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[Memantine: a therapeutic drug for Alzheimer's disease and the comparison with MK-801].
- Source :
-
Nihon yakurigaku zasshi. Folia pharmacologica Japonica [Nihon Yakurigaku Zasshi] 2004 Sep; Vol. 124 (3), pp. 145-51. - Publication Year :
- 2004
-
Abstract
- Memantine is agreed officially as a therapeutic drug for moderate-to-severe Alzheimer's disease (AD) in EU and USA. Memantine is a similar uncompetitive NMDA-receptor antagonist to MK-801 and phencyclidine (PCP), and it prevents nerve cell death induced by the ischemia which induces as excessive release of glutamate. These medicines act on an ion channel binding site similar to the magnesium ion binding site. However, MK-801 and PCP cause schizophrenic symptoms, so they are not being used as a therapeutic drug for AD. Memantine does not have those toxicities and does not stimulate acetylcholine release in the cerebral cortex. Although the mechanism of the difference from memantine and MK-801 has not been made clear yet, it seems that memantine is combined and released with the ion channel depending on electric potential in the same way as the magnesium ion. Basic and clinical research will clarify the control mechanism of memantine.
- Subjects :
- Binding Sites
Controlled Clinical Trials as Topic
Dizocilpine Maleate adverse effects
Dizocilpine Maleate chemistry
Drug Design
Excitatory Amino Acid Antagonists pharmacology
Glutamates metabolism
Humans
Ion Channels metabolism
Magnesium physiology
Memantine chemistry
Memantine metabolism
Receptors, N-Methyl-D-Aspartate metabolism
Severity of Illness Index
Alzheimer Disease drug therapy
Dizocilpine Maleate pharmacology
Excitatory Amino Acid Antagonists therapeutic use
Memantine pharmacology
Memantine therapeutic use
Receptors, N-Methyl-D-Aspartate antagonists & inhibitors
Subjects
Details
- Language :
- Japanese
- ISSN :
- 0015-5691
- Volume :
- 124
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Nihon yakurigaku zasshi. Folia pharmacologica Japonica
- Publication Type :
- Academic Journal
- Accession number :
- 15333987
- Full Text :
- https://doi.org/10.1254/fpj.124.145