Kynurenines, neurodegeneration and Alzheimer's disease.

Abstract

Alzheimer's disease (AD) is one of the major causes of dementia. The pathogenesis of the disease is not entirely understood, but the amyloid β peptide (Aβ) and the formation of senile plaques seem to play pivotal roles. Oligomerization of the Aβ is thought to trigger a cascade of events, including oxidative stress, glutamate excitotoxicity and inflammation. The kynurenine (KYN) pathway is the major route for the metabolism of the essential amino acid tryptophan. Some of the metabolites of this pathway, such as 3-hydroxykynurenine and quinolinic acid, are known to have neurotoxic properties, whereas others, such as kynurenic acid, are putative neuroprotectants. Among other routes, the KYN pathway has been shown to be involved in AD pathogenesis, and connections to other known mechanisms have also been demonstrated. Oxidative stress, glutamate excitotoxicity and the neuroinflammation involved in AD pathogenesis have been revealed to be connected to the KYN pathway. Intervention at these key steps may serve as the aim of potential therapy.

• Authors: Zsigmond Tamas Kincses, József Toldi, László Vécsei
• Journal: Journal of cellular and molecular medicine (J Cell Mol Med) Vol. 14 Issue 8 Pg. 2045-54 (Aug 2010) ISSN: 1582-4934 [Electronic] England
• PMID: 20629991 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
• Copyright: © 2010 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.

Chemical References

• Amyloid beta-Peptides
• Kynurenine
• Tryptophan
• Quinolinic Acid

Topics

• Alzheimer Disease (etiology, metabolism)
• Amyloid beta-Peptides (metabolism)
• Biosynthetic Pathways
• Humans
• Kynurenine (chemistry, metabolism)
• Molecular Structure
• Nerve Degeneration (complications, metabolism)
• Plaque, Amyloid (metabolism)
• Quinolinic Acid (chemistry, metabolism)
• Tryptophan (chemistry, metabolism)