Implications for the Kynurenine Pathway and Quinolinic Acid in Amyotrophic Lateral Sclerosis

被引:81
作者
Guillemin, Gilles J. [1 ,2 ,3 ]
Meininger, Vincent [4 ]
Brew, Bruce J. [5 ]
机构
[1] St Vincents Hosp, Ctr Immunol, Sydney, NSW 2010, Australia
[2] Univ New S Wales, Sch Med, Sydney, NSW, Australia
[3] Sch Med Sci, Sydney, NSW, Australia
[4] Hop La Pitie Salpetriere, Ctr SLA Salpetriere Federat Neurol, Paris, France
[5] St Vincents Hosp, Dept Neurol, Sydney, NSW 2010, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Kynurenine pathway; Quinolinic acid; ALS; toxicity pathways;
D O I
10.1159/000089622
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The kynurenine pathway (KP) is a major route of L-tryptophan catabolism leading to production of several neurobiologically active molecules. Among them is the excitotoxin quinolinic acid (QUIN) that is known to be involved in the pathogenesis of several major inflammatory neurological diseases. In amyotrophic lateral sclerosis (ALS) degeneration of motor neurons is associated with a chronic and local infl ammation (presence of activated microglia and astrocytes). There is emerging evidence that the KP is important in ALS. Recently, we demonstrated that QUIN is significantly increased in serum and CSF of ALS patients. Moreover, most of the factors associated with QUIN toxicity are found in ALS, implying that QUIN may play a substantial role in the neuropathogenesis of ALS. This review details the potential role the KP has in ALS and advances a testable hypothetical model. Copyright (C) 2005 S. Karger AG, Basel
引用
收藏
页码:166 / 176
页数:11
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