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Destruction and Creation of Spatial Tuning by Disinhibition: GABAABlockade of Prefrontal Cortical Neurons Engaged by Working Memory
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Local circuit neurons in the dorsolateral prefrontal cortex (dPFC) of monkeys have been implicated in the cellular basis of working memory. To further elucidate the role of inhibition in spatial tuning, we iontophoresed bicuculline methiodide (BMI) onto functionally characterized neurons in the dPFC of monkeys performing an oculomotor delayed response task. This GABA A blockade revealed that both putative interneurons and pyramidal cells possess significant inhibitory tone in the awake, behaving monkey. In addition, BMI application primarily resulted in the loss of previously extant spatial tuning in both cell types through reduction of both isodirectional and cross-directional inhibition. This tuning loss occurred in both the sensorimotor and mnemonic phases of the task, although the delay activity of prefrontal neurons appeared to be particularly affected. Finally, application of BMI also created significant spatial tuning in a sizable minority of units that were untuned in the control condition. Visual field analysis of such tuning suggests that it is likely caused by the unmasking of normally suppressed spatially tuned excitatory input. These findings provide the first direct evidence of directional inhibitory modulation of pyramidal cell and interneuron firing in both the mnemonic and sensorimotor phases of the working memory process, and they implicate a further role for GABAergic interneurons in the construction of spatial tuning in prefrontal cortex.
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“Primate electrophysiological studies show that persistent firing of prefrontal pyramidal cells supports robust and stable WM representations (Funahashi et al. 1989) that depend critically on E/I balance (Rao et al. 2000).”
From Linking microcircuit dysfunction to cognitive impairment: Effects of disinhibition associated with schizophrenia in a cortical working memory model (2014) · cites this paper as Rao et al. 2000
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Cites
Baddeley, A. (1992) · Science · doi:10.1126/science.1736359 · Cited by 5,258
Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex
Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Self-citationStatistical Analysis of Circular Data.
LANGE, N. D., & Fisher, N. I. (1995) · Journal of the American Statistical Association · doi:10.2307/2291098 · Cited by 2,155
Statistical Analysis of Circular Data
Fisher, N. I. (1993) · Cambridge University Press eBooks · doi:10.1017/cbo9780511564345 · Cited by 1,826
GABAergic cell subtypes and their synaptic connections in rat frontal cortex
Kawaguchi, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.476 · Cited by 1,416
Reshaping the Cortical Motor Map by Unmasking Latent Intracortical Connections
Jacobs, K. M., & Donoghue, J. P. (1991) · Science · doi:10.1126/science.2000496 · Cited by 1,004
Recurrent Excitation in Neocortical Circuits
Douglas, R. J., Christof Koch, A., Mahowald, M. A., Martin, K. A. C., & Suarez, H. H. (1995) · Science · doi:10.1126/science.7638624 · Cited by 985
Chafee, M. V., & Goldman, P. S. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.6.2919 · Cited by 666
Architecture of the Prefrontal Cortex and the Central Executive
Goldman, P. S. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb38132.x · Cited by 654
Research works printed but not linked: 1
- Williams, 1997, Attenuation of memory fields in primate prefrontal cortical pyramidal cells and interneurons by selective 5-HT2 antagonists., Soc Neurosci Abstr, 23, 627.7
Cited by
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Cortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297
The principal features and mechanisms of dopamine modulation in the prefrontal cortex
Seamans, J. K., & Yang, C. R. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.05.006 · Cited by 1,592
Neural syntax: cell assemblies, synapsembles, and readers
Buzsáki, G. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.023 · Cited by 1,289
Compte, A. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.910 · Cited by 1,143
Interneuron dysfunction in psychiatric disorders
Marín, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3155 · Cited by 1,190
GABAergic Interneurons Implications for Understanding Schizophrenia and Bipolar Disorder
Benes, F. (2001) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00225-1 · Cited by 1,082
Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory
Vijayraghavan, S., Wang, M., Birnbaum, S. G., Williams, G. V., & Arnsten, A. F. T. (2007) · Nature Neuroscience · doi:10.1038/nn1846 · Cited by 1,013
Self-citationThe role of default network deactivation in cognition and disease
Anticevic, A., Cole, M. W., Murray, J. D., Corlett, P. R., Wang, X.-J., & Krystal, J. H. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.008 · Cited by 978
The Neuropsychopharmacology of Fronto-Executive Function: Monoaminergic Modulation
Robbins, T. W., & Arnsten, A. F. T. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135535 · Cited by 957
Hashimoto, T., Volk, D. W., Eggan, S. M., Mirnics, K., Pierri, J. N., Sun, Z., Sampson, A. R., & Lewis, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06315.2003 · Cited by 938
Neurocomputational models of working memory
Durstewitz, D., Seamans, J. K., & B, T. J. S. A. (2000) · Nature Neuroscience · doi:10.1038/81460 · Cited by 729
Origins of Cortical Interneuron Subtypes
Xu, Q., Cobos, I., De La Cruz, E., Rubenstein, J. L., & Anderson, S. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5667-03.2004 · Cited by 639
Ferguson, B. R., & Gao, W.-J. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00037 · Cited by 594
Adrenergic pharmacology and cognition: Focus on the prefrontal cortex
Ramos, B. P., & Arnsten, A. F. T. (2007) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.11.006 · Cited by 641
Ketamine-Induced Loss of Phenotype of Fast-Spiking Interneurons Is Mediated by NADPH-Oxidase
Behrens, M. M., Ali, S. S., Dao, D. N., Lucero, J., Shekhtman, G., Quick, K. L., & Dugan, L. L. (2007) · Science · doi:10.1126/science.1148045 · Cited by 585
Dopamine and Cognitive Control in Prefrontal Cortex
Ott, T., & Nieder, A. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.12.006 · Cited by 530
Gao, R., & Penzes, P. (2015) · Current Molecular Medicine · doi:10.2174/1566524015666150303003028 · Cited by 516
“For example, PV+ neurons in the monkey DLPFC are active during the delay period of working memory tasks [59], and are responsible for spatial tuning of neuronal responses during this period [60].”
BackgroundKrystal, J. H., D'Souza, D. C., Mathalon, D., Perry, E., Belger, A., & Hoffman, R. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1582-z · Cited by 530
Wang, M., Yang, Y., Wang, C.-J., Gamo, N. J., Jin, L. E., Mazer, J. A., Morrison, J. H., Wang, X.-J., & Arnsten, A. F. T. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.032 · Cited by 489
Hashimoto, T., Arion, D., Unger, T., Maldonado-Avilés, J. G., Morris, H. M., Volk, D. W., Mirnics, K., & Lewis, D. A. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002011 · Cited by 490
Hashimoto, T., Bazmi, H. H., Mirnics, K., Wu, Q., Sampson, A. R., & Lewis, D. A. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2007.07081223 · Cited by 457
Adolescent Brain Development and the Risk for Alcohol and Other Drug Problems
Bava, S., & Tapert, S. F. (2010) · Neuropsychology Review · doi:10.1007/s11065-010-9146-6 · Cited by 484
Rajkowska, G., O'Dwyer, G., Teleki, Z., Stockmeier, C. A., & Miguel-Hidalgo, J. J. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301234 · Cited by 430
Bidirectional dopamine modulation of GABAergic inhibition in prefrontal cortical pyramidal neurons
Seamans, J. K., Gorelova, N., Durstewitz, D., & Yang, C. R. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03628.2001 · Cited by 507
Cognitive Dysfunction in Schizophrenia: Convergence of γ-Aminobutyric Acid and Glutamate Alterations
Lewis, D. A., & Moghaddam, B. (2006) · Archives of Neurology · doi:10.1001/archneur.63.10.1372 · Cited by 404
Tseng, K. Y., & O'Donnell, P. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1021-04.2004 · Cited by 402
Nieder, A. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.40 · Cited by 406
Hashimoto, T., Bergen, S. E., Nguyen, Q. L., Xu, B., Monteggia, L. M., Pierri, J. N., Sun, Z., Sampson, A. R., & Lewis, D. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4035-04.2005 · Cited by 386
Prefrontal Cortical Dendritic Spine Pathology in Schizophrenia and Bipolar Disorder
Konopaske, G. T., LANGE, N. D., Coyle, J. T., & Benes, F. M. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.1582 · Cited by 379
Mechanism for top-down control of working memory capacity
Edin, F., Klingberg, T., Johansson, P., McNab, F., Tegnér, J., & Compte, A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901894106 · Cited by 365
Neuroplasticity of Neocortical Circuits in Schizophrenia
Lewis, D. A., & González‐Burgos, G. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301563 · Cited by 372
Bissonette, G. B., Martins, G. J., Franz, T. M., Harper, E. S., Schoenbaum, G., & Powell, E. M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2820-08.2008 · Cited by 353
Bossong, M. G., & Niesink, R. J. M. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.06.010 · Cited by 333
Hyde, T. M., Lipska, B. K., Ali, T., Mathew, S., Law, A. J., Metitiri, O. E., Straub, R. E., Ye, T., Colantuoni, C., Herman, M. M., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1234-11.2011 · Cited by 325
Pathophysiologically based treatment interventions in schizophrenia
Lewis, D. A., & González‐Burgos, G. (2006) · Nature Medicine · doi:10.1038/nm1478 · Cited by 324
Constantinidis, C., & Goldman, P. S. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00188.2002 · Cited by 330
George, O., & Koob, G. F. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.05.002 · Cited by 322
Foss‐Feig, J. H., Adkinson, B. D., Ji, J. L., Yang, G., Srihari, V. H., McPartland, J. C., Krystal, J. H., Murray, J. D., & Anticevic, A. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.03.005 · Cited by 328
The Physiological Role of 5-HT2AReceptors in Working Memory
Williams, G. V., Rao, S. G., & Goldman-Rakic, P. S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02843.2002 · Cited by 311
Self-citationGorelova, N., Seamans, J. K., & Yang, C. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00335.2002 · Cited by 302
A role for inhibition in shaping the temporal flow of information in prefrontal cortex
Constantinidis, C., Williams, G. V., & Goldman-Rakic, P. S. (2002) · Nature Neuroscience · doi:10.1038/nn799 · Cited by 348
Self-citationLewis, D. A., Cho, R. Y., Carter, C. S., Eklund, K. E., Förster, S., Kelly, M. A., & Montrose, D. M. (2008) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.08030395 · Cited by 291
Trantham‐Davidson, H., Neely, L. C., Lavı́n, A., & Seamans, J. K. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3179-04.2004 · Cited by 284
Eggan, S. M., & Lewis, D. A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj136 · Cited by 272
Murray, J. D., Anticevic, A., Gancsos, M., Ichinose, M., Corlett, P. R., Krystal, J. H., & Wang, X.-J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs370 · Cited by 255
GABAergic dysfunction in schizophrenia: new treatment strategies on the horizon
Guidotti, A., Auta, J., Davis, J. M., Dong, E., Grayson, D. R., Veldic, M., Zhang, X., & Costa, E. (2005) · Psychopharmacology · doi:10.1007/s00213-005-2212-8 · Cited by 262
Under the curve: Critical issues for elucidating D1 receptor function in working memory
Williams, G. V., & Castner, S. A. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.09.028 · Cited by 326
Self-citationThe role of synaptic ion channels in synaptic plasticity
Voglis, G., & Tavernarakis, N. (2006) · EMBO Reports · doi:10.1038/sj.embor.7400830 · Cited by 267
Lewis, D., Volk, D., & Hashimoto, T. (2004) · Psychopharmacology · doi:10.1007/s00213-003-1673-x · Cited by 253
Role of Prefrontal Persistent Activity in Working Memory
Riley, M. R., & Constantinidis, C. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00181 · Cited by 251
Delevich, K., Tucciarone, J., Huang, Z. J., & Li, B. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4565-14.2015 · Cited by 226
GABA and Schizophrenia: A Review of Basic Science and Clinical Studies
Wassef, A. A., Baker, J. D., & Kochan, L. D. (2003) · Journal of Clinical Psychopharmacology · doi:10.1097/01.jcp.0000095349.32154.a5 · Cited by 248
Rujescu, D., Bender, A., Keck, M. E., Hartmann, A. M., Ohl, F., Ræder, H., Giegling, I., Genius, J., McCarley, R. W., Möller, H., et al. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.08.029 · Cited by 241
Can noninvasive brain stimulation enhance cognition in neuropsychiatric disorders?
Demirtas-Tatlidede, A., Vahabzadeh-Hagh, A. M., & Pascual-Leone, A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.020 · Cited by 236
Watanabe, K., & Funahashi, S. (2014) · Nature Neuroscience · doi:10.1038/nn.3667 · Cited by 222
Lewis, D. A., & Sweet, R. A. (2009) · Journal of Clinical Investigation · doi:10.1172/jci37335 · Cited by 242
Gamo, N. J., Wang, M., & Arnsten, A. F. T. (2010) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2010.06.015 · Cited by 232
Amyloid beta peptides and glutamatergic synaptic dysregulation
Parameshwaran, K., Dhanasekaran, M., & Suppiramaniam, V. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.10.008 · Cited by 235
Smucny, J., Dienel, S. J., Lewis, D. A., & Carter, C. S. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01089-0 · Cited by 231
Molecular Targets for Treating Cognitive Dysfunction in Schizophrenia
Gray, J. A., & Roth, B. L. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm074 · Cited by 227
Distinct Roles of Parvalbumin- and Somatostatin-Expressing Interneurons in Working Memory
Kim, D., Jeong, H., Lee, J., Ghim, J.-W., Her, E. S., Lee, S.-H., & Jung, M. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.023 · Cited by 201
Behavioral planning in the prefrontal cortex
Tanji, J., & Hoshi, E. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00192-6 · Cited by 224
The Role of the Endocannabinoid System and Genetic Variation in Adolescent Brain Development
Meyer, H. C., Lee, F. S., & Gee, D. G. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.143 · Cited by 238
Reduced Cortical Cannabinoid 1 Receptor Messenger RNA and Protein Expression in Schizophrenia
Eggan, S. M., Hashimoto, T., & Lewis, D. A. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.7.772 · Cited by 224
A Neural Circuit Basis for Spatial Working Memory
Constantinidis, C., & Wang, X. (2004) · The Neuroscientist · doi:10.1177/1073858404268742 · Cited by 223
Animal models of working memory: insights for targeting cognitive dysfunction in schizophrenia
Castner, S. A., Goldman‐Rakic, P. S., & Williams, G. (2004) · Psychopharmacology · doi:10.1007/s00213-003-1710-9 · Cited by 211
Self-citationAbdul-Monim, Z., Neill, J. C., & Reynolds, G. P. (2007) · Journal of Psychopharmacology · doi:10.1177/0269881107067097 · Cited by 206
Ferguson, B. R., & Gao, W.-J. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.033 · Cited by 186
γ-Aminobutyric Acid Type A Receptors and Alcoholism
Krystal, J. H., Staley, J. K., Mason, G. F., Petrakis, I. L., Kaufman, J., Harris, R. A., Gelernter, J. E., & Lappalainen, J. (2006) · Archives of General Psychiatry · doi:10.1001/archpsyc.63.9.957 · Cited by 195
Tian, Y., Baek, J., Lee, S., & Jang, C. (2010) · Synapse · doi:10.1002/syn.20746 · Cited by 197
Caballero, A., Flores-Barrera, E., Cass, D. K., & Tseng, K. Y. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0508-8 · Cited by 178
Krystal, J. H., Anticevic, A., Yang, G., Dragoi, G., Driesen, N. R., Wang, X., & Murray, J. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.01.004 · Cited by 201
Influence of the hippocampus on interneurons of the rat prefrontal cortex
Tierney, P. L., Dégenètais, E., Thierry, A., Glowinski, J., & Gioanni, Y. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03501.x · Cited by 192
Development of the GABAergic System from Birth to Adolescence
Kilb, W. (2012) · The Neuroscientist · doi:10.1177/1073858411422114 · Cited by 190
Late Development of the GABAergic System in the Human Cerebral Cortex and White Matter
Xu, G., Broadbelt, K. G., Haynes, R. L., Folkerth, R. D., Borenstein, N. S., Belliveau, R. A., Trachtenberg, F. L., Volpe, J. J., & Kinney, H. C. (2011) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e31822f471c · Cited by 188
Jiménez-Baladó, J., & Eich, T. S. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.01.005 · Cited by 194
Enomoto, T., Tse, M. T., & Floresco, S. B. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.038 · Cited by 179
Zaitsev, A. V., González‐Burgos, G., Povysheva, N. V., Kröner, S., Lewis, D. A., & Krimer, L. S. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh218 · Cited by 184
Signaling pathways in schizophrenia: emerging targets and therapeutic strategies
Karam, C. S., Ballon, J. S., Bivens, N. M., Freyberg, Z., Girgis, R. R., Lizardi-Ortiz, J. E., Markx, S., Lieberman, J. A., & Javitch, J. A. (2010) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2010.05.004 · Cited by 180
Prefrontal cortical network connections: key site of vulnerability in stress and schizophrenia
Arnsten, A. F. T. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.02.006 · Cited by 182
Buchanan, R. W., Keefe, R. S. E., Lieberman, J. A., Barch, D. M., Csernansky, J. G., Goff, D. C., Gold, J. M., Green, M. F., Jarskog, L. F., Javitt, D. C., et al. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.052 · Cited by 172
Neurofibromin regulates corticostriatal inhibitory networks during working memory performance
Shilyansky, C., Karlsgodt, K. H., Cummings, D. M., Sidiropoulou, K., Hardt, M. E., James, A. S., Ehninger, D., Bearden, C. E., Poirazi, P., Jentsch, J. D., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004829107 · Cited by 170
An astroglia-linked dopamine D2-receptor action in prefrontal cortex
Khan, Z. U., Koulen, P., Rubinstein, M., Grandy, D. K., & Goldman‐Rakic, P. S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.4.1964 · Cited by 169
Self-citationPowell, S. B., Sejnowski, T. J., & Behrens, M. M. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.049 · Cited by 164
Arnsten, A. F. T. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm033 · Cited by 200
Behrens, M. M., & B, T. J. S. A. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.06.002 · Cited by 163
González‐Burgos, G., Krimer, L. S., Povysheva, N. V., Barrionuevo, G., & Lewis, D. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00787.2004 · Cited by 159
Impaired prefrontal inhibition in schizophrenia: relevance for cognitive dysfunction
Volk, D. W., & Lewis, D. A. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00936-8 · Cited by 154
Hashimoto, T., Nguyen, Q. L., Rotaru, D., Keenan, T., Arion, D., Beneyto, M., Gonzalez-Burgos, G., & Lewis, D. A. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.01.004 · Cited by 151
Driesen, N. R., McCarthy, G., Bhagwagar, Z., Bloch, M. H., Calhoun, V. D., D'Souza, D. C., Gueorguieva, R., He, G., Leung, H.-C., Ramani, R., et al. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.170 · Cited by 148
Medalla, M., & Barbas, H. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.006 · Cited by 146
Povysheva, N. V., González‐Burgos, G., Zaitsev, A. V., Kröner, S., Barrionuevo, G., Lewis, D. A., & Krimer, L. S. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj002 · Cited by 145
Krimer, L. S., & Goldman-Rakic, P. S. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-11-03788.2001 · Cited by 141
Neurophysiology and neuroanatomy of reflexive and voluntary saccades in non-human primates
Johnston, K., & Everling, S. (2008) · Brain and Cognition · doi:10.1016/j.bandc.2008.08.017 · Cited by 152
Dopamine Modulation of Perisomatic and Peridendritic Inhibition in Prefrontal Cortex
Gao, W.-J., Wang, Y., & Goldman-Rakic, P. S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01622.2003 · Cited by 134
Tuning the engine of cognition: A focus on NMDA/D1 receptor interactions in prefrontal cortex
Castner, S. A., & Williams, G. V. (2007) · Brain and Cognition · doi:10.1016/j.bandc.2006.11.002 · Cited by 134
Self-citationBoy, F., Evans, J., Edden, R. A. E., Lawrence, A. D., Singh, K. D., Husain, M., & Sumner, P. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.05.030 · Cited by 141
Activity of different classes of neurons of the motor cortex during locomotion
Beloozerova, I. N., Sirota, M. G., & Swadlow, H. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-03-01087.2003 · Cited by 126
Barr, M. S., Farzan, F., Rusjan, P., Chen, R. E., Fitzgerald, P. B., & Daskalakis, Z. J. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.79 · Cited by 128
The Neurodevelopmental Hypothesis of Schizophrenia
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Metadata
- Authors
- Rao, S. G., Williams, G. V., & Goldman-Rakic, P. S.
- Affiliations
- Yale University (US)
- ORCID
- Williams, Graham V.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2000-01-01
- Volume
- 20
- Issue
- 1
- Pages
- 485-494
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6774140
- OpenAlex
- W2170328434
- Cited by
- 407
- References
- 46
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 29 · 2023: 6 · 2022: 9 · 2021: 14 · 2020: 6 · 2019: 10 · 2018: 11 · 2017: 19 · 2016: 12 · 2015: 18 · 2014: 23 · 2013: 15 · 2012: 20
- FWCI
- 7.51
- 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
- National Institute of Mental Health (P50 MH44866, R37 MH-3854, P50MH044866)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- spatial tuning, GABAergic inhibition, disinhibition, dorsolateral prefrontal cortex, working memory, bicuculline methiodide, interneurons, pyramidal neurons, delay activity, visual field testing
- MeSH terms
- Action Potentials, Animals, Bicuculline, Fixation, Ocular, Inhibition, Psychological, Interneurons, Macaca mulatta, Memory, Reaction Time, Receptors, GABA-A, Space Perception, Prefrontal Cortex, GABA Antagonists, GABA-A Receptor Antagonists
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