Combination of memantine and vitamin D prevents axon degeneration induced by amyloid-beta and glutamate

被引:48
|
作者
Annweiler, Cedric [1 ,2 ,3 ,4 ]
Brugg, Bernard [5 ]
Peyrin, Jean-Michel [5 ]
Bartha, Robert [4 ]
Beauchet, Olivier [1 ,2 ,3 ]
机构
[1] Angers Univ Hosp, Dept Neurosci, Div Geriatr Med, F-49933 Angers 9, France
[2] Univ Memory Clin, Angers, France
[3] Univ Angers, UNAM, UPRES EA 4638, Angers, France
[4] Univ Western Ontario, Dept Med Biophys, Robarts Res Inst, Schulich Sch Med & Dent, London, ON, Canada
[5] Univ Paris 06, UMR NPA 7102, Paris, France
关键词
Alzheimer's disease; Amyloid-beta; Glutamate; Memantine; Vitamin D; Neuroprotection; DISEASE; NEUROPROTECTION; TRANSPORT; COGNITION; DECREASE; NEURONS; PLAQUES;
D O I
10.1016/j.neurobiolaging.2013.07.029
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The currently available drugs for treatment of Alzheimer's disease are symptomatic and only temporarily slow down the natural history of the disease process. Recently, its has been proposed that the combination of memantine with vitamin D, a neurosteroid hormone, may prevent amyloid-beta and glutamate neurotoxicity. Here, our purpose was to examine the potential protective effects of memantine and vitamin D against amyloid-beta peptide and glutamate toxicity in cortical neuronal cultures. We provide the first evidence that cortical axons degenerate less after exposure to amyloid-beta peptide or glutamate in microfluidic neuronal cultures enriched with memantine plus vitamin D compared to control medium and cultures enriched with only memantine or only vitamin D. The reported synergistic neuroprotective effect of memantine plus vitamin D-the combination originating an effect stronger than the sum-corroborate previous clinical finding that Alzheimer's disease patients using this drug combination have improved cognition. This finding reinforces the pharmacological potential of a new drug combining memantine plus vitamin D for the treatment or the prevention of Alzheimer's disease. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:331 / 335
页数:5
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