The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Modulation of memory fields by dopamine Dl receptors in prefrontal cortex
Abstract
Dopamine has been implicated in the cognitive process of working memory but the cellular basis of its action has yet to be revealed. By combining iontophoretic analysis of dopamine receptors with single-cell recording during behaviour, we found that D1 antagonists can selectively potentiate the 'memory fields' of prefrontal neurons which subserve working memory. The precision shown for D1 receptor modulation of mnemonic processing indicates a direct gating of selective excitatory synaptic inputs to prefrontal neurons during cognition.
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“evidence from non‐human primates (Sawaguchi & Goldman‐Rakic, 1991, 1994; Williams & Goldmanrakic, 1995) and in healthy humans (Fischer et al., 2010) showed that dopamine depletion or antagonism impairs visuospatial WM.”
From Systematic reviews of the acute effects of amphetamine on working memory and other cognitive performances in healthy individuals, with a focus on the potential influence of personality traits (2023) · cites this paper as Williams & Goldmanrakic, 1995
In the citing paper
“Third, dopamine exerts a significant influence over prefrontal cortical functions such as working memory (Williams and Goldman-Rakic, 1995), in a manner that depends on initial levels or efficacy of this neuromodulator (Cools and D’Esposito, 2011).”
From Goals and Habits in the Brain (2013) · cites this paper as Williams and Goldman-Rakic, 1995
In the citing paper
“Dopaminergic signalling has a role in the top-down regulation of spatial attention, and D1 dopaminergic receptors modulate response amplitude and selectivity in the dorsolateral prefrontal cortex for preferred spatial locations during working memory tasks204,205.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [205]
In the citing paper
“Dopaminergic signalling has a role in the top-down regulation of spatial attention, and D1 dopaminergic receptors modulate response amplitude and selectivity in the dorsolateral prefrontal cortex for preferred spatial locations during working memory tasks204,205.”
From Mechanisms underlying gain modulation in the cortex (2020) · cites this paper as [205]
In the citing paper
“It is also consistent with a growing literature documenting baseline performance-dependent effects of stimulants and related drugs, which have been explained by a hypothesized inverted U-shaped function, whereby optimal catecholamine levels determine optimal performance, and levels along the curve at either side of the optimum are associated with impaired performance (Robbins and Sahakian, 1979; N”
From A positron emission tomography study of nigro-striatal dopaminergic mechanisms underlying attention: implications for ADHD and its treatment (2013) · cites this paper as Williams and Goldman-Rakic, 1995
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“22 that this deficit is similarly related to disrupted dopamine transmission in PD (Floresco and Phillips 2001; Sawaguchi and Goldman-Rakic 1994; Williams and Goldman-Rakic 1995; Zahrt et al. 1997).”
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“An increase of pyramidal neuron activity in mPFC may balance monoamine neurotransmission in this area and facilitate the activity of mPFC in tasks, such as working memory, which require persistent activity of pyramidal neurons (Williams and Goldman-Rakic 1995; Fuster 2008; Robbins and Arnsten 2009).”
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“…the spatial tuning of working memory fields in behaving primates is abolished by a GABAergic antagonist and enhanced by low doses of a D1 receptor antagonist presumably by removing the D1-mediated modulation of interneuron activity (Williams and Goldman-Rakic 1995; Goldman-Rakic et al. 2000).”
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“However, it is simply unknown whether the D1like receptors play a role in reversal learning, although the D1-like receptors are critically involved in other cognitive functions, such as working memory (Sawaguchi and Goldman-Rakic, 1991; Williams and Goldman-Rakic, 1995) and visual attention (Granon et al, 2000).”
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“DA modulates cognitive processes in the PFC by gating glutamate activity at NMDA receptors (Williams and Goldman-Rakic, 1995).”
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“Among the D2-like family of DRs, the D4 DR (D4R) has been of particular interest because it is densely expressed in the frontal cortex (Mrzljak et al. 1996), a brain region where dopamine signalling may modulate working memory and the establishment of memory fields (Williams & Goldman-Rakic 1995).”
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“These results build on neural recordings in which dopaminergic tuning mechanisms were observed to play key roles in encoding and actively maintaining information signal, and in protecting or stabilizing them against neural noise (Williams and Goldman-Rakic, 1995; Seamans and Yang, 2004; Vijayraghavan et al., 2007).”
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From arousal to cognition: the integrative position of the prefrontal cortex
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“Conversely, dopaminergic dysfunction significantly alters spatial learning and short- and longterm memory in rodents and in nonhuman primates (Whishaw and Dunnett, 1985; Williams and Goldman-Rakic, 1995).”
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“…that examined the effects of various dosages of dopaminergic agonist and antagonist treatments (Arnsten & Goldman-Rakic, 1998; Sawaguchi & GoldmanRakic, 1994; Williams & Goldman-Rakic, 1995; Zahrt et al., 1997), each individual has an optimal dopamine concentration for optimal cognitive processing.”
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“This suggests that the COMT Val allele might increase risk for schizophrenia by enhancing dopamine catabolism, which in turn impairs the functional efficacy of the PFC (Egan et al., 2001, Chen et al., 2004).”
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An in vivo assay of synaptic function mediating human cognition
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Schweitzer, J. B., Lee, D. O., Hanford, R. B., Zink, C. F., Ely, T. D., Tagamets, M. A., Hoffman, J. M., Grafton, S. T., & Kilts, C. D. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.07.011 · Cited by 135
“…i e b i f n F o d c w t t u i a a t s T b t h w cting through D1 receptors, appears to inhibit local excitatory onnections among layer V pyramidal cells in the PFC (Gao et al 001; Williams and Goldman-Rakic 1995) during WM tasks. hese actions likely account for the rCBF reductions we have bserved.”
BackgroundOn the Origin of Cortical Dopamine: Is it a Co-Transmitter in Noradrenergic Neurons?
Devoto, P., & Flore, G. (2006) · Current Neuropharmacology · doi:10.2174/157015906776359559 · Cited by 137
“These catecholamines exert a biphasic effect on cognitive functioning, determining an inverted-U shaped dose-curve, normal cognitive operation occurring only within a limited range of dopaminergic and noradrenergic activity [7, 8, 47, 73, 82, 125].”
BackgroundYoshitake, T., Yoshitake, S., & Kehr, J. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00580.x · Cited by 139
Parsing cognition in schizophrenia using saccadic eye movements: a selective overview
Broerse, A., Crawford, T. J., & den Boer, J. A. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00155-x · Cited by 136
de Frias, C. M., Annerbrink, K., Westberg, L., Eriksson, E., Adolfsson, R., & Nilsson, L. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929054475136 · Cited by 141
Dopamine Modulation of Membrane and Synaptic Properties of Interneurons in Rat Cerebral Cortex
Zhou, F.-M., & Hablitz, J. J. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.3.967 · Cited by 136
Interactions between prefrontal cortex and cerebellum revealed by trace eyelid conditioningPreprint
Kalmbach, B. E., Ohyama, T., Kreider, J. C., Riusech, F., & Mauk, M. D. (2009) · Learning & Memory · doi:10.1101/lm.1178309 · Cited by 142
Livingstone, P. D., Srinivasan, J., Kew, J. N. C., Dawson, L. A., Gotti, C., Moretti, M., Shoaib, M., & Wonnacott, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06613.x · Cited by 133
“Dopamine is a prominent modulator of PFC executive functions, including working memory and attention (Williams & Goldman-Rakic, 1995; Schultz, 2002; Floresco & Magyar, 2006).”
BackgroundKern, C. H., Stanwood, G. D., & Smith, D. R. (2009) · Synapse · doi:10.1002/syn.20736 · Cited by 136
Spatial working memory alters the efficacy of input to visual cortex
Merrikhi, Y., Clark, K., Albarran, E., Parsa, M., Zirnsak, M., Moore, T., & Noudoost, B. (2017) · Nature Communications · doi:10.1038/ncomms15041 · 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-citationGiakoumaki, S. G., Roussos, P., & Bitsios, P. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.82 · Cited by 136
Serotonin/dopamine interaction in memory formation
González‐Burgos, I., & Feria‐Velasco, A. (2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00928-x · Cited by 138
Holmes, A., Lachowicz, J. E., & Sibley, D. R. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.07.034 · Cited by 133
Mesocortical dopamine and HPA axis regulation: Role of laterality and early environment
Sullivan, R. M., & Dufresne, M. M. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.100 · Cited by 131
“…window of prefrontal DAergic function in numerous forms of learning and working memory, not only in primates (Sawaguchi and Goldman-Rakic, 1991; Williams and Goldman-Rakic, 1995), but also in various attentional and learning processes in rodents, including the extinction of conditioned fear…”
BackgroundThe Neuromodulatory System: A Framework for Survival and Adaptive Behavior in a Challenging World
Krichmar, J. L. (2008) · Adaptive Behavior · doi:10.1177/1059712308095775 · Cited by 132
FROST: A Distributed Neurocomputational Model of Working Memory Maintenance
Ashby, F. G., Ell, S. W., Valentin, V. V., & Casale, M. B. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/089892905774589271 · Cited by 132
“As Figure 1 shows, several single-unit recording studies have reported pFC cells whose firing increases at the beginning of the delay rather than during stimulus presentation ( Williams & Goldman-Rakic, 1995; Fuster, 1973; Fuster & Alexander, 1971).”
BackgroundLaminar and Cellular Distribution of Monoamine Receptors in Rat Medial Prefrontal Cortex
Santana, N., & Artigas, F. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00087 · Cited by 135
“This expression pattern may be relevant to understand the inverted U relationship between D1-R activation and working memory performance (Williams and Goldman-Rakic, 1995).”
BackgroundNeural activity in prefrontal cortex during copying geometrical shapes
Averbeck, B. B., Crowe, D. A., Chafee, M. V., & Georgopoulos, A. P. (2003) · Experimental Brain Research · doi:10.1007/s00221-003-1417-5 · Cited by 133
Theoretical neurobiology and schizophrenia
Friston, K. J. (1996) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a011573 · Cited by 129
Hochstadt, J., Nakano, H., LIEBERMAN, P. H., & Friedman, J. H. (2005) · Brain and Language · doi:10.1016/j.bandl.2005.10.011 · Cited by 134
Brake, W. G., Sullivan, R. M., & Gratton, A. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-14-05538.2000 · Cited by 131
The dopamine D4 receptor: biochemical and signalling properties
Rondou, P., Haegeman, G., & Craenenbroeck, K. V. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0293-y · Cited by 146
Weickert, T. W., Goldberg, T. E., Mishara, A. L., Apud, J. A., Kolachana, B. S., Egan, M. F., & Weinberger, D. R. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.08.012 · Cited by 130
Neurofeedback-mediated self-regulation of the dopaminergic midbrain
Sulzer, J. S., Sitaram, R., Blefari, M. L., Kollias, S., Birbaumer, N., Stephan, K. E., Luft, A. R., & Gassert, R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.115 · Cited by 129
“…(York, 1970), nucleus accumbens (Salamone and Correa, 2002), hippocampus (Rossato et al., 2009), amygdala (Wilson et al., 1994), subthalamic nucleus (Limousin et al., 1998) and prefrontal cortex (Williams and Goldman-Rakic, 1995) — all brain regions with presumed involvement in reward processing.”
BackgroundPostnatal alterations in dopaminergic markers in the human prefrontal cortex
Weickert, C. S., Webster, M. J., Gondipalli, P., Rothmond, D., Fatula, R. J., Herman, M. M., Kleinman, J. E., & Akil, M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.009 · Cited by 126
Dopamine modulates an mGluR5-mediated depolarization underlying prefrontal persistent activity
Sidiropoulou, K., Lu, F.-M., Fowler, M. A., Xiao, R., Phillips, C. W., Ozkan, E. D., Zhu, M. X., White, F. J., & Cooper, D. (2009) · Nature Neuroscience · doi:10.1038/nn.2245 · Cited by 131
Metadata
- Authors
- Williams, G. V., & Goldman-Rakic, P. S.
- Affiliations
- Yale University (US)
- ORCID
- Williams, Graham V.
- Venue
- Nature
- Published
- 1995-08
- Volume
- 376
- Issue
- 6541
- Pages
- 572-575
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2084007108
- Cited by
- 1,593
- References
- 42
- Citations by year
- 2026: 17 · 2025: 13 · 2024: 29 · 2023: 26 · 2022: 36 · 2021: 30 · 2020: 27 · 2019: 27 · 2018: 37 · 2017: 33 · 2016: 48 · 2015: 63 · 2014: 45 · 2013: 78 · 2012: 74
- FWCI
- 16.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- dopamine D1 receptor, working memory, prefrontal cortex, memory field, dopamine D1 receptor antagonist, synaptic modulation, excitatory synaptic input, iontophoresis, single-unit recording
- MeSH terms
- Animals, Haplorhini, Dose-Response Relationship, Drug, Iontophoresis, Memory, Neurons, Psychomotor Performance, Prefrontal Cortex, Receptors, Dopamine D1, Receptors, Dopamine D2
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