Unique pharmacological property of ISRIB in inhibition of Aβ-induced neuronal cell death

被引:25
|
作者
Hosoi, Toru [1 ]
Kakimoto, Mai [1 ]
Tanaka, Keigo [1 ]
Nomura, Jun [2 ]
Ozawa, Koichiro [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Pharmacotherapy, 1-2-3 Kasumi, Hiroshima 7348553, Japan
[2] RIKEN Brain Sci Inst, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
关键词
Amyloid beta; Alzheimer's disease; ISRIB; ALZHEIMERS-DISEASE; PROTEIN; STRESS; EIF2-ALPHA; SIGNAL; GENE;
D O I
10.1016/j.jphs.2016.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A pharmacological approach to ameliorate Alzheimer's disease (AD) has not yet been established. In the present study, we investigated the pharmacological characteristics of the recently identified memory-enhancing compound, ISRIB for the amelioration of AD. ISRIB potently attenuated amyloid beta-induced neuronal cell death at concentrations of 12.5-25 nM, but did not inhibit amyloid beta production in the HEK293T cell line expressing the amyloid precursor protein (APP). These results suggest that ISRIB possesses the unique pharmacological property of attenuating amyloid beta-induced neuronal cell death without affecting amyloid b production. (C) 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
引用
收藏
页码:292 / 295
页数:4
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