Page 77 - AN-1-2
P. 77
Advanced Neurology NMDA receptors in neuropsychiatric diseases
https://doi.org/1113/jphysiol.1973.sp010273 https://doi.org/1016/j.neuron.2005.08.034
131. Collingridge GL, Kehl SJ, McLennan H, 1983, The 143. Lu HC, Gonzalez E, Crair MC, 2001, Barrel cortex critical
antagonism of amino acid-induced excitations of rat period plasticity is independent of changes in NMDA
hippocampal CA1 neurones in vitro. J Physiol, 334: 19–31. receptor subunit composition. Neuron, 32: 619–634.
https://doi.org/1113/jphysiol.1983.sp014477. https://doi.org/1016/s0896-6273(01)00501-3
132. Morris RG, 1989, Synaptic plasticity and learning: Selective 144. Zhao MG, Toyoda H, Lee YS, et al., 2005, Roles of NMDA
impairment of learning rats and blockade of long-term NR2B subtype receptor in prefrontal long-term potentiation
potentiation in vivo by the N-methyl-D-aspartate receptor and contextual fear memory. Neuron, 47: 859-872.
antagonist AP5. J Neurosci, 9: 3040–3057. https://doi.org/1016/j.neuron.2005.08.014
133. Morris RG, Anderson E, Lynch GS, et al., 1986, Selective 145. Akashi K, Kakizaki T, Kamiya H, et al., 2009, NMDA
impairment of learning and blockade of long-term receptor GluN2B (GluR epsilon 2/NR2B) subunit is
potentiation by an N-methyl-D-aspartate receptor crucial for channel function, postsynaptic macromolecular
antagonist, AP5. Nature, 319: 774–776. organization, and actin cytoskeleton at hippocampal CA3
https://doi.org/1038/319774a0 synapses. J Neurosci, 29: 10869–10882.
134. Norris CM, Foster TC, 1999, MK-801 improves retention in https://doi.org/1523/JNEUROSCI.5531-08.2009
aged rats: Implications for altered neural plasticity in age- 146. Brigman JL, Wright T, Talani G, et al., 2010, Loss of
related memory deficits. Neurobiol Learn Mem, 71: 194–206. GluN2B-containing NMDA receptors in CA1 hippocampus
https://doi.org/1006/nlme.1998.3864 and cortex impairs long-term depression, reduces
dendritic spine density, and disrupts learning. J Neurosci,
135. Villarreal DM, Do V, Haddad E, et al., NMDA receptor 30: 4590–4600.
antagonists sustain LTP and spatial memory: Active
processes mediate LTP decay. Nat Neurosci, 5: 48–52. https://doi.org/1523/JNEUROSCI.0640-10.2010
https://doi.org/1038/nn776 147. Von Engelhardt, J., Doganci B, Jensen V, et al., 2008,
Contribution of hippocampal and extra-hippocampal
136. Josselyn SA, Nguyen PV, 2005, CREB, synapses and memory NR2B-containing NMDA receptors to performance on
disorders: past progress and future challenges. Curr Drug spatial learning tasks. Neuron, 60: 846–860.
Targets CNS Neurol Disord, 4: 481–497.
https://doi.org/1016/j.neuron.2008.09.039(2008)
https://doi.org/2174/156800705774322058
148. Tang YP, Shimizu E, Dube GR, et al., 1999, Genetic
137. Malinow R, Malenka RC, 2002, AMPA receptor trafficking enhancement of learning and memory in mice. Nature,
and synaptic plasticity. Annu Rev Neurosci, 25: 103–126. 401: 63–69.
https://doi.org/1146/annurev.neuro.25.112701.142758 https://doi.org/1038/43432
138. Citri A, Malenka RC, 2008, Synaptic plasticity: multiple forms, 149. Zhou Y, Takahashi E, Li W, et al., 2007, Interactions between
functions, and mechanisms. Neuropsychopharmacology, the NR2B receptor and CaMKII modulate synaptic plasticity
33: 18–41. and spatial learning. J Neurosci, 27: 13843–13853.
https://doi.org/1038/sj.npp.1301559 https://doi.org/1523/JNEUROSCI.4486-07.2007
139. Malenka RC, 2003, Synaptic plasticity and AMPA receptor 150. Berberich S, Punnakkal P, Jensen V, et al., Lack of NMDA
trafficking. Ann N Y Acad Sci, 1003: 1–11. receptor subtype selectivity for hippocampal long-term
https://doi.org/1196/annals.1300.001 potentiation. J Neurosci, 25: 6907–6910.
140. Malenka RC, Bear MF, 2004, LTP and LTD: an https://doi.org/1523/JNEUROSCI.1905-05.2005
embarrassment of riches. Neuron, 44: 5–21. 151. Weitlauf C, Honse Y, Auberson YP, et al., 2005, Activation
https://doi.org/1016/j.neuron.2004.09.012 of NR2A-containing NMDA receptors is not obligatory
for NMDA receptor-dependent long-term potentiation.
141. Strack S, Colbran RJ, 1998, Autophosphorylation-dependent J Neurosci, 25: 8386–8390.
targeting of calcium/calmodulin-dependent protein kinase
II by the NR2B subunit of the N-methyl- D-aspartate https://doi.org/1523/JNEUROSCI.2388-05.2005
receptor. J Biol Chem, 273: 20689–20692. 152. Cui Z, Feng R, Jacobs S, et al., Increased NR2A: NR2B ratio
https://doi.org/1074/jbc.273.33.20689 compresses long-term depression range and constrains
long-term memory. Sci Rep, 3: 1036.
142. Barria A, Malinow R, 2005, NMDA receptor subunit
composition controls synaptic plasticity by regulating https://doi.org/1038/srep01036
binding to CaMKII. Neuron, 48: 289–301. 153. Hawasli AH, Benavides DR, Nguyen C, et al., 2007,
Volume 1 Issue 2 (2022) 21 https://doi.org/10.36922/an.v1i2.148

