The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Presynaptic regulation of recurrent excitation by D1 receptors in prefrontal circuits
Open accessAbstract
The prefrontal cortex plays a fundamental role in the working memory functions of the cerebral cortex and is also the site of dysfunction in several neurological and psychiatric disorders, including schizophrenia. Prefrontal neurons are distinguished by their capacity for sustained activity during the time a stimulus is held in memory, and this mnemonic response is considered a substrate for a variety of cognitive functions. The neuronal basis for sustained activity in prefrontal neurons is unknown but is thought to involve recurrent excitation among pyramidal neurons. Recent studies in awake behaving monkeys have demonstrated that the persistent activity in prefrontal neurons is modulated by dopamine. To examine the mechanisms by which dopamine might modulate transmission in local excitatory circuits, we have performed dual whole-cell recordings in connected pyramidal cell pairs with and without dopamine application. We find that dopamine reduces the efficacy of unitary excitatory neurotransmission in layer V pyramidal cells by decreasing its reliability. These effects, which are reproduced by a selective D1 agonist and blocked by a D1 antagonist, are independent of voltage changes and are not attenuated by blockade of sodium and potassium channels in the postsynaptic neurons. We conclude that attenuation of local horizontal excitatory synaptic transmission in layer V pyramidal neurons by dopamine is through D1 actions at a presynaptic site.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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
“Dopamine also reduces recurrent excitation in layer V pyramidal neurons 50”
From Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications (2022) · cites this paper as [50]
Citations
Cites
Dopamine receptors: from structure to function
MISSALE, C., NASH, S. R., ROBINSON, S. W., JABER, M., & CARON, M. G. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.1.189 · Cited by 3,633
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Self-citationFuster, J. M. (1997) · Cited by 2,095
Modulation of memory fields by dopamine Dl receptors in prefrontal cortex
Williams, G. V., & Goldman-Rakic, P. S. (1995) · Nature · doi:10.1038/376572a0 · Cited by 1,593
Short-Term Synaptic Plasticity
Zucker, R. S. (1989) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.12.030189.000305 · Cited by 1,450
Compte, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.910 · Cited by 1,143
Markram, H., Lübke, J., Frotscher, M., Roth, A., & Sakmann, B. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp022031 · Cited by 960
Synaptic basis of cortical persistent activity: the importance of NMDA receptors to working memory
Wang, X.-J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09587.1999 · Cited by 859
Stuart, G. J., Dodt, H., & Sakmann, B. J. (1993) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374949 · Cited by 800
Presynaptic inhibition of elicited neurotransmitter release
Wu, L., & Saggau, P. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)01015-6 · Cited by 627
Research works printed but not linked: 2
- C R Yang, J K Seamans, N Gorelova Neuropharmacology 21, 161–194 (1999).
- S Tanaka Prog Neuropsychopharmacol Biol Psychiatry 25, 1–23 (2000).
Cited by
Sorted by citations
Items 101–200 of 254
Developmental alterations in the functional properties of excitatory neocortical synapses
Feldmeyer, D., & Radnikow, G. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.169458 · Cited by 64
Urban, N. N., González‐Burgos, G., Henze, D. A., Lewis, D. A., & Barrionuevo, G. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.015024 · Cited by 60
Bisagno, V., González, B., & Urbano, F. J. (2016) · Pharmacological Research · doi:10.1016/j.phrs.2016.01.013 · Cited by 59
Selemon, L. D., Begović, A., Goldman‐Rakic, P. S., & Castner, S. A. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301179 · Cited by 58
Self-citationLi, Y., Liu, G., Hu, J., Gao, W., & Huang, Y. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06720.x · Cited by 59
Self-citationBidirectional causality between addiction and cognitive deficits
Melugin, P. R., Nolan, S. O., & Siciliano, C. A. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.11.001 · Cited by 59
Amelioration of ketamine-induced working memory deficits by dopamine D1 receptor agonists
Roberts, B. M., Seymour, P. A., Schmidt, C. J., Williams, G. V., & Castner, S. A. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1840-9 · Cited by 56
Wang, M., Datta, D., Enwright, J. F., Galvin, V. C., Yang, S., Paspalas, C. D., Kozak, R., Gray, D. L., Lewis, D. A., & Arnsten, A. F. T. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.03.001 · Cited by 55
Wang, H., Kim, S. S., & Zhuo, M. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.116293 · Cited by 52
D1/D5Modulation of Synaptic NMDA Receptor Currents
Varela, J. A., Hirsch, S. J., Chapman, D. E., Leverich, L. S., & Greene, R. W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4746-08.2009 · Cited by 56
Towers, S. K., & Hestrin, S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5079-07.2008 · Cited by 52
Prenatal cocaine exposure specifically alters spontaneous alternation behavior
Thompson, B. L., Levitt, P. R., & Stanwood, G. D. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.06.010 · Cited by 52
Lörincz, M. L., & Adamantidis, A. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.09.003 · Cited by 54
Local Application of Dopamine Inhibits Pyramidal Tract Neuron Activity in the Rodent Motor Cortex
Awenowicz, P. W., & Porter, L. L. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00078.2002 · Cited by 51
Yang, J., Ye, M., Tian, C., Yang, M., Wang, Y., & Shu, Y. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2013.251058 · Cited by 53
Onn, S., Wang, X.-B., Lin, M., & Grace, A. A. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300829 · Cited by 50
González‐Burgos, G., Kroener, S., Seamans, J. K., Lewis, D. A., & Barrionuevo, G. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00698.2005 · Cited by 51
Schizophrenia endophenotypes as treatment targets
Thaker, G. K. (2007) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.11.9.1189 · Cited by 50
Implications of synaptic biophysics for recurrent network dynamics and active memory
Durstewitz, D. (2009) · Neural Networks · doi:10.1016/j.neunet.2009.07.016 · Cited by 55
Burke, K. J., Keeshen, C. M., & Bender, K. J. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.030 · Cited by 49
Orozco-Cabal, L. F., Liu, J., Pollandt, S., Schmidt, K., Shinnick‐Gallagher, P., & Gallagher, J. P. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2666-07.2008 · Cited by 46
Dopamine controls fundamental cognitive operations of multi-target spatial working memory
Tanaka, S. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00050-3 · Cited by 46
Dopamine Modulation of the Prefrontal Cortex and Cognitive Function
Seamans, J. K., & Robbins, T. W. (2009) · Humana Press eBooks · doi:10.1007/978-1-60327-333-6_14 · Cited by 47
Distribution of neurons expressing tyrosine hydroxylase in the human cerebral cortex
Benavides‐Piccione, R., & DeFelipe, J. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00760.x · Cited by 45
A Model of Prefrontal Cortex Dopaminergic Modulation during the Delayed Alternation Task
Dreher, J., Guigon, E., & Burnod, Y. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/089892902760191081 · Cited by 45
Chadderdon, G. L., & Sporns, O. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/089892906775783624 · Cited by 42
Caruana, D. A., Sorge, R. E., Stewart, J., & Chapman, C. A. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00572.2006 · Cited by 43
Prefrontal dopamine regulates fear reinstatement through the downregulation of extinction circuits
HitoraーImamura, N., Miura, Y., Teshirogi, C., Ikegaya, Y., Matsuki, N., & Nomura, H. (2015) · eLife · doi:10.7554/elife.08274 · Cited by 43
Nakako, T., Murai, T., Ikejiri, M., Ishiyama, T., Taiji, M., & Ikeda, K. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.012 · Cited by 42
Dopamine Modulates Temporal Dynamics of Feedforward Inhibition in Rat Prefrontal Cortex In Vivo
Tierney, P. L., Thierry, A. M., Glowinski, J., Deniau, J., & Gioanni, Y. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm252 · Cited by 44
Dopamine prevents muscarinic-induced decrease of glutamate release in the auditory cortex
Atzori, M., Kanold, P. O., Pineda, J. C., Flores‐Hernández, J., & Paz, R. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.05.005 · Cited by 40
Aghajanian, G. K. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1484-9 · Cited by 42
Korchounov, A., Ilic, T. V., & Ziemann, U. (2006) · Journal of Neural Transmission · doi:10.1007/s00702-006-0523-5 · Cited by 36
Glausier, J. R., Khan, Z. U., & Muly, E. C. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21710 · Cited by 38
Wu, J., Dougherty, J. J., & Nichols, R. A. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03901.x · Cited by 36
Wang, H.-X., & Gao, W. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.024 · Cited by 33
Self-citationNeurocognitive and neurophysiological endophenotypes in schizophrenia: An overview
Donati, F. L., D’Agostino, A., & Ferrarelli, F. (2020) · Biomarkers in Neuropsychiatry · doi:10.1016/j.bionps.2020.100017 · Cited by 33
Lambe, E. K., & Aghajanian, G. K. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.048 · Cited by 37
Vijayraghavan, S., Major, A. J., & Everling, S. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00091 · Cited by 34
Wang, Z., Feng, X., & Zheng, P. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00113-6 · Cited by 32
Ninan, I., & Wang, R. Y. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02549.x · Cited by 32
González, B., Rivero‐Echeto, M. C., Muñiz, J. A., Cadet, J. L., García‐Rill, E., Urbano, F. J., & Bisagno, V. (2015) · Addiction Biology · doi:10.1111/adb.12249 · Cited by 31
Fazio, L., Pergola, G., Papalino, M., Carlo, P. D., Monda, A., Gelao, B., Amoroso, N., Tangaro, S., Rampino, A., Popolizio, T., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717135115 · Cited by 30
Haß, J., Hertäg, L., & Durstewitz, D. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004930 · Cited by 33
Regulation of neuromodulator receptor efficacy?implications for whole-neuron and synaptic plasticity
Scheler, G. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.008 · Cited by 34
Endogenous Dopamine Amplifies Ischemic Long-Term Potentiation via D1 Receptors
Saulle, E., Centonze, D., Martín, A. B. B., Moratalla, R., Bernardi, G., & Calabresi, P. (2002) · Stroke · doi:10.1161/01.str.0000038093.42512.0f · Cited by 31
Circuit-based Localization of Ferret Prefrontal Cortex
Duque, A., & McCormick, D. A. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp164 · Cited by 30
Dopamine Receptor Expression Among Local and Visual Cortex-Projecting Frontal Eye Field Neurons
Mueller, A. L., Krock, R. M., Shepard, S. B., & Moore, T. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz078 · Cited by 33
Synapse-specific contributions in the cortical pathology of schizophrenia
Seshadri, S., Zeledón, M., & Sawa, A. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.01.009 · Cited by 32
Yuen, E. Y., & Yan, Z. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.221416 · Cited by 29
Leon‐Sarmiento, F. E., Rizzo-Sierra, C. V., Bayona, E. A., Bayona-Prieto, J., Doty, R. L., & Bara‐Jimenez, W. (2013) · Archives of Medical Research · doi:10.1016/j.arcmed.2013.03.003 · Cited by 28
Oleson, E. B., Hamilton, L. R., & Gomez, D. M. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.660218 · Cited by 28
Young, C. E., & Yang, C. R. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04161.x · Cited by 27
Dopaminergic Suppression of Synaptic Transmission in the Lateral Entorhinal Cortex
Caruana, D. A., & Chapman, C. A. (2008) · Neural Plasticity · doi:10.1155/2008/203514 · Cited by 26
Amphetamine depresses excitatory synaptic transmission at prefrontal cortical layer V synapses
Mair, R. D., & Kauer, J. A. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.004 · Cited by 26
Hoeppner, J., Wandschneider, R., Neumeyer, M., Gierow, W., Haessler, F., Herpertz, S. C., & Buchmann, J. A. (2008) · Journal of Neural Transmission · doi:10.1007/s00702-007-0008-1 · Cited by 26
David, H., & Abraini, J. H. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00052-2 · Cited by 26
Mayne, E. W., Craig, M. T., McBain, C. J., & Paulsen, O. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12125 · Cited by 26
A model of dopamine modulated cortical activation
Ashby, F. G., & Casale, M. B. (2003) · Neural Networks · doi:10.1016/s0893-6080(03)00051-0 · Cited by 25
Glovaci, I., Caruana, D. A., & Chapman, C. A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.076 · Cited by 24
Comodulation of dopamine and serotonin on prefrontal cortical rhythms: a theoretical study
Wang, D., & Wong‐Lin, K. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00054 · Cited by 24
Gao, W. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00400.2006 · Cited by 24
Self-citationDziedzicka‐Wasylewska, M., Faron‐Górecka, A., Górecki, A., & Kuśemider, M. (2008) · PubMed · Cited by 23
5.3 Dopamine’s Influence on Prefrontal Cortical Cognition: Actions and Circuits in Behaving Primates
Arnsten, A. F. T., Vijayraghavan, S., Wang, M., Gamo, N. J., & Paspalas, C. D. (2009) · Dopamine Handbook · doi:10.1093/acprof:oso/9780195373035.003.0016 · Cited by 23
Okimura, T., Tanaka, S., Maeda, T., Kato, M., & Mimura, M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.03.039 · Cited by 21
Dopaminergic neuromodulation of semantic priming in a cortical network model
Lavigne, F., & Darmon, N. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.06.019 · Cited by 21
Multi-directional representation of spatial working memory in a model prefrontal cortical circuit
Tanaka, S. (2002) · Neurocomputing · doi:10.1016/s0925-2312(02)00503-9 · Cited by 21
Schaffner, K. F. (2001) · Current Opinion in Psychiatry · doi:10.1097/00001504-200109000-00011 · Cited by 22
Sleep and Plasticity in Schizophrenia
Sprecher, K. E., Ferrarelli, F., & Benca, R. M. (2015) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_366 · Cited by 20
Tse, M., Cantor, A., & Floresco, S. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1810-11.2011 · Cited by 20
Regulation of complexin 1 and complexin 2 in the developing human prefrontal cortex
Salimi, K., Glantz, L. A., Hamer, R. M., German, T. T., Gilmore, J. H., & Jarskog, L. F. (2008) · Synapse · doi:10.1002/syn.20492 · Cited by 20
Dopamine Gates Visual Signals in Monkey Prefrontal Cortex Neurons
Stalter, M., Westendorff, S., & Nieder, A. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.11.082 · Cited by 21
Schizophrenia, the prefrontal cortex, and a mechanism of genetic susceptibility
Weinberger, D. (2002) · European psychiatry · doi:10.1016/s0924-9338(03)00080-4 · Cited by 22
Catecholaminergic Innervation of Pyramidal Neurons in the Human Temporal Cortex
Benavides‐Piccione, R., Arellano, J. I., & DeFelipe, J. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi036 · Cited by 19
Banks, P. J., Warburton, E. C., & Bashir, Z. I. (2021) · Cerebral Cortex Communications · doi:10.1093/texcom/tgab029 · Cited by 21
Qi, G., Yang, D., Ding, C., & Feldmeyer, D. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00005 · Cited by 16
The Unique Properties of the Prefrontal Cortex and Mental Illness
Gao, W., Wang, H.-X., Melissa, A., & Li, Y. (2012) · InTech eBooks · doi:10.5772/35868 · Cited by 17
Self-citationWang, H., Waterhouse, B. D., & Gao, W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.009 · Cited by 17
Self-citationKatsuki, F., & Constantinidis, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081601 · Cited by 17
van Onselen, R., & Downing, T. G. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00434-x · Cited by 17
Agster, K. L., Clark, B., Gao, W., Shumsky, J. S., Wang, H. X., Berridge, C. W., & Waterhouse, B. D. (2011) · The Anatomical Record · doi:10.1002/ar.21403 · Cited by 16
Self-citationCoppa-Hopman, R., Galle, J., & Pimkine, D. (2008) · Journal of Psychopharmacology · doi:10.1177/0269881108091256 · Cited by 15
Section II. The Dopamine System
Smythies, J. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)64002-0 · Cited by 15
Tzavellas, N. P., Tsamis, K. I., Katsenos, A. P., Davri, A. S., Simos, Y. V., Nikas, I. P., Bellos, S., Lekkas, P., Kanellos, F. S., Konitsiotis, S., et al. (2024) · Cells · doi:10.3390/cells13050434 · Cited by 16
Lower neuronal variability in the monkey dorsolateral prefrontal than posterior parietal cortex
Qi, X.-L., & Constantinidis, C. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00454.2015 · Cited by 14
Pharmacogenetic tools for the development of target-oriented cognitive-enhancing drugs
Apud, J. A., & Weinberger, D. R. (2006) · NeuroRx · doi:10.1016/j.nurx.2005.12.004 · Cited by 14
Early hypersynchrony in juvenile PINK1−/− motor cortex is rescued by antidromic stimulation
Carron, R., Filipchuk, A., Nardou, R., Singh, A. K., Michel, F. J., Humphries, M. D., & Hammond, C. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00095 · Cited by 13
Dopamine‐Acetylcholine Interactions in the Modulation of Glutamate Release
Atzori, M., Kanold, P. O., Pineda, J. C., & Flores‐Hernández, J. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.022 · Cited by 12
Circuit simulation of memory field modulation by dopamine Dl receptor activation
Yamashita, K., & Tanaka, S. (2002) · Neurocomputing · doi:10.1016/s0925-2312(02)00508-8 · Cited by 12
Multi-Scale Expressions of One Optimal State Regulated by Dopamine in the Prefrontal Cortex
Hu, G., Huang, X., Jiang, T., & Yu, S. P. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00113 · Cited by 11
Dopaminergic Modulation of Prefrontal Cortex Network Dynamics
Durstewitz, D. (2007) · Springer eBooks · doi:10.1007/978-0-387-72256-6_15 · Cited by 11
Hypertension-induced changes in monoamine receptors in the prefrontal cortex of rhesus monkeys
Moore, T. L., Killiany, R., Rosene, D. L., Prusty, S., Hollander, W., & Moss, M. B. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00242-2 · Cited by 10
Bulumulla, C., Zhang, D., Walpita, D., Iyer, N., Eddison, M., Ackerman, D., Otsuna, H., Zhao, X., Zhang, S., Gao, S. M., et al. (2026) · Science Advances · doi:10.1126/sciadv.aei0203 · Cited by 8
Hutter, J. A., Martel, A., Trigiani, L. J., Barrett, S. G., & Chapman, C. A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.05.057 · Cited by 8
Buchmann, J. A., Dück, A., Gierow, W., Zamorski, H., Heinicke, S., Heinrich, H., Hoeppner, J., Klauer, T., Reis, O., & Haessler, F. (2009) · Journal of Neural Transmission · doi:10.1007/s00702-009-0349-z · Cited by 8
Yin, Y., Hu, J., Wu, H., Yang, X., Qi, J., Huang, L., Luo, Z.-Y., Jin, S., Hu, N.-Y., Luo, Z.-C., et al. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.07.034 · Cited by 7
Adolescent Maturation of Cortical Dopamine
O’Donnell, P. (2010) · Springer eBooks · doi:10.1007/978-1-4614-0785-0_11 · Cited by 7
González‐Burgos, G., Miyamae, T., Reddy, N., Dawkins, S., Chen, C., Hill, A., Enwright, J. F., Ermentrout, B., & Lewis, D. A. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad077 · Cited by 9
Li, S., Rosen, M. C., Chang, S., David, S., & Freedman, D. J. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1213435 · Cited by 10
Local Circuit Neurons in the Frontal Cortico-Striatal System
Kawaguchi, Y. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0039-1_9 · Cited by 7
Metadata
- Authors
- Gao, W.-J., Krimer, L. S., & Goldman-Rakic, P. S.
- Affiliations
- Yale University (US)
- Section of Neurobiology, Yale University School of Medicine, 333 Cedar Street, New Haven, CT 06510
- ORCID
- Gao, Wen-Jun
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2000-12-26
- Volume
- 98
- Issue
- 1
- Pages
- 295-300
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC14584
- OpenAlex
- W2154397718
- Cited by
- 257
- References
- 37
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 8 · 2023: 2 · 2022: 2 · 2021: 4 · 2020: 9 · 2019: 6 · 2018: 6 · 2017: 5 · 2016: 4 · 2015: 11 · 2014: 10 · 2013: 15 · 2012: 7
- FWCI
- 5.29
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (R01MH038546, P50 MH44866, R01 MH38546, R37MH038546, P50MH044866, R01MH085666)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- dopamine D1 receptor, presynaptic modulation, recurrent excitation, prefrontal cortex, layer 5 pyramidal neurons, persistent neuronal activity, working memory, synaptic reliability, schizophrenia
- MeSH terms
- Animals, Benzazepines, Dopamine, Ferrets, Synaptic Transmission, Schizophrenia, Wakefulness, Potassium Channels, Sodium Channels, Prefrontal Cortex, Receptors, Dopamine D1, Presynaptic Terminals, Pyramidal Cells, Patch-Clamp Techniques, Dopamine Agonists, Dopamine Antagonists, Excitatory Postsynaptic Potentials, Raclopride, In Vitro Techniques
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