Cited by 313Neurotransmitter Receptor Influence on BehaviorSchizophrenia research and treatmentNeuroscience and Neuropharmacology Research

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The Physiological Role of 5-HT2AReceptors in Working Memory

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Williams, Graham V., Rao, Srinivas G., Goldman-Rakic, Patricia S.·2002·The Journal of Neuroscience

DOI 10.1523/jneurosci.22-07-02843.2002PMC PMC6758292

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Abstract

Dorsolateral prefrontal cortex has an essential role in the cognitive process of working memory, dysfunction of which is considered to be a core deficit in schizophrenia. Although this cortical region is densely innervated with 5-HT 2A receptors to which atypical antipsychotic drugs bind with high affinity, little is known of the influence of this serotonin receptor subtype on prefrontal function. We addressed this issue by examining the effects of iontophoresis of selective receptor ligands on prefrontal neurons possessing spatially tuned delay activity, or “memory fields,” in monkeys performing a delayed-response task. Memory fields of putative pyramidal cells were attenuated by iontophoresis of 5-HT 2A antagonists, which primarily produced a reduction in delay activity for preferred target locations. Conversely, 5-HT 2A stimulation by α-methyl-5-HT or 5-HT itself, accentuated the spatial tuning of these neurons by producing a modest increase in activity for preferred target locations and/or a reduction in activity for nonpreferred locations. The agonist effects could be reversed by the selective antagonist MDL100,907, and were dose-dependent, such that high levels attenuated spatial tuning by profoundly reducing delay activity. A role for feedforward inhibitory circuitry in these effects was supported by the finding that 5-HT 2A blockade also attenuated the memory fields of putative interneurons. We conclude that prefrontal 5-HT 2A receptors have a hitherto unrecognized role in the cognitive function of working memory, which involves actions at both excitatory and inhibitory elements within local circuitry.

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Practical Nonparametric Statistics
Groggel, D. J., & Conover, W. J. (2000) · Technometrics · doi:10.2307/1271101 · Cited by 11,076
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
Self-citation
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Self-citation
Statistical 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
Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia
Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,025
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex
McCormick, D. A., Connors, B. W., Lighthall, J. W., & Prince, D. A. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.782 · Cited by 1,935
Statistical Analysis of Circular Data
Fisher, N. I. (1993) · Cambridge University Press eBooks · doi:10.1017/cbo9780511564345 · Cited by 1,826
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
Self-citation
Dissociable Deficits in the Decision-Making Cognition of Chronic Amphetamine Abusers, Opiate Abusers, Patients with Focal Damage to Prefrontal Cortex, and Tryptophan-Depleted Normal Volunteers Evidence for Monoaminergic Mechanisms
Rogers, R. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(98)00091-8 · Cited by 1,101

Show all 87 references

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Authors: Williams, G. V., Rao, S. G., & Goldman-Rakic, P. S.
Affiliations: Yale University (US)
ORCID: Williams, Graham V.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2002-04-01
Volume: 22
Issue: 7
Pages: 2843-2854
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.22-07-02843.2002
PMC: PMC6758292
OpenAlex: W1635746382
Cited by: 311
References: 87
Citations by year: 2026: 6 · 2025: 6 · 2024: 13 · 2023: 7 · 2022: 7 · 2021: 9 · 2020: 8 · 2019: 5 · 2018: 10 · 2017: 10 · 2016: 14 · 2015: 14 · 2014: 13 · 2013: 12 · 2012: 10
FWCI: 6.76
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Institute of Mental Health (MH 44866, R37MH038546, P50MH044866)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: 5-HT2A receptor, serotonin, working memory, dorsolateral prefrontal cortex, delay activity, memory field, pyramidal neurons, interneurons, feedforward inhibition, schizophrenia, atypical antipsychotics, alpha-methyl-5-HT, spatial tuning, delayed response task, iontophoresis
MeSH terms: Action Potentials, Animals, Cognition, Fixation, Ocular, Iontophoresis, Ligands, Macaca mulatta, Male, Memory, Short-Term, Neurons, Photic Stimulation, Reaction Time, Receptors, Serotonin, Saccades, Serotonin Antagonists, Serotonin Receptor Agonists, Prefrontal Cortex, Pyramidal Cells, Receptor, Serotonin, 5-HT2A

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The Physiological Role of 5-HT2AReceptors in Working Memory

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