Distribution of extracellular glutamate in the neuropil of hippocampus.

Reported values of extracellular glutamate concentrations in the resting state depend on the method of measurement and vary ∼1000-fold. As glutamate levels in the micromolar range can cause receptor desensitization and excitotoxicity, and thus affect neuronal excitability, an accurate determination...

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Main Authors: Melissa A Herman, Ben Nahir, Craig E Jahr
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3206024?pdf=render
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spelling doaj-7c97d9cfc7ff46a7b5c0479cb9877a8c2020-11-25T01:21:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01611e2650110.1371/journal.pone.0026501Distribution of extracellular glutamate in the neuropil of hippocampus.Melissa A HermanBen NahirCraig E JahrReported values of extracellular glutamate concentrations in the resting state depend on the method of measurement and vary ∼1000-fold. As glutamate levels in the micromolar range can cause receptor desensitization and excitotoxicity, and thus affect neuronal excitability, an accurate determination of ambient glutamate is important. Part of the variability of previous measurements may have resulted from the sampling of glutamate in different extracellular compartments, e.g., synaptic versus extrasynaptic volumes. A steep concentration gradient of glutamate between these two compartments could be maintained, for example, by high densities of glutamate transporters arrayed at the edges of synapses. We have used two photon laser scanning microscopy and electrophysiology to investigate whether extracellular glutamate is compartmentalized in acute hippocampal slices. Pharmacological blockade of NMDARs had no effect on Ca(2+) transients generated in dendritic shafts or spines of CA1 pyramidal neurons by depolarization, suggesting that ambient glutamate is too low to activate a significant number of NMDARs. Furthermore, blockade of transporters did not flood the synapse with glutamate, indicating that synaptic NMDARs are not protected from high concentrations of extrasynaptic glutamate. We suggest that, in the CA1 region of hippocampus, glutamate transporters do not create a privileged space within the synapse but rather keep ambient glutamate at very low levels throughout the neuropil.http://europepmc.org/articles/PMC3206024?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Melissa A Herman
Ben Nahir
Craig E Jahr
spellingShingle Melissa A Herman
Ben Nahir
Craig E Jahr
Distribution of extracellular glutamate in the neuropil of hippocampus.
PLoS ONE
author_facet Melissa A Herman
Ben Nahir
Craig E Jahr
author_sort Melissa A Herman
title Distribution of extracellular glutamate in the neuropil of hippocampus.
title_short Distribution of extracellular glutamate in the neuropil of hippocampus.
title_full Distribution of extracellular glutamate in the neuropil of hippocampus.
title_fullStr Distribution of extracellular glutamate in the neuropil of hippocampus.
title_full_unstemmed Distribution of extracellular glutamate in the neuropil of hippocampus.
title_sort distribution of extracellular glutamate in the neuropil of hippocampus.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Reported values of extracellular glutamate concentrations in the resting state depend on the method of measurement and vary ∼1000-fold. As glutamate levels in the micromolar range can cause receptor desensitization and excitotoxicity, and thus affect neuronal excitability, an accurate determination of ambient glutamate is important. Part of the variability of previous measurements may have resulted from the sampling of glutamate in different extracellular compartments, e.g., synaptic versus extrasynaptic volumes. A steep concentration gradient of glutamate between these two compartments could be maintained, for example, by high densities of glutamate transporters arrayed at the edges of synapses. We have used two photon laser scanning microscopy and electrophysiology to investigate whether extracellular glutamate is compartmentalized in acute hippocampal slices. Pharmacological blockade of NMDARs had no effect on Ca(2+) transients generated in dendritic shafts or spines of CA1 pyramidal neurons by depolarization, suggesting that ambient glutamate is too low to activate a significant number of NMDARs. Furthermore, blockade of transporters did not flood the synapse with glutamate, indicating that synaptic NMDARs are not protected from high concentrations of extrasynaptic glutamate. We suggest that, in the CA1 region of hippocampus, glutamate transporters do not create a privileged space within the synapse but rather keep ambient glutamate at very low levels throughout the neuropil.
url http://europepmc.org/articles/PMC3206024?pdf=render
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AT bennahir distributionofextracellularglutamateintheneuropilofhippocampus
AT craigejahr distributionofextracellularglutamateintheneuropilofhippocampus
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