The DOI matches its Crossref record; 48 of the 49 references it cites were found in a registry or an index.
Different transmitter transients underlie presynaptic cell type specificity of GABA A,slow and GABA A,fast
Open accessAbstract
Phasic (synaptic) and tonic (extrasynaptic) inhibition represent the two most fundamental forms of GABA(A) receptor-mediated transmission. Inhibitory postsynaptic currents (IPSCs) generated by GABA(A) receptors are typically extremely rapid synaptic events that do not last beyond a few milliseconds. Although unusually slow GABA(A) IPSCs, lasting for tens of milliseconds, have been observed in recordings of spontaneous events, their origin and mechanisms are not known. We show that neocortical GABA(A,slow) IPSCs originate from a specialized interneuron called neurogliaform cells. Compared with classical GABA(A,fast) IPSCs evoked by basket cells, single spikes in neurogliaform cells evoke extraordinarily prolonged GABA(A) responses that display tight regulation by transporters, low peak GABA concentration, unusual benzodiazepine modulation, and spillover. These results reveal a form of GABA(A) receptor mediated communication by a dedicated cell type that produces slow ionotropic responses with properties intermediate between phasic and tonic inhibition.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“These features combined with the dense local ramification of NGFC axons are considered to underlie the ability of NGFCs to mediate volume transmission leading to slow dual component (GABAAR- and GABABR-mediated) inhibition at virtually any postsynaptic element within their dense axonal plexus (550, 926, 927, 1074, 1086).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1074]
In the citing paper
“While neocortical NGFCs can be found throughout all layers, they are particularly enriched in supragranular layers and form a major constituent cell population in L1 (564, 858, 1017, 1074, 1086, 1134).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1074]
In the citing paper
“Of particular interest, in contrast to the rapid and synchronous IPSCs produced by PVBCs, transmission from NGFCs generates long-lasting IPSCs resulting from prolonged GABA transients (550, 1074, 1086) that arise from the unusual synaptic architecture where bouton density is high but close apposition to specialized postsynaptic densities is low (550, 751, 858, 1074) (FIGURE 13C).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1074]
In the citing paper
“Electrophysiological recordings from pairs of NGFCs demonstrate a marked functional connectivity with each other (48, 550, 926, 1074).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1074]
In the citing paper
“These remarkably slow kinetics are not fully attributable to dendritic filtering, asynchronous release, spillover, nor the properties of the GABAARs themselves (however, see Refs. 483, 1264) but are primarily due to the spatiotemporal profile of GABA release from this interneuron subtype (see sect. IVL) (167, 550, 870, 1074).”
From Hippocampal GABAergic Inhibitory Interneurons (2017) · cites this paper as [1074]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Variations on an inhibitory theme: phasic and tonic activation of GABAA receptors
Farrant, M., & Nusser, Z. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1625 · Cited by 2,081
Nusser, Z., Sieghart, W., & Somogyi, P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-05-01693.1998 · Cited by 835
Stell, B. M., Brickley, S. G., Tang, C., Farrant, M., & Módy, I. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2435457100 · Cited by 799
Tonically active GABAA receptors: modulating gain and maintaining the tone
Semyanov, A. V., Walker, M. C., Kullmann, D. M., & Silver, R. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.03.005 · Cited by 757
Brickley, S. G., Cull-Candy, S. G., & Farrant, M. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021806 · Cited by 717
Shunting Inhibition Modulates Neuronal Gain during Synaptic Excitation
Mitchell, S. J., & Silver, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00200-9 · Cited by 602
Desensitized states prolong GABAA channel responses to brief agonist pulses
Jones, M. V., & Westbrook, G. L. (1995) · Neuron · doi:10.1016/0896-6273(95)90075-6 · Cited by 584
Hefft, S., & Jonas, P. (2005) · Nature Neuroscience · doi:10.1038/nn1542 · Cited by 583
Caraiscos, V. B., Elliott, E. M., You-Ten, K. E., Cheng, V., Belelli, D., Newell, J. G., Jackson, M. F., Lambert, J. J., Rosahl, T. W., Wafford, K. A., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307231101 · Cited by 571
Diversity of inhibitory neurotransmission through GABAA receptors
Módy, I., & Pearce, R. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.07.002 · Cited by 532
Cited by
Sorted by citations
GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations
Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050
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
Extrasynaptic GABAA Receptors: Their Function in the CNS and Implications for Disease
Brickley, S. G., & Módy, I. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.012 · Cited by 695
Regulation of cortical microcircuits by unitary GABA-mediated volume transmission
Oláh, S., Füle, M., Komlósi, G., Varga, C., Báldi, R., Barzó, P., & Tamás, G. (2009) · Nature · doi:10.1038/nature08503 · Cited by 386
Self-citationThe organization of two new cortical interneuronal circuits
Jiang, X., Wang, G., Lee, A. J., Stornetta, R. L., & Zhu, J. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3305 · Cited by 338
Olmos-Serrano, J. L., Paluszkiewicz, S. M., Martin, B. S., Kaufmann, W. E., Corbin, J. G., & Huntsman, M. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1714-10.2010 · Cited by 309
Billeh, Y. N., Cai, B., Gratiy, S. L., Dai, K., Iyer, R., Gouwens, N. W., Abbasi-Asl, R., Jia, X., Siegle, J. H., Olsen, S. R., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.01.040 · Cited by 320
GABAergic circuits mediate the reinforcement-related signals of striatal cholinergic interneurons
English, D. F., Ibáñez-Sandoval, O., Stark, E., Tecuapetla, F., Buzsáki, G., Deisseroth, K. A., Tepper, J. M., & Koós, T. Z. (2011) · Nature Neuroscience · doi:10.1038/nn.2984 · Cited by 312
Fuentealba, P., Begum, R., Capogna, M., Jinno, S., Márton, L. F., Csicsvari, J., Thomson, A., Somogyi, P., & Klausberger, T. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.034 · Cited by 255
Classification of NPY-Expressing Neocortical Interneurons
Karagiannis, A., Gallopin, T., Dávid, C., Battaglia, D., Geoffroy, H., Rossier, J., Hillman, E. M. C., Staiger, J. F., & Cauli, B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0058-09.2009 · Cited by 256
Structure, function, and plasticity of GABA transporters
Scimemi, A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00161 · Cited by 261
GABA Neuron Alterations, Cortical Circuit Dysfunction and Cognitive Deficits in Schizophrenia
González‐Burgos, G., Fish, K. N., & Lewis, D. A. (2011) · Neural Plasticity · doi:10.1155/2011/723184 · Cited by 250
A blanket of inhibition: functional inferences from dense inhibitory connectivity
Karnani, M. M., Agetsuma, M., & Yuste, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.015 · Cited by 188
Bezaire, M. J., Raikov, I., Burk, K., Vyas, D., & Soltesz, I. (2016) · eLife · doi:10.7554/elife.18566 · Cited by 198
Inhibitory Control of Prefrontal Cortex by the Claustrum
Jackson, J., Karnani, M., Zemelman, B. V., Burdakov, D., & Lee, A. K. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.031 · Cited by 197
Four Unique Interneuron Populations Reside in Neocortical Layer 1
Schuman, B., Machold, R. P., Hashikawa, Y., Fuzik, J., Fishell, G. J., & Rudy, B. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1613-18.2018 · Cited by 184
“Indeed, this phenomenon may explain their high connection probability to most cell types (Szabadics et al., 2007).”
BackgroundResultInfluentialNon‐synaptic receptors and transporters involved in brain functions and targets of drug treatment
Vizi, E. S., Fekete, Á., Károly, R., & Mike, Á. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00624.x · Cited by 193
Common Origins of Hippocampal Ivy and Nitric Oxide Synthase Expressing Neurogliaform Cells
Tricoire, L., Pelkey, K. A., Daw, M. I., Sousa, V. H., Miyoshi, G., Jeffries, B., Cauli, B., Fishell, G., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5123-09.2010 · Cited by 171
Structured dendritic inhibition supports branch-selective integration in CA1 pyramidal cells
Bloss, E. B., Cembrowski, M. S., Karsh, B., Colonell, J., Fetter, R. D., & Spruston, N. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.029 · Cited by 164
Neurogliaform cells in cortical circuits
Overstreet-Wadiche, L., & McBain, C. J. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3969 · Cited by 152
A Novel Functionally Distinct Subtype of Striatal Neuropeptide Y Interneuron
Ibáñez-Sandoval, O., Tecuapetla, F., Ünal, B., Shah, F., Koós, T. Z., & Tepper, J. M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2628-11.2011 · Cited by 150
Determining the Neurotransmitter Concentration Profile at Active Synapses
Scimemi, A., & Beato, M. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8087-7 · Cited by 151
Hippocampal GABAergic interneurons and memory
Tzilivaki, A., Tukker, J. J., Maier, N., Poirazi, P., Sammons, R. P., & Schmitz, D. (2023) · Neuron · doi:10.1016/j.neuron.2023.06.016 · Cited by 154
Wozny, C., & Williams, S. R. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq257 · Cited by 129
Inhibitory Interneurons and their Circuit Motifs in the Many Layers of the Barrel Cortex
Feldmeyer, D., Qi, G., Emmenegger, V., & Staiger, J. F. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.027 · Cited by 140
Noninvasive Stimulation of the Human Brain: Activation of Multiple Cortical Circuits
Lazzaro, V. D., Rothwell, J. C., & Capogna, M. (2017) · The Neuroscientist · doi:10.1177/1073858417717660 · Cited by 136
GABAA,slow: causes and consequences
Capogna, M., & Pearce, R. A. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2010.10.005 · Cited by 129
Postnatal Switch from Synaptic to Extrasynaptic Transmission between Interneurons and NG2 Cells
Vélez‐Fort, M., Maldonado, P. P., Butt, A. M., Audinat, É., & Angulo, M. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0238-10.2010 · Cited by 127
GABAB Receptor Modulation of Feedforward Inhibition through Hippocampal Neurogliaform Cells
Price, C. J., Scott, R., Rusakov, D. A., & Capogna, M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4673-07.2008 · Cited by 107
Cortical Oscillations in Health and Disease
Traub, R. D., & Whittington, M. A. (2010) · doi:10.1093/acprof:oso/9780195342796.001.0001 · Cited by 108
Interneuron networks in the hippocampus
Kullmann, D. M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.05.006 · Cited by 119
Inhibitory interneurons in visual cortical plasticity
van Versendaal, D., & Levelt, C. N. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2264-4 · Cited by 113
GABA A Receptor α5 Subunits Contribute to GABA A,slow Synaptic Inhibition in Mouse Hippocampus
Żarnowska, E. D., Keist, R., Rudolph, U., & Pearce, R. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.91203.2008 · Cited by 105
Functional Specificity of Mossy Fiber Innervation of GABAergic Cells in the Hippocampus
Szabadics, J., & Soltész, I. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5390-08.2009 · Cited by 98
Self-citationInput-Specific GABAergic Signaling to Newborn Neurons in Adult Dentate Gyrus
Markwardt, S. J., Wadiche, J. I., & Overstreet‐Wadiche, L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2727-09.2009 · Cited by 102
Unitary inhibitory field potentials in the CA3 region of rat hippocampus
Bazelot, M., Dinocourt, C., Cohen, I., & Miles, R. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2009.185918 · Cited by 101
Lee, A. J., Wang, G., Jiang, X., Johnson, S. M., Hoang, E. T., Lanté, F., Stornetta, R. L., Beenhakker, M. P., Shen, Y., & Julius Zhu, J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu020 · Cited by 94
Noradrenergic Modulation of Electrical Coupling in GABAergic Networks of the Hippocampus
Zsiros, V., & Maccaferri, G. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4616-07.2008 · Cited by 93
Capogna, M. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.201004 · Cited by 91
Differential processing of thalamic information via distinct striatal interneuron circuits
Assous, M., Kaminer, J., Shah, F., Garg, A., Koós, T. Z., & Tepper, J. M. (2017) · Nature Communications · doi:10.1038/ncomms15860 · Cited by 89
Neurogliaform and Ivy Cells: A Major Family of nNOS Expressing GABAergic Neurons
Armstrong, C., Krook-Magnuson, E., & Soltesz, I. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00023 · Cited by 88
Perisomatic inhibition and cortical circuit dysfunction in schizophrenia
Lewis, D. A., Fish, K. N., Arion, D., & Gonzalez-Burgos, G. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.05.013 · Cited by 87
Armstrong, C., Szabadics, J., Tamás, G., & Soltesz, I. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22577 · Cited by 86
Self-citationIvy and Neurogliaform Interneurons Are a Major Target of μ-Opioid Receptor Modulation
Krook-Magnuson, E., Luu, L., Lee, S.-H., Varga, C., & Soltesz, I. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2269-11.2011 · Cited by 75
Karayannis, T., Elfant, D., Huerta-Ocampo, I., Teki, S., Scott, R. S., Rusakov, D. A., Jones, M. V., & Capogna, M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5883-09.2010 · Cited by 85
Herd, M. B., Brown, A. R., Lambert, J. J., & Belelli, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1174-13.2013 · Cited by 85
Ivy/neurogliaform interneurons coordinate activity in the neurogenic niche
Markwardt, S. J., Dieni, C. V., Wadiche, J. I., & Overstreet-Wadiche, L. (2011) · Nature Neuroscience · doi:10.1038/nn.2935 · Cited by 82
Davenport, E. C., Pendolino, V., Kontou, G., McGee, T. P., Sheehan, D. F., López‐Doménech, G., Farrant, M., & Kittler, J. T. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.025 · Cited by 80
Neurogliaform cells dynamically regulate somatosensory integration via synapse-specific modulation
Chittajallu, R., Pelkey, K. A., & McBain, C. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3284 · Cited by 73
Crowley, J. J., Fioravante, D., & Regehr, W. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.004 · Cited by 74
Phasic, Nonsynaptic GABA-A Receptor-Mediated Inhibition Entrains Thalamocortical Oscillations
Rovó, Z., Mátyás, F., Barthó, P., Slézia, A., Lecci, S., Pellegrini, C., Astori, S., Dávid, C., Hangya, B., Lüthi, A., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4386-13.2014 · Cited by 71
Hartwich, K., Pollak, T., & Klausberger, T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1397-09.2009 · Cited by 74
Synaptic and cellular organization of layer 1 of the developing rat somatosensory cortex
Muralidhar, S., Wang, Y., & Markram, H. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00052 · Cited by 71
Sleep down state-active ID2/Nkx2.1 interneurons in the neocortex
Valero, M., Viney, T. J., Machold, R. P., Mederos, S., Zutshi, I., Schuman, B., Senzai, Y., Rudy, B., & Buzsáki, G. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00797-6 · Cited by 64
New dimensions of interneuronal specialization unmasked by principal cell heterogeneity
Krook-Magnuson, E., Varga, C., Lee, S.-H., & Soltesz, I. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.005 · Cited by 63
Dynamic functions of GABA signaling during granule cell maturation
Dieni, C. V., Chancey, J. H., & Overstreet‐Wadiche, L. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00113 · Cited by 64
In Vitro Recordings of Human Neocortical Oscillations
Florez, C. M., McGinn, R. J., Lukankin, V., Marwa, I., Sugumar, S., Dian, J. A., Hazrati, L., Carlen, P. L., Zhang, L., & Valiante, T. A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht235 · Cited by 62
Barberis, A., Petrini, E. M., & Mozrzymas, J. W. (2011) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2011.00006 · Cited by 64
Courtney, N. A., & Ford, C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0166-14.2014 · Cited by 63
Assortment of GABAergic Plasticity in the Cortical Interneuron Melting Pot
Méndez, P., & Bacci, A. (2011) · Neural Plasticity · doi:10.1155/2011/976856 · Cited by 61
Mechanisms of 5‐HT 1A receptor‐mediated transmission in dorsal raphe serotonin neurons
Courtney, N. A., & Ford, C. (2015) · The Journal of Physiology · doi:10.1113/jp271716 · Cited by 55
Beyond the frontiers of neuronal types
Battaglia, D. A., Karagiannis, A., Gallopin, T., Gutch, H. W., & Cauli, B. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00013 · Cited by 61
Medalla, M., Gilman, J. P., Wang, J., & Luebke, J. I. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3757-16.2017 · Cited by 56
Łątka, K., Jończyk, J., & Bajda, M. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.04.126 · Cited by 53
Vargas‐Caballero, M., Martin, L. J., Salter, M. W., Orser, B. A., & Paulsen, O. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.11.005 · Cited by 52
Neurogliaform cells of amygdala: a source of slow phasic inhibition in the basolateral complex
Mańko, M., Bienvenu, T. C. M., Dalezios, Y., & Capogna, M. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.236745 · Cited by 51
Interneuronal GABAA receptors inside and outside of synapses
Ferando, I., & Módy, I. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.001 · Cited by 50
González‐Burgos, G., Rotaru, D. C., Zaitsev, A. V., Povysheva, N. V., & Lewis, D. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.91161.2008 · Cited by 49
Jiménez-González, C., Pirttimäki, T., Cope, D. W., & Parri, H. R. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07645.x · Cited by 47
GABA Transporter GAT1: A Crucial Determinant of GABAB Receptor Activation in Cortical Circuits?
Gonzalez-Burgos, G. (2010) · Advances in Pharmacology · doi:10.1016/s1054-3589(10)58008-6 · Cited by 38
Altered GABAA,slowInhibition and Network Oscillations in Mice Lacking the GABAAReceptor β3Subunit
Hentschke, H., Benkwitz, C., Banks, M. I., Perkins, M. G., Homanics, G. E., & Pearce, R. A. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00651.2009 · Cited by 43
Kobayashi, M., Hamada, T., Kogo, M., Yanagawa, Y., Obata, K., & Kang, Y. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06401.x · Cited by 43
Li, P., Rudolph, U., & Huntsman, M. M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900922106 · Cited by 38
Extrasynaptic δ-subunit containing GABAA receptors
Arslan, A. (2021) · Journal of Integrative Neuroscience · doi:10.31083/j.jin.2021.01.284 · Cited by 36
Varga, C., Tamás, G., Barzó, P., Oláh, S., & Somogyi, P. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv045 · Cited by 34
Self-citationNeurogliaform cells dynamically decouple neuronal synchrony between brain areas
Sakalar, E., Klausberger, T., & Lasztóczi, B. (2022) · Science · doi:10.1126/science.abo3355 · Cited by 34
Quattrocolo, G., & Maccaferri, G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5680-12.2013 · Cited by 34
Synaptic mechanisms of top-down control in the non-lemniscal inferior colliculus
Oberle, H. M., Ford, A. N., Dileepkumar, D., Czarny, J., & Apostolides, P. F. (2021) · eLife · doi:10.7554/elife.72730 · Cited by 36
Connelly, W. M., & Lees, G. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2009.185199 · Cited by 29
Parvalbumin interneurons provide spillover to newborn and mature dentate granule cells
Vaden, R. J., Gonzalez, J., Tsai, M., Niver, A. J., Fusilier, A. R., Griffith, C. M., Krämer, R., Wadiche, J. I., & Overstreet‐Wadiche, L. (2020) · eLife · doi:10.7554/elife.54125 · Cited by 30
Labrakakis, C., Rudolph, U., & Koninck, Y. D. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00424 · Cited by 28
Ye, Z., McGee, T. P., Houston, C. M., & Brickley, S. G. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00203 · Cited by 28
Two GABAA responses with distinct kinetics in a sound localization circuit
Tang, Z., & Lu, Y. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.230136 · Cited by 26
Morphology of Hippocampal Neurons
Vida, I. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0996-1_2 · Cited by 30
The neuronal identity bias behind neocortical GABAergic plasticity
Allène, C., Lourenço, J., & Bacci, A. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.008 · Cited by 29
Inhibition and oscillations in the human brain tissue in vitro
de la Prida, L. M., & Huberfeld, G. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.02.006 · Cited by 21
Amnestic Concentrations of Etomidate Modulate GABAA,slowSynaptic Inhibition in Hippocampus
Dai, S., Perouansky, M. A., & Pearce, R. A. (2009) · Anesthesiology · doi:10.1097/aln.0b013e3181b4392d · Cited by 21
Lawrence, J. J., Haario, H., & Stone, E. F. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00167.2014 · Cited by 19
Anstötz, M., Quattrocolo, G., & Maccaferri, G. (2018) · Brain Research · doi:10.1016/j.brainres.2018.07.028 · Cited by 19
Kecskés, M., Henn-Mike, N., Agócs-Laboda, Á., Szőcs, S., Petykó, Z., & Varga, C. (2020) · Communications Biology · doi:10.1038/s42003-020-01496-x · Cited by 18
Activity-dependent modulation of inhibitory synaptic kinetics in the cochlear nucleus
Nerlich, J., Keine, C., Ruebsamen, R., Burger, R. M., & Milenković, I. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00145 · Cited by 20
Cell Type-specific Intrinsic Perithreshold Oscillations in Hippocampal GABAergic Interneurons
Kang, Y., Lewis, H. E. S., Young, M. W., Govindaiah, G., Greenfield, L. J., García‐Rill, E., & Lee, S.-H. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.02.014 · Cited by 16
Somogyi, J., Szabo, A., Somogyi, P., & Lamsa, K. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00035 · Cited by 17
Transcriptomic cell-type specificity of local cortical circuits
Patiño, M., Rossa, M., Lagos, W. N., Patne, N. S., & Callaway, E. M. (2024) · Neuron · doi:10.1016/j.neuron.2024.09.003 · Cited by 19
Ammer, J. J., Siveke, I., & Felmy, F. (2015) · Current Biology · doi:10.1016/j.cub.2015.04.026 · Cited by 17
The Role of Regulatory Transporters in Neuropathic Pain
Yousuf, M. S., & Kerr, B. J. (2016) · Advances in pharmacology · doi:10.1016/bs.apha.2015.12.003 · Cited by 19
Functional properties of GABA synaptic inputs onto GABA neurons in monkey prefrontal cortex
Rotaru, D. C., Olezene, C. S., Miyamae, T., Povysheva, N. V., Zaitsev, A. V., Lewis, D. A., & González‐Burgos, G. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00799.2014 · Cited by 15
Song, C., Kang, X., Yang, F., Du, W., Zhang, J., Liu, L., Kang, J., Jia, N., Yue, H., Fan, L., et al. (2021) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0134 · Cited by 15
Khamma, J. K., Copeland, D. S., Hake, H. S., & Gantz, S. C. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1176-21.2021 · Cited by 16
Metadata
- Authors
- Szabadics, J., Tamás, G., & Soltesz, I.
- Affiliations
- University of California, Irvine (US)
- University of Szeged (HU)
- *Department of Anatomy and Neurobiology, University of California, 193 Irvine Hall, Irvine, CA 92697; and
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-09-11
- Volume
- 104
- Issue
- 37
- Pages
- 14831-14836
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1964542
- OpenAlex
- W2004000308
- Cited by
- 170
- References
- 49
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 5 · 2023: 2 · 2022: 2 · 2021: 9 · 2020: 8 · 2019: 3 · 2018: 9 · 2017: 6 · 2016: 7 · 2015: 6 · 2014: 14 · 2013: 9 · 2012: 8
- FWCI
- 7.41
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- National Institute of Neurological Disorders and Stroke (R29NS035915, R01NS035915, NS-35915, R37NS035915)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- GABAA receptor, tonic inhibition, extrasynaptic inhibition, phasic inhibition, neurogliaform cells, basket cells, inhibitory postsynaptic currents, benzodiazepine modulation, GABA transporters, neocortex, interneurons, presynaptic neurotransmitter release
- MeSH terms
- Zolpidem, Action Potentials, Animals, Interneurons, Kainic Acid, Kinetics, Models, Neurological, Neural Inhibition, Pyridines, Receptors, GABA-A, Synapses, N-Methylaspartate, Rats, Wistar, Presynaptic Terminals, Patch-Clamp Techniques, GABA Agonists, Neocortex, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review