On the Biological Importance of the 3-hydroxyanthranilic Acid: Anthranilic Acid Ratio

被引:123
作者
Darlington, L. Gail [1 ]
Forrest, Caroline M. [2 ]
Mackay, Gillian M. [2 ]
Smith, Robert A. [2 ]
Smith, Andrew J. [2 ]
Stoy, Nicholas [3 ]
Stone, Trevor W. [2 ]
机构
[1] Epsom Gen Hosp, Epsom KT18 7EG, Surrey, England
[2] Univ Glasgow, Fac Biomed & Life Sci, Neurosci & Mol Pharmacol, Glasgow G12 8QQ, Lanark, Scotland
[3] Royal Hosp Neurodisabil, London SW15 3SW, England
来源
INTERNATIONAL JOURNAL OF TRYPTOPHAN RESEARCH | 2010年 / 3卷
关键词
anthranilic acid; 3-hydroxyanthranilic acid; inflammation; Huntington's disease; stroke; kynurenines;
D O I
10.4137/IJTR.S4282
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Of the major components of the kynurenine pathway for the oxidative metabolism of tryptophan, most attention has focussed on the N-methyl-D-aspartate (NMDA) receptor agonist quinolinic acid, and the glutamate receptor blocker kynurenic acid. However, there is increasing evidence that the redox-active compound 3-hydroxyanthranilic acid may also have potent actions on cell function in the nervous and immune systems, and recent clinical data show marked changes in the levels of this compound, associated with changes in anthranilic acid levels, in patients with a range of neurological and other disorders including osteoporosis, chronic brain injury, Huntington's disease, coronary heart disease, thoracic disease, stroke and depression. In most cases, there is a decrease in 3-hydroxyanthranilic acid levels and an increase in anthranilic acid levels. In this paper, we summarise the range of data obtained to date, and hypothesise that the levels of 3-hydroxyanthranilic acid or the ratio of 3-hydroxyanthranilic acid to anthranilic acid levels, may contribute to disorders with an inflammatory component, and may represent a novel marker for the assessment of inflammation and its progression. Data are presented which suggest that the ratio between these two compounds is not a simple determinant of neuronal viability. Finally, a hypothesis is presented to account for the development of the observed changes in 3-hydroxyanthranilic acid and anthranilate levels in inflammation and it is suggested that the change of the 3HAA:AA ratio, particularly in the brain, could possibly be a protective response to limit primary and secondary damage.
引用
收藏
页码:51 / 59
页数:9
相关论文
共 43 条
[1]  
BARAN H, 1991, ADV EXP MED BIOL, V294, P485
[2]   KYNURENIC ACID ANTAGONISES RESPONSES TO NMDA VIA AN ACTION AT THE STRYCHNINE-INSENSITIVE GLYCINE RECEPTOR [J].
BIRCH, PJ ;
GROSSMAN, CJ ;
HAYES, AG .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 154 (01) :85-87
[3]   Tissue distribution and turnover of [3H]riboflavin during respiratory infection in mice [J].
Brijlal, S ;
Lakshmi, AV .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1999, 48 (12) :1608-1611
[4]   THE RELATION BETWEEN RIBOFLAVIN AND TRYPTOPHAN METABOLISM, STUDIED IN THE RAT [J].
CHARCONNETHARDING, F ;
DALGLIESH, CE ;
NEUBERGER, A .
BIOCHEMICAL JOURNAL, 1953, 53 (04) :513-521
[5]   Prolonged survival of a murine model of cerebral malaria by kynurenine pathway inhibition [J].
Clark, CJ ;
Mackay, GM ;
Smythe, GA ;
Bustamante, S ;
Stone, TW ;
Phillips, RS .
INFECTION AND IMMUNITY, 2005, 73 (08) :5249-5251
[6]   Suppression of T-cell response and prolongation of allograft survival in a rat model by tryptophan catabolites [J].
Dai, Xiangchen ;
Zhu, Bao Ting .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 606 (1-3) :225-232
[7]   Altered kynurenine metabolism correlates with infarct volume in stroke [J].
Darlington, L. G. ;
Mackay, G. M. ;
Forrest, C. M. ;
Stoy, N. ;
George, C. ;
Stone, T. W. .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2007, 26 (08) :2211-2221
[8]   OXIDATIVE REACTIVITY OF THE TRYPTOPHAN-METABOLITES 3-HYDROXYANTHRANILATE, CINNABARINATE, QUINOLINATE AND PICOLINATE [J].
DYKENS, JA ;
SULLIVAN, SG ;
STERN, A .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (02) :211-217
[9]   T cell apoptosis by tryptophan catabolism [J].
Fallarino, I ;
Grohmann, U ;
Vacca, C ;
Bianchi, R ;
Orabona, C ;
Spreca, A ;
Fioretti, MC ;
Puccetti, P .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (10) :1069-1077
[10]   Kynurenine pathway metabolism in patients with osteoporosis after 2 years of drug treatment [J].
Forrest, Caroline M. ;
Mackay, Gillian M. ;
Oxford, Lynn ;
Stoy, Nicholas ;
Stone, Trevor W. ;
Darlington, L. Gail .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2006, 33 (11) :1078-1087