An expanding range of targets for kynurenine metabolites of tryptophan

被引:273
作者
Stone, Trevor W. [1 ]
Stoy, Nicholas [1 ]
Darlington, L. Gail [1 ]
机构
[1] Univ Glasgow, Inst Neurosci & Psychol, Coll Med Vet & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
关键词
ARYL-HYDROCARBON RECEPTOR; ALPHA-7 NICOTINIC RECEPTOR; REGULATORY T-CELLS; PROTEIN-COUPLED RECEPTOR; RAT HIPPOCAMPAL SLICES; MOUSE ASTROGLIAL CELLS; QUINOLINIC ACID; HUNTINGTONS-DISEASE; ALZHEIMERS-DISEASE; DENDRITIC CELLS;
D O I
10.1016/j.tips.2012.09.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The kynurenine pathway of tryptophan. metabolism accounts for most of the tryptophan that is not committed to protein synthesis and includes compounds active in the nervous and immune systems. Kynurenine acts on the aryl hydrocarbon receptor, affecting the metabolism of xenobiotics and promoting carcinogenesis. Quinolinic acid is an agonist at N-methyl-D-aspartate receptors (NMDARs), but is also pro-oxidant, has immunomodulatory actions, and promotes the formation of hyperphosphorylated tau proteins. Kynurenic acid blocks NMDARs and alpha 7-homomeric nicotinic cholinoceptors and is also an agonist at the orphan G-protein-coupled receptor GPR35. 3-Hydroxykynurenine and 3-hydroxyanthranilic acid have pronounced redox activity and regulate T cell function. Cinnabarinic acid can activate metabotropic glutamate receptors. This review highlights the increasing range of molecular targets for components of the kynurenine pathway in both the nervous and immune systems in relation to their relevance to disease and drug development.
引用
收藏
页码:136 / 143
页数:8
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