Valsartan lowers brain β-amyloid protein levels and improves spatial learning in a mouse model of Alzheimer disease

被引:266
作者
Wang, Jun
Ho, Lap
Chen, Linghong
Zhao, Zhong
Zhao, Wei
Qian, Xianjuan
Humala, Nelson
Seror, Ilana
Bartholomew, Sadie
Rosendorff, Clive
Pasinetti, Giulio Maria
机构
[1] CUNY Mt Sinai Sch Med, Icahn Res Inst, Dept Psychiat, New York, NY 10029 USA
[2] James J Peters Vet Affairs Med Ctr, Ctr Geriatr Res Educ & Clin, New York, NY USA
[3] CUNY Mt Sinai Sch Med, Dept Med, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Dept Neurosci, New York, NY 10029 USA
关键词
D O I
10.1172/JCI31547
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Recent epidemiological evidence suggests that some antihypertensive medications may reduce the risk for Alzheimer disease (AD). We screened 55 clinically prescribed antihypertensive medications for AD-modifying activity using primary cortico-hippocampal neuron cultures generated from the Tg2576 AD mouse model. These agents represent all drug classes used for hypertension pharmacotherapy. We identified 7 candidate antihypertensive agents that significantly reduced AD-type P-amyloid protein (A beta) accumulation. Through in vitro studies, we found that only 1 of the candidate drugs, valsartan, was capable of attenuating oligomerization of A beta peptides into high-molecular-weight (HMW) oligomeric peptides, known to be involved in cognitive deterioration. We found that preventive treatment of Tg2576 mice with valsartan significantly reduced AD-type neuropathology and the content of soluble HMW extracellular oligomeric AP peptides in the brain. Most importantly, valsartan administration also attenuated the development of A beta-mediated cognitive deterioration, even when delivered at a dose about 2-fold lower than that used for hypertension treatment in humans. These preclinical studies suggest that certain antihypertensive drugs may have AD-modifying activity and may protect against progressive A beta-related memory deficits in subjects with AD or in those at high risk of developing AD.
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页码:3393 / 3402
页数:10
相关论文
共 38 条
[1]  
[Anonymous], 2002, CALAMUS RENASCENS
[2]   GENERATION OF BETA-AMYLOID IN THE SECRETORY PATHWAY IN NEURONAL AND NONNEURONAL CELLS [J].
BUSCIGLIO, J ;
GABUZDA, DH ;
MATSUDAIRA, P ;
YANKNER, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :2092-2096
[3]   Natural oligomers of the amyloid-protein specifically disrupt cognitive function [J].
Cleary, JP ;
Walsh, DM ;
Hofmeister, JJ ;
Shankar, GM ;
Kuskowski, MA ;
Selkoe, DJ ;
Ashe, KH .
NATURE NEUROSCIENCE, 2005, 8 (01) :79-84
[4]   CLEAVAGE OF AMYLOID-BETA PEPTIDE DURING CONSTITUTIVE PROCESSING OF ITS PRECURSOR [J].
ESCH, FS ;
KEIM, PS ;
BEATTIE, EC ;
BLACHER, RW ;
CULWELL, AR ;
OLTERSDORF, T ;
MCCLURE, D ;
WARD, PJ .
SCIENCE, 1990, 248 (4959) :1122-1124
[5]   The prevention of dementia with antihypertensive treatment [J].
Forette, F ;
Seux, ML ;
Staessen, JA ;
Thijs, L ;
Babarskiene, MR ;
Babeanu, S ;
Bossini, A ;
Fagard, R ;
Gil-Extremera, B ;
Laks, T ;
Kobalava, Z ;
Sarti, C ;
Tuomilehto, J ;
Vanhanen, H ;
Webster, J ;
Yodfat, Y ;
Birkenhäger, WH .
ARCHIVES OF INTERNAL MEDICINE, 2002, 162 (18) :2046-2052
[6]   Low blood pressure and incidence of dementia in a very old sample: Dependent on initial cognition [J].
Guo, ZC ;
Viitanen, M ;
Winblad, B ;
Fratiglioni, L .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1999, 47 (06) :723-726
[7]   AMYLOID BETA-PEPTIDE IS PRODUCED BY CULTURED-CELLS DURING NORMAL METABOLISM [J].
HAASS, C ;
SCHLOSSMACHER, MG ;
HUNG, AY ;
VIGOPELFREY, C ;
MELLON, A ;
OSTASZEWSKI, BL ;
LIEBERBURG, I ;
KOO, EH ;
SCHENK, D ;
TEPLOW, DB ;
SELKOE, DJ .
NATURE, 1992, 359 (6393) :322-325
[8]   Diet-induced insulin resistance promotes amyloidosis in a transgenic mouse model of Alzheimer's disease [J].
Ho, L ;
Qin, WP ;
Pompl, PN ;
Xiang, ZM ;
Wang, J ;
Zhao, Z ;
Peng, YZ ;
Cambareri, G ;
Rocher, A ;
Mobbs, CV ;
Hof, PR ;
Pasinetti, GM .
FASEB JOURNAL, 2004, 18 (03) :902-+
[9]   Correlative memory deficits, A beta elevation, and amyloid plaques in transgenic mice [J].
Hsiao, K ;
Chapman, P ;
Nilsen, S ;
Eckman, C ;
Harigaya, Y ;
Younkin, S ;
Yang, FS ;
Cole, G .
SCIENCE, 1996, 274 (5284) :99-102
[10]  
INTVELD BA, 2000, NEUROBIOL AGING, V54, pA397