Reduced levels of Aβ 40 and Aβ 42 in brains of smoking controls and Alzheimer's patients

被引:66
作者
Hellström-Lindahl, E
Mousavi, M
Ravid, R
Nordberg, A
机构
[1] Huddinge Univ Hosp, Dept Neurotec, Div Mol Neuropharmacol, Karolinska Inst, S-14186 Huddinge, Sweden
[2] Netherlands Brain Bank, Amsterdam, Netherlands
基金
瑞典研究理事会;
关键词
Alzheimer's disease; amyloid beta peptide; human brain; nicotine; nicotinic receptors; smoking;
D O I
10.1016/j.nbd.2003.11.024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of nicotine on levels of Abeta 40 and Abeta 42 and nicotinic receptor binding sites were studied in brains from nonsmoking and smoking patients with Alzheimer's disease (AD) and aged-matched controls. The levels of soluble and insoluble Abeta 40 and Abeta 42 in frontal cortex and Abeta 40 in temporal cortex and hippocampus were significantly decreased in smoking AD patients compared to nonsmokers with AD. In smoking controls the levels of soluble and insoluble Abeta 40 and Abeta 42 in the frontal and temporal cortex were significantly lower than in nonsmoking controls. The binding of [H-3]cytisine in temporal cortex was significantly increased in smokers with AD compared to nonsmokers with AD. In smoking controls [H-3]cytisine and [H-3]epibatidine binding were significantly increased from 1.5- to 2-fold compared to nonsmoking controls whereas binding sites for [I-125]alpha-bungarotoxin was less up-regulated. These results indicate that selective nicotinic receptor agonists may be a novel protective therapy in AD by reducing Abeta levels as well as the loss of nicotinic receptors in AD brain. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:351 / 360
页数:10
相关论文
共 77 条
[1]   Smoking as a risk factor for Alzheimer's disease: contrasting evidence from a systematic review of case-control and cohort studies [J].
Almeida, OP ;
Hulse, GK ;
Lawrence, D ;
Flicker, L .
ADDICTION, 2002, 97 (01) :15-28
[2]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[3]   Selective nicotinic receptor consequences in APPSWE transgenic mice [J].
Bednar, I ;
Paterson, D ;
Marutle, A ;
Pham, TM ;
Svedberg, M ;
Hellström-Lindahl, E ;
Mousavi, M ;
Court, J ;
Morris, C ;
Perry, E ;
Mohammed, A ;
Zhang, X ;
Nordberg, A .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2002, 20 (02) :354-365
[4]  
Bednar I, 2002, NEUROBIOL AGING, V23, pS270
[5]   EVIDENCE THAT TOBACCO SMOKING INCREASES THE DENSITY OF (-)-[H-3]NICOTINE BINDING-SITES IN HUMAN-BRAIN [J].
BENWELL, MEM ;
BALFOUR, DJK ;
ANDERSON, JM .
JOURNAL OF NEUROCHEMISTRY, 1988, 50 (04) :1243-1247
[6]  
Braak H, 1996, ACTA NEUROL SCAND, V93, P3
[7]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[8]  
Breese CR, 1997, J PHARMACOL EXP THER, V282, P7
[9]  
Burghaus L, 2000, MOL BRAIN RES, V76, P385
[10]   Alzheimer-like neurodegeneration in aged antinerve growth factor transgenic mice [J].
Capsoni, S ;
Ugolini, G ;
Comparini, A ;
Ruberti, F ;
Berardi, N ;
Cattaneo, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6826-6831