Oral Administration of Synthetic Retinoid Am80 (Tamibarotene) Decreases Brain β-Amyloid Peptides in APP23 Mice

被引:33
作者
Kawahara, Kohichi [1 ]
Nishi, Kentaro [1 ]
Suenobu, Michita [1 ]
Ohtsuka, Hideyuki [1 ]
Maeda, Akira [1 ]
Nagatomo, Kenichiro [1 ]
Kuniyasu, Akihiko [1 ]
Staufenbiel, Matthias [2 ]
Nakagomi, Madoka [3 ]
Shudo, Koichi [3 ]
Nakayama, Hitoshi [1 ]
机构
[1] Kumamoto Univ, Dept Mol Cell Funct, Grad Sch Med & Pharmaceut Sci, Kumamoto 8620973, Japan
[2] Novartis Inst BioMed Res Basel, Nervous Syst Dept, CH-4002 Basel, Switzerland
[3] Res Fdn Itsuu Lab, Setagaya Ku, Tokyo 1580094, Japan
关键词
retinoid; Am80; tamibarotene; Alzheimer's disease; beta-amyloid; ALZHEIMER-DISEASE; CELLS; ACID; DEPOSITION; CLEARANCE; RESCUES;
D O I
10.1248/bpb.32.1307
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study is to investigate whether a synthetic retinoid Am80 (tamibarotene) exhibits any improving effects on amyloid precursor protein (APP)23 mice, a model of Alzheimer's disease. Am80 was orally administered in feed to 20-week (5-month)-old APP23 mice at a dose of 0 (control) or 0.5mg/kg/d for 14 weeks. The Am80 treatment reduced significantly the insoluble A beta levels in brain, in particular A beta(42), while it gave no apparent effects on the soluble A beta levels. The results suggest that oral administration of Am80 may have potency to reduce the extracellular A beta(42) of insoluble and possibly oligomeric or protofibril forms, which are related to the cause and/or progression of Alzheimer's disease. The Am80 treatment showed no significant effect on spatial learning and memory of APP23 mice by Morris water maze analysis. The main reason for the absence of significance seems based on the large deviation and some mice both in the treated and the non-treated groups would neither swim nor make efforts to reach the platform.
引用
收藏
页码:1307 / 1309
页数:3
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