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Unique pharmacological property of ISRIB in inhibition of Aß-induced neuronal cell death.
Hosoi, Toru; Kakimoto, Mai; Tanaka, Keigo; Nomura, Jun; Ozawa, Koichiro.
Affiliation
  • Hosoi T; Department of Pharmacotherapy, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan. Electronic address: toruh@hiroshima-u.ac.jp.
  • Kakimoto M; Department of Pharmacotherapy, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.
  • Tanaka K; Department of Pharmacotherapy, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.
  • Nomura J; RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan.
  • Ozawa K; Department of Pharmacotherapy, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan. Electronic address: ozawak@hiroshima-u.ac.jp.
J Pharmacol Sci ; 131(4): 292-5, 2016 Aug.
Article in En | MEDLINE | ID: mdl-27569458
ABSTRACT
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 ß-induced neuronal cell death at concentrations of 12.5-25 nM, but did not inhibit amyloid ß 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 ß-induced neuronal cell death without affecting amyloid ß production.
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Full text: 1 Database: MEDLINE Main subject: Peptide Fragments / Amyloid beta-Peptides / Cell Death / Cyclohexylamines / Acetamides / Neurons Type of study: Prognostic_studies Limits: Humans Language: En Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Peptide Fragments / Amyloid beta-Peptides / Cell Death / Cyclohexylamines / Acetamides / Neurons Type of study: Prognostic_studies Limits: Humans Language: En Year: 2016 Type: Article