Literature DB >> 12814390

Immune activation and degradation of tryptophan in coronary heart disease.

B Wirleitner1, V Rudzite, G Neurauter, C Murr, U Kalnins, A Erglis, K Trusinskis, D Fuchs.   

Abstract

BACKGROUND: Inflammation and immune activation appear to be important in the pathogenesis of coronary heart disease (CHD). Cytokine interferon-gamma, which is released during cell-mediated immune responses, induces indoleamine (2,3)-dioxygenase (IDO), an enzyme degrading tryptophan to kynurenine. Therefore, immune stimulation is commonly associated with an increased kynurenine to tryptophan ratio (kyn trp-1) indicative for activated indoleamine (2,3)-dioxygenase and a measurable decline of tryptophan.
METHODS: Blood concentrations of kynurenine and free tryptophan and the kynurenine to tryptophan ratio were examined in 35 patients with coronary heart disease verified by coronary angiography and compared with healthy controls. Patients were observed before percutaneous transluminal coronary angioplasty (21 patients: one with artery disease, nine with 2- or 3-artery disease, and five with restenosis). RESULTS AND
CONCLUSIONS: Decreased tryptophan concentrations were found in a significant proportion of coronary heart disease patients and coincided with increased kyn trp-1 and also with increased neopterin concentrations, indicating an activated cellular immune response. We conclude that in coronary heart disease immune activation is associated with an increased rate of tryptophan degradation and thereby lowered tryptophan levels. Results may provide a basis for a better understanding of the pathogenesis of mood disturbances and depression in coronary heart disease patients.

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Year:  2003        PMID: 12814390     DOI: 10.1046/j.1365-2362.2003.01186.x

Source DB:  PubMed          Journal:  Eur J Clin Invest        ISSN: 0014-2972            Impact factor:   4.686


  46 in total

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Review 2.  Kynurenines and intestinal neurotransmission: the role of N-methyl-D-aspartate receptors.

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Review 3.  Disturbed tryptophan metabolism in cardiovascular disease.

Authors:  H Mangge; I Stelzer; E Z Reininghaus; D Weghuber; T T Postolache; D Fuchs
Journal:  Curr Med Chem       Date:  2014-06       Impact factor: 4.530

4.  Indoleamine 2,3-dioxygenase-1 is protective in atherosclerosis and its metabolites provide new opportunities for drug development.

Authors:  Jennifer E Cole; Nagore Astola; Adam P Cribbs; Michael E Goddard; Inhye Park; Patricia Green; Alun H Davies; Richard O Williams; Marc Feldmann; Claudia Monaco
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5.  Interferon-gamma-inducible kynurenines/pteridines inflammation cascade: implications for aging and aging-associated psychiatric and medical disorders.

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6.  Kynurenine pathway metabolites in humans: disease and healthy States.

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Journal:  Int J Tryptophan Res       Date:  2009-01-08

7.  Induction of IDO by bacille Calmette-Guérin is responsible for development of murine depressive-like behavior.

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Journal:  J Clin Invest       Date:  2008-10       Impact factor: 14.808

9.  Aging exacerbates depressive-like behavior in mice in response to activation of the peripheral innate immune system.

Authors:  Jonathan P Godbout; Maïté Moreau; Jacques Lestage; Jing Chen; Nathan L Sparkman; Jason O'Connor; Nathalie Castanon; Keith W Kelley; Robert Dantzer; Rodney W Johnson
Journal:  Neuropsychopharmacology       Date:  2007-12-12       Impact factor: 7.853

10.  Indoleamine 2,3-dioxygenase overexpression causes kynurenine-modification of proteins, fiber cell apoptosis and cataract formation in the mouse lens.

Authors:  Maneesh Mailankot; Magdalena M Staniszewska; Heather Butler; Moonkyung H Caprara; Scott Howell; Benlian Wang; Catherine Doller; Lixing W Reneker; Ram H Nagaraj
Journal:  Lab Invest       Date:  2009-03-23       Impact factor: 5.662

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