Memantine Improves Cognition and Reduces Alzheimer's-Like Neuropathology in Transgenic Mice

被引:180
作者
Martinez-Coria, Hilda [1 ]
Green, Kim N. [1 ]
Billings, Lauren M. [1 ]
Kitazawa, Masashi [1 ]
Albrecht, Miriam [2 ]
Rammes, Gerhard [3 ]
Parsons, Chris G. [2 ]
Gupta, Sandeep [4 ]
Banerjee, Pradeep [4 ]
LaFerla, Frank M. [1 ]
机构
[1] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
[2] Merz Pharmaceut, Frankfurt, Germany
[3] Tech Univ Munich, Dept Anaesthesiol, Munich, Germany
[4] Forest Res Inst, Dept Pharmacol, Jersey City, NJ USA
关键词
LONG-TERM POTENTIATION; NMDA RECEPTOR ANTAGONIST; D-ASPARTATE RECEPTORS; A-BETA OLIGOMERS; IN-VIVO; SYNAPTIC-TRANSMISSION; TAU-PHOSPHORYLATION; TANGLE FORMATION; DISEASE; MODEL;
D O I
10.2353/ajpath.2010.090452
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Memantine is an N-Methyl-D-aspartate receptor antagonist that is approved for the treatment of moderate to severe Alzheimer's disease (AD). in this study, three groups of triple-transgenic (3xTg-AD) mice with differing levels of AD-like pathology (6, 9, and 15 months of age) were treated for 3 months with doses of memantine equivalent to those used in humans. After the treatment, memantine-treated mice had restored cognition and significantly reduced the levels of insoluble amyloid-beta (A beta), A beta dodecamers (A beta(star)56), prefibrillar soluble oligomers, and fibrillar oligomers. The effects on pathology were stronger in older, more impaired animals. Memantine treatment also was associated with a decline in the levels of total tau and hyperphosphorylated tau. Finally, memantine pre-incubation prevented A beta-induced inhibition of long-term potentiation in hippocampal slices of cognitively normal mice. These results suggest that the effects of memantine treatment on AD brain include disease modification and prevention of synaptic dysfunction. (Am J Pathol 2010, 176:870-880; DOI: 10.2353/ajpath.2010.090452)
引用
收藏
页码:870 / 880
页数:11
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