Apoptotic mechanisms involved in neurodegenerative diseases:: Experimental and therapeutic approaches

被引:83
作者
Camins, A. [1 ]
Pallas, M. [1 ]
Silvestre, J. S. [2 ]
机构
[1] Univ Barcelona, Nucl Univ Pedralbes, Unitat Farmacol & Farmacognosia, Fac Farm, E-08028 Barcelona, Spain
[2] Prous Science, Dept Pharmacol, Barcelona, Spain
来源
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY | 2008年 / 30卷 / 01期
关键词
antioxidants; apoptosis; COX-2; cyclin-dependent kinases; glutamate receptors; neuronal cell death; p53;
D O I
10.1358/mf.2008.30.1.1090962
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease (AD) and Parkinson's disease (PD) are two of the most significant neurodegenerative disorders in the developed world. However, although these diseases were described almost a century ago, the molecular mechanisms that lead to the neuronal cell death associated with these diseases are not yet clear, and vigorous research efforts have failed to identify effective treatment options. In the present review, we evaluate the potential mechanisms underlying apoptosis and neuronal death in neurodegenerative disorders. A role for mitochondria in the release of proapoptotic proteins, such as cytochrome c and apoptosis-inducing factor (AIF) etc., is discussed along with key processes involving oxidative stress and activation of glutamate receptors. We also deliberate the implication of DNA damage, primarily p53 induction and reentry in the cell cycle. Finally, we postulate that multitargeting therapies comprising antioxidants, cell cycle inhibitors and modulating agents of COX-2 or c-JUN kinase pathways could be suitable strategies to prevent or delay the process of neuronal cell death in neurodegenerative disorders. Thus, the aim of this review is to discuss the pathways involved in the pathogenesis of neurodegenerative diseases such as AD, PD and Huntington's disease (HD). Furthermore, current and future pharmacotherapeutics will be considered. (c) 2008 Prous Science, S.A.U. or its licensors. All rights reserved.
引用
收藏
页码:43 / 65
页数:23
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