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.
引用
收藏
页码:3393 / 3402
页数:10
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