美金刚
NMDA受体
多奈哌齐
谷氨酸的
神经科学
药理学
敌手
神经药理学
心理学
医学
谷氨酸受体
精神科
痴呆
疾病
受体
内科学
作者
Shahrina Alam,Kaelyn S. Lingenfelter,Aaron M. Bender,Craig W. Lindsley
标识
DOI:10.1021/acschemneuro.7b00270
摘要
Memantine was the first breakthrough medication for the treatment of moderate to severe Alzheimer's disease (AD) patients and represents a fundamentally new mechanism of action (moderate-affinity, uncompetitive, voltage-dependent, N-methyl-d-aspartate (NMDA) receptor antagonist that exhibits fast on/off kinetics) to modulate glutamatergic dysfunction. Since its approval by the FDA in 2003, memantine, alone and in combination with donepezil, has improved patient outcomes in terms of cognition, behavioral disturbances, daily functioning, and delaying time to institutionalization. In this review, we will highlight the historical significance of memantine to AD (and other neuropsychiatric disorders) as well as provide an overview of the synthesis, pharmacology, and drug metabolism of this unique NMDA uncompetitive antagonist that clearly secures its place among the Classics in Chemical Neuroscience.
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