The DOI matches its Crossref record; 68 of the 68 references it cites were found in a registry or an index.
Parvalbumin, somatostatin and cholecystokinin as chemical markers for specific GABAergic interneuron types in the rat frontal cortex
Abstract
It remains to be clarified how many classes of GABAergic nonpyramidal cells exist in the cortical circuit. We have divided GABA cells in the rat frontal cortex into 3 groups, based on their firing characteristics: fast-spiking (FS) cells, late-spiking (LS) cells, and non-FS cells. Expression of calcium-binding proteins and peptides could be shown in separate groups of GABA cells in layers II/III and V of the frontal cortex: (1) parvalbumin cells, (2) somatostatin cells, (3) calretinin and/or vasoactive intestinal polypeptide (VIP) cells [partially positive for cholecystokinin (CCK)] and (4) large CCK cells (almost negative for VIP/calretinin). Combining the physiological and chemical properties of morphologically diverse nonpyramidal cells allows division into several groups, including FS basket cells containing parvalbumin, non-FS somatostatin Martinotti cells with ascending axonal arbors, and non-FS large basket cells positive for CCK. These subtypes show characteristic spatial distributions of axon collaterals and the innervation tendency of postsynaptic elements. With synchronized activity induced by cortical excitatory or inhibitory circuits, firing patterns were also found to differ. Subtype-selective occurrence of electrical coupling, finding for potassium channel Kv3.1 proteins, and cholinergic and serotonergic modulation supports our tentative classification. To clarify the functional architecture in the frontal cortex, it is important to reveal the connectional characteristics of GABA cell subtypes and determine whether they are similar to those in other cortical regions.
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“On the other hand, O-LMs express PV, albeit at significantly lower levels than AACs/PVBCs/BiCs, while PV and SST are considered mutually exclusive in the neocortex (324, 344, 561, 568, 582, 721, 1142, 1237).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [568]
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Research works printed but not linked: 2
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NEURONAL CIRCUITS OF THE NEOCORTEX
Douglas, R. J., & Martin, K. A. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144152 · Cited by 1,886
How Inhibition Shapes Cortical Activity
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Reconstruction and Simulation of Neocortical Microcircuitry
Markram, H., Muller, E., Ramaswamy, S., Reimann, M. W., Abdellah, M., Sanchez, C. A., Ailamaki, A., Alonso-Nanclares, L., Antille, N., Arsever, S., et al. (2015) · Cell · doi:10.1016/j.cell.2015.09.029 · Cited by 1,557
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889
Metadata
- Authors
- Kawaguchi, Y., & Kondo, S.
- Affiliations
- National Institute for Physiological Sciences (JP)
- Corresponding author
- Kawaguchi, Yasuo
- ORCID
- Kawaguchi, Yasuo
- Venue
- Journal of Neurocytology
- Published
- 2002-03
- Volume
- 31
- Issue
- 3-5
- Pages
- 277-287
- ISSN
- 0300-4864 (ISSN-L)
- 1573-7381
- OpenAlex
- W1923448222
- Cited by
- 395
- References
- 68
- Citations by year
- 2026: 1 · 2025: 8 · 2024: 12 · 2023: 15 · 2022: 7 · 2021: 11 · 2020: 17 · 2019: 13 · 2018: 14 · 2017: 14 · 2016: 13 · 2015: 22 · 2014: 13 · 2013: 31 · 2012: 28
- FWCI
- 3.25
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Neurocytology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- parvalbumin, somatostatin, cholecystokinin, GABAergic interneurons, frontal cortex, basket cells, Martinotti cells, calcium-binding proteins, calretinin, vasoactive intestinal peptide, Kv3.1 potassium channel, electrical coupling, cholinergic modulation, serotonergic modulation, axon collaterals
- MeSH terms
- Action Potentials, Animals, Cholecystokinin, Frontal Lobe, gamma-Aminobutyric Acid, Image Processing, Computer-Assisted, Interneurons, Parvalbumins, Somatostatin, Presynaptic Terminals, Rats
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