Indoleamine-2,3-dioxygenase activity in experimental human endotoxemia

Background: Excessive tryptophan metabolism to kynurenine by the rate-limiting enzyme endothelial indoleamine 2,3-dioxygenase 1 (IDO) controls arterial vessel relaxation and causes hypotension in murine endotoxemia. However, its relevance in human endotoxemia has not been investigated so far. We thu...

Verfasser: Padberg, Jan
Meurs, Matijs van
Kielstein, Jan T.
Martens-Lobenhoffer, Jens
Bode-Böger, Stefanie M.
Zijlstra, Jan G.
Kovesdy, Csaba P.
Kümpers, Philipp
FB/Einrichtung:FB 05: Medizinische Fakultät
Dokumenttypen:Artikel
Medientypen:Text
Erscheinungsdatum:2012
Publikation in MIAMI:11.03.2013
Datum der letzten Änderung:16.04.2019
Angaben zur Ausgabe:[Electronic ed.]
Quelle:Experimental & Translational Stroke Medicine 4 (2012) 24 http://dx.doi.org/doi:10.1186/2040-7378-4-24
Fachgebiet (DDC):610: Medizin und Gesundheit
Lizenz:CC BY 2.0
Sprache:Englisch
Anmerkungen:Finanziert durch den Open-Access-Publikationsfonds 2012/2013 der Deutschen Forschungsgemeinschaft (DFG) und der Westfälischen Wilhelms-Universität Münster (WWU Münster).
Format:PDF-Dokument
URN:urn:nbn:de:hbz:6-97359453441
Weitere Identifikatoren:DOI: doi:10.1186/2040-7378-4-24
Permalink:https://nbn-resolving.de/urn:nbn:de:hbz:6-97359453441
Onlinezugriff:2040-7378-4-24.pdf

Background: Excessive tryptophan metabolism to kynurenine by the rate-limiting enzyme endothelial indoleamine 2,3-dioxygenase 1 (IDO) controls arterial vessel relaxation and causes hypotension in murine endotoxemia. However, its relevance in human endotoxemia has not been investigated so far. We thus aimed to study changes in blood pressure in parallel with tryptophan and kynurenine levels during experimental endotoxemia in humans. Findings: Six healthy male volunteers were given E. coli lipopolysaccharide (LPS; 4 ng/kg) as a 1-min intravenous infusion. They had levels of soluble E-Selectin and soluble vascular cell adhesion molecule-1 as well as IDO activity assessed as the kynurenine-to-tryptophan plasma ratio by liquid chromatography-tandem mass spectrometry at various time points during a 24 h time course. During endotoxemia, IDO activity significantly increased, reaching peak levels at 8 h after LPS infusion (44.0 ± 15.2 vs. 29.4 ± 6.8 at baseline, P