Literature DB >> 9875351

Subcellular and subsynaptic distribution of the NR1 subunit of the NMDA receptor in the neostriatum and globus pallidus of the rat: co-localization at synapses with the GluR2/3 subunit of the AMPA receptor.

V Bernard1, J P Bolam.   

Abstract

Glutamatergic neurotransmission in the neostriatum and the globus pallidus is mediated through NMDA-type as well as other glutamate receptors and is critical in the expression of basal ganglia function. In order to characterize the cellular, subcellular and subsynaptic localization of NMDA receptors in the neostriatum and globus pallidus, multiple immunocytochemical techniques were applied using antibodies that recognize the NR1 subunit of the NMDA receptor. In order to determine the spatial relationship between NMDA receptors and AMPA receptors, double labelling was performed with the NR1 antibodies and an antibody that recognizes the GluR2 and 3 subunits of the AMPA receptor. In the neostriatum all neurons with characteristics of spiny projection neurons, some interneurons and many dendrites and spines were immunoreactive for NR1. In the globus pallidus most perikarya and many dendritic processes were immunopositive. Immunogold methods revealed that most NR1 labelling is associated with asymmetrical synapses and, like the labelling for GluR2/3, is evenly spread across the synapse. Double immunolabelling revealed that in neostriatum, over 80% of NR1-positive axospinous synapses are also positive for GluR2/3. In the globus pallidus most NR1-positive synapses are positive for GluR2/3. In both regions many synapses labelled only for GluR2/3 were also detected. These results, together with previous data, suggest that NMDA and AMPA receptor subunits are expressed by the same neurons in the neostriatum and globus pallidus and that NMDA and AMPA receptors are, at least in part, colocalized at individual asymmetrical synapses. The synaptic responses to glutamate in these regions are thus likely be mediated by both AMPA and NMDA receptors at the level of individual synapses.

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Year:  1998        PMID: 9875351     DOI: 10.1046/j.1460-9568.1998.00380.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  40 in total

1.  Regulation of the subcellular distribution of m4 muscarinic acetylcholine receptors in striatal neurons in vivo by the cholinergic environment: evidence for regulation of cell surface receptors by endogenous and exogenous stimulation.

Authors:  V Bernard; A I Levey; B Bloch
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Organization of ionotropic glutamate receptors at dendrodendritic synapses in the rat olfactory bulb.

Authors:  M Sassoè-Pognetto; O P Ottersen
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

3.  NMDA receptor content of synapses in stratum radiatum of the hippocampal CA1 area.

Authors:  C Racca; F A Stephenson; P Streit; J D Roberts; P Somogyi
Journal:  J Neurosci       Date:  2000-04-01       Impact factor: 6.167

Review 4.  Synaptic organisation of the basal ganglia.

Authors:  J P Bolam; J J Hanley; P A Booth; M D Bevan
Journal:  J Anat       Date:  2000-05       Impact factor: 2.610

5.  Dendritic calcium encodes striatal neuron output during up-states.

Authors:  Jason N D Kerr; Dietmar Plenz
Journal:  J Neurosci       Date:  2002-03-01       Impact factor: 6.167

6.  PSD-95 family MAGUKs are essential for anchoring AMPA and NMDA receptor complexes at the postsynaptic density.

Authors:  Xiaobing Chen; Jonathan M Levy; Austin Hou; Christine Winters; Rita Azzam; Alioscka A Sousa; Richard D Leapman; Roger A Nicoll; Thomas S Reese
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-24       Impact factor: 11.205

Review 7.  The external globus pallidus: progress and perspectives.

Authors:  Daniel J Hegeman; Ellie S Hong; Vivian M Hernández; C Savio Chan
Journal:  Eur J Neurosci       Date:  2016-03-28       Impact factor: 3.386

8.  Laminar organization of the NMDA receptor complex within the postsynaptic density.

Authors:  J G Valtschanoff; R J Weinberg
Journal:  J Neurosci       Date:  2001-02-15       Impact factor: 6.167

9.  Inhibition of striatal dopamine release by CB1 receptor activation requires nonsynaptic communication involving GABA, H2O2, and KATP channels.

Authors:  Zsuzsanna Sidló; Patricia H Reggio; Margaret E Rice
Journal:  Neurochem Int       Date:  2007-07-22       Impact factor: 3.921

Review 10.  Classification of H₂O₂as a neuromodulator that regulates striatal dopamine release on a subsecond time scale.

Authors:  Jyoti C Patel; Margaret E Rice
Journal:  ACS Chem Neurosci       Date:  2012-11-08       Impact factor: 4.418

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