The concentration of synaptically released glutamate outside of the climbing fiber-Purkinje cell synaptic cleft
Open accessAbstract
AMPA receptors and glutamate transporters expressed by cerebellar Bergmann glial cells are activated by neurotransmitter released from climbing fibers (Bergles et al., 1997). Based on anatomical evidence, this is most likely the result of glutamate diffusing out of the climbing fiber–Purkinje cell synaptic clefts (Palay and Chan-Palay, 1974). We used the change in the EC 50 of the Bergmann glia AMPA receptors produced by cyclothiazide (CTZ) to estimate the concentration of glutamate reached at the glial membrane. The decrease of the EC 50 gives rise to a concentration-dependent potentiation of the AMPA receptor-mediated responses (Patneau et al., 1993). By comparing the increase in amplitude of the AMPA receptor response in the Bergmann glia (840 ± 240%; n = 8) with the shift in the glutamate dose–response curve measured in excised patches (EC 50 , 1810 μ m in control vs 304 μ m in CTZ), we estimate that the extrasynaptic transmitter concentration reaches 160–190 μ m . This contrasts with the concentration in the synaptic cleft, thought to rapidly rise above 1 m m , but is still high enough to activate glutamate receptors. These results indicate that the sphere of influence of synaptically released glutamate can extend beyond the synaptic cleft.
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50 μM and 1 mM glutamate approximately represent extrasynaptic and active synaptic glutamate levels, respectively.
“Notably, 50 μM and 1 mM glutamate roughly estimate extrasynaptic and active synaptic glutamate levels, respectively”
From Mechanisms of ketamine and its metabolites as antidepressants (2022) · cites this paper as Dzubay & Jahr, 1999
The Abstract (p. 5265) says glutamate in the synaptic cleft is thought to rapidly rise above 1 mM, supporting 1 mM as a rough synaptic value. But it estimates the extrasynaptic peak at 160–190 μM, not 50 μM. (LLM, conf=0.90)
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Cites
A hippocampal GluR5 kainate receptor regulating inhibitory synaptic transmission
Clarke, V. R. J., Ballyk, B. A., Hoo, K. H., Mandelzys, A., Pellizzari, A., Bath, C. P., Thomas, J., Sharpe, E. F., Davies, C. H., Ornstein, P. L., et al. (1997) · Nature · doi:10.1038/39315 · Cited by 416 · see citing works
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Research works printed but not linked: 1
- Palay SL, Chan-Palay V (1974) The neuroglial cells of the cerebellar cortex and the climbing fiber. In: C erebellar cortex cytology and orga- nization (Palay SL, Chan-Palay V, eds), pp 288 -321. New York: Springer.
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Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686 · see citing works
A neuron–glia signalling network in the active brain
Bezzi, P., & Volterra, A. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00223-3 · Cited by 446 · see citing works
Extracellular glutamate: functional compartments operate in different concentration ranges
Moussawi, K., Riegel, A., Nair, S., & Kalivas, P. W. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00094 · Cited by 184 · see citing works
Mechanisms of ketamine and its metabolites as antidepressants
Hess, E. M., Riggs, L. M., Michaelides, M., & Gould, T. D. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114892 · Cited by 169 · see citing works
Ectopic Release of Synaptic Vesicles
Matsui, K., & Jahr, C. E. (2003) · Neuron · doi:10.1016/s0896-6273(03)00788-8 · Cited by 155 · see citing works
Self-citationGlutamate mediates acute glucose transport inhibition in hippocampal neurons
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- Authors
- Dzubay, J. A., & Jahr, C. E.
- Affiliations
- Oregon Health & Science University (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1999-07-01
- Volume
- 19
- Issue
- 13
- Pages
- 5265-5274
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6782308
- OpenAlex
- W2132949150
- Cited by
- 213
- References
- 1
- Citations by year
- 2026: 6 · 2025: 5 · 2024: 6 · 2023: 7 · 2022: 8 · 2021: 14 · 2020: 6 · 2019: 5 · 2018: 4 · 2017: 2 · 2016: 7 · 2015: 10 · 2014: 6 · 2013: 3 · 2012: 8
- FWCI
- 4.82
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (1f31mh011978-01)
- National Institute of Mental Health (MH11978)
- National Institute of Neurological Disorders and Stroke (NS-21419, R01NS021419)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- extrasynaptic glutamate, Bergmann glia, AMPA receptors, glutamate transporters, cyclothiazide, glutamate diffusion, synaptic cleft, cerebellum, receptor potentiation
- MeSH terms
- Animals, Benzothiadiazines, Cell Membrane, Dose-Response Relationship, Drug, Kinetics, Models, Biological, Neuroglia, Probability, Purkinje Cells, Quinoxalines, Synapses, Temperature, Receptors, AMPA, Patch-Clamp Techniques, ATP-Binding Cassette Transporters, Glutamic Acid, Amino Acid Transport System X-AG, Rats, In Vitro Techniques
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