Paradigm shift in neuroprotection by NMDA receptor blockade: Memantine and beyond
By S. Lipton. Nature reviews. Drug discovery, 2006
920 citations recorded by the source corpus.
Subfields: Biochemistry, Cellular and Molecular Neuroscience, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1bfed17975c539402d60536439fb5a8ddbf8f971
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In Biochemistry
In Cellular and Molecular Neuroscience
In Molecular Biology
Citations in the corpus
- Memantine: a NMDA receptor antagonist that improves memory by restoration of homeostasis in the glutamatergic system--too little activation is bad, too much is even worse. (2007, background): “Rogawski and Wenk, 2003; Lipton, 2006; Wenk et al., 2006; Bullock, 2006).”
- Aβ Oligomer-Induced Aberrations in Synapse Composition, Shape, and Density Provide a Molecular Basis for Loss of Connectivity in Alzheimer's Disease (2007, background): “Because the Alzheimer’s drug Namenda (memantine) is thought to function therapeutically as an openchannel blocker of NMDA receptors (Lipton, 2006) and NMDA receptors codistribute in hippocampal cultures with ADDLs, we tested whether memantine might exhibit efficacy in blocking ADDL-induced drebrin…”
- Oxidative Stress, Synaptic Dysfunction, and Alzheimer’s Disease (2017, background): “Importantly, memantine has greater affinity to non-synaptic NMDA receptors, which are implicated in excitotoxicity associated with the glutamate spillover and have distinctly different composition of receptor subunits [164, 165].”