and indirectly by enhancing serotonin turnover. 71 Fourthly, immunological events can lead to local intestinal complications. In patients with type-2 RCD, clonal expansion of intraepithelial lymphocytes appears to be driven by IL-15 secreted by epithelial cells.…”
Section: Ongoing Mucosal Inflammation and Injurymentioning
confidence: 99%
“…1.13.1.2) and indoleamine 2,3‐dioxygenase (IDO; E.C.1.13.11.42) [11,13]. TDO is predominantly (or exclusively) located in the liver and has a very strict substrate specificity acting only on l ‐TRP, while IDO has a lower substrate specificity (it may open the indole ring not only of l ‐TRP but also of d ‐TRP, l ‐ or d ‐5OH‐TRP and 5HT) and is present in most mammalian cells including human blood mononuclear macrophages [14,15].…”
Section: Introductionmentioning
confidence: 99%
“…The enzyme may control the growth of parasites and act as an endogenous regulator of T‐cell proliferation [16–18]. Inflammatory cytokines, produced as a consequence of parasite, bacterial or viral infections, increase IDO activity and expression thus causing a reduction in TRP and an increase in kynurenine metabolites in blood and brain [11,14,19,20].…”
Section: Introductionmentioning
confidence: 99%