Back to Search
Start Over
Memantine improves cognition and reduces Alzheimer's-like neuropathology in transgenic mice
- Source :
- The American journal of pathology. 176(2)
- Publication Year :
- 2010
-
Abstract
- 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 (Abeta), Abeta dodecamers (Abeta*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 Abeta-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.
- Subjects :
- Genetically modified mouse
Male
Amyloid
Pathology
medicine.medical_specialty
Aging
medicine.drug_class
Concept Formation
Drug Evaluation, Preclinical
Mice, Transgenic
tau Proteins
Neuropathology
Hippocampal formation
Pharmacology
Pathology and Forensic Medicine
Antiparkinson Agents
Mice
Degenerative disease
Cognition
Species Specificity
Alzheimer Disease
Memantine
Commentaries
mental disorders
Humans
Medicine
Animals
Phosphorylation
Clinical Trials as Topic
Amyloid beta-Peptides
business.industry
Age Factors
Long-term potentiation
medicine.disease
Receptor antagonist
Disease Models, Animal
Female
Alzheimer's disease
Protein Multimerization
business
Protein Kinases
Regular Articles
medicine.drug
Subjects
Details
- ISSN :
- 15252191
- Volume :
- 176
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- The American journal of pathology
- Accession number :
- edsair.doi.dedup.....bd70f333f474d1fd6de25ce97ccb220a