A preclinical view of cholinesterase inhibitors in neuroprotection: do they provide more than symptomatic benefits in Alzheimer's disease?

被引:119
作者
Francis, PT
Nordberg, A
Arnold, SE
机构
[1] Univ London Kings Coll, Wolfson Ctr Age Related Dis, London SE1 1UL, England
[2] Karolinska Univ Hosp Huddinge, Karolinska Inst, Neurotec Dept, Div Mol Neuropharmacol, Stockholm, Sweden
[3] Univ Penn, Dept Psychiat, Ctr Neurobiol & Behav, Cellular & Mol Neuropathol Program, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/j.tips.2004.12.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The prevalence of Alzheimer's disease (AD), a neurodegenerative condition whose greatest risk factor is old age, is expected to rise dramatically during the next five decades, along with the trend for increased longevity. Early diagnosis and intervention with therapies that halt or slow disease progress are likely to represent an important component of effective treatment. Although much progress has been made in this area, there are currently no clinically approved interventions for AD that are classed as disease modifying or neuroprotective. Cholinesterase inhibitors are a drug class used for the symptomatic treatment of AD. Recent evidence from preclinical studies indicates that these agents can attenuate neuronal damage and death from cytotoxic insults, and therefore might affect AD pathogenesis. The mechanisms by which these actions are mediated might or might not be directly related to their primary mode of action.
引用
收藏
页码:104 / 111
页数:8
相关论文
共 68 条
[31]   Characterization of the effect of ganstigmine (CHF2819) on amyloid precursor protein metabolism in SH-SY5Y neuroblastoma cells [J].
Mazzucchelli, M ;
Porrello, E ;
Villetti, G ;
Pietra, C ;
Govoni, S ;
Racchi, M .
JOURNAL OF NEURAL TRANSMISSION, 2003, 110 (08) :935-947
[32]  
MCKHANN G, 1984, NEUROLOGY, V34, P939, DOI 10.1212/WNL.34.7.939
[33]   Drugs targeting Alzheimer's disease: Some things old and some things new [J].
Michaelis, ML .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (03) :897-904
[34]   Chronic nicotine treatment reduces β-amyloidosis in the brain of a mouse model of Alzheimer's disease (APPsw) [J].
Nordberg, A ;
Hellström-Lindahl, E ;
Lee, M ;
Johnson, M ;
Mousavi, M ;
Hall, R ;
Perry, E ;
Bednar, I ;
Court, J .
JOURNAL OF NEUROCHEMISTRY, 2002, 81 (03) :655-658
[35]   The Role of Neuronal Nicotinic Acetylcholine Receptors in Acute and Chronic Neurodegeneration [J].
O'Neill, M. J. ;
Murray, T. K. ;
Lakics, V ;
Visanji, N. P. ;
Duty, S. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2002, 1 (04) :399-411
[36]   Comparison of inhibitory activities of donepezil and other cholinesterase inhibitors on acetylcholinesterase and butyrylcholinesterase in vitro [J].
Ogura, H ;
Kosasa, T ;
Kuriya, Y ;
Yamanishi, Y .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2000, 22 (08) :609-613
[37]   Role of Acetylcholinesterase Inhibitors in the Metabolism of Amyloid Precursor Protein [J].
Pakaski, M. ;
Kasa, P. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2003, 2 (03) :163-171
[38]   Mitochondrial mechanisms of neural cell apoptosis [J].
Polster, BM ;
Fiskum, G .
JOURNAL OF NEUROCHEMISTRY, 2004, 90 (06) :1281-1289
[39]   Short- and long-term effect of acetylcholinesterase inhibition on the expression and metabolism of the amyloid precursor protein [J].
Racchi, M ;
Sironi, M ;
Caprera, A ;
König, G ;
Govoni, S .
MOLECULAR PSYCHIATRY, 2001, 6 (05) :520-528
[40]   Acetylcholinesterase inhibitors: novel activities of old molecules [J].
Racchi, M ;
Mazzucchelli, M ;
Porrello, E ;
Lanni, C ;
Govoni, S .
PHARMACOLOGICAL RESEARCH, 2004, 50 (04) :441-451