Donepezil markedly potentiates memantine neurotoxicity in the adult rat brain

被引:43
作者
Creeley, Catherine E. [1 ]
Wozniak, David F. [1 ]
Nardi, Anthony [1 ]
Farber, Nuri B. [1 ]
Olney, John W. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
关键词
memantine; donepezil; tacrine; neurotoxicity; vacuoles; NMDA antagonist; cholinergic; Glutamatergic; cell killing; excitotoxic; dendrotoxic;
D O I
10.1016/j.neurobiolaging.2006.10.020
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
The NMDA antagonist, memantine (Namenda), and the cholinesterase, inhibitor, donepezil (Aricept), are currently being used widely, either individually or in combination, for treatment of Alzheimer's disease (AD). NMDA antagonists have both neuroprotective and neurotoxic properties; the latter is augmented by drugs, such as pilocarpine, that increase cholinergic activity. Whether donepezil, by increasing cholinergic activity, might augment memantine's neurotoxic potential has not been investigated. In the present study, we determined that a dose of memantine (20 mg/kg, i.p.), considered to be in the therapeutic (neuroprotective) range for rats, causes a mild neurotoxic reaction in the adult rat brain. Co-administration of memantine (20 or 30 mg/kg) with donepezil (2.5-10 mg/kg) markedly potentiated this neurotoxic reaction, causing neuronal injury at lower doses of memantine, and causing the toxic reaction to become disseminated and lethal to neurons throughout many brain regions. These findings raise questions about using this drug combination in AD, especially in the absence of evidence that the combination is beneficial, or that either drug arrests or reverses the disease process. (C) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:153 / 167
页数:15
相关论文
共 69 条
[1]
ALLEN HL, 1990, SCIENCE, V247, P221, DOI 10.1126/science.2403696
[2]
[Anonymous], RAT BRAIN STEREOTAXI
[3]
Memantine blocks α7*nicotinic acetylcholine receptors more potently than N-methyl-D-aspartate receptors in rat hippocampal neurons [J].
Aracava, Y ;
Pereira, EFR ;
Maelicke, A ;
Albuquerque, EX .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 312 (03) :1195-1205
[4]
Convulsions induced by donepezil [J].
Babic, T ;
Zurak, N .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 66 (03) :410-410
[5]
RESPONSE OF CHRONIC NEUROPATHIC PAIN SYNDROMES TO KETAMINE - A PRELIMINARY-STUDY [J].
BACKONJA, M ;
ARNDT, G ;
GOMBAR, KA ;
CHECK, B ;
ZIMMERMANN, M .
PAIN, 1994, 56 (01) :51-57
[6]
Neuroprotective concentrations of the N-methyl-D-aspartate open-channel blocker memantine are effective without cytoplasmic vacuolation following post-ischemic administration and do not block maze learning or long-term potentiation [J].
Chen, HSV ;
Wang, YF ;
Rayudu, PV ;
Edgecomb, P ;
Neill, JC ;
Segal, MM ;
Lipton, SA ;
Jensen, FE .
NEUROSCIENCE, 1998, 86 (04) :1121-1132
[7]
EXCITOTOXIC CELL-DEATH [J].
CHOI, DW .
JOURNAL OF NEUROBIOLOGY, 1992, 23 (09) :1261-1276
[8]
KETAMINE, PHENCYCLIDINE, AND MK-801 PROTECT AGAINST KAINIC ACID-INDUCED SEIZURE-RELATED BRAIN-DAMAGE [J].
CLIFFORD, DB ;
OLNEY, JW ;
BENZ, AM ;
FULLER, TA ;
ZORUMSKI, CF .
EPILEPSIA, 1990, 31 (04) :382-390
[9]
THE FUNCTIONAL-ANATOMY AND PATHOLOGY OF LITHIUM PILOCARPINE AND HIGH-DOSE PILOCARPINE SEIZURES [J].
CLIFFORD, DB ;
OLNEY, JW ;
MANIOTIS, A ;
COLLINS, RC ;
ZORUMSKI, CF .
NEUROSCIENCE, 1987, 23 (03) :953-968
[10]
Multifocal brain damage induced by phencyclidine is augmented by pilocarpine [J].
Corso, TD ;
Sesma, MA ;
Tenkova, TI ;
Der, TC ;
Wozniak, DF ;
Farber, NB ;
Olney, JW .
BRAIN RESEARCH, 1997, 752 (1-2) :1-14