The DOI matches its Crossref record; 138 of the 138 references it cites were found in a registry or an index.
Targeting Prefrontal Cortical Systems for Drug Development: Potential Therapies for Cognitive Disorders
Open accessAbstract
Medications to treat cognitive disorders are increasingly needed, yet researchers have had few successes in this challenging arena. Cognitive abilities in primates arise from highly evolved N-methyl-d-aspartate (NMDA) receptor circuits in layer III of the dorsolateral prefrontal cortex. These circuits have unique modulatory needs that can differ from the layer V neurons that predominate in rodents, but they offer multiple therapeutic targets. Cognitive improvement often requires low doses that enhance the pattern of information held in working memory, whereas higher doses can produce nonspecific changes that obscure information. Identifying appropriate doses for clinical trials may be helped by assessments in monkeys and by flexible, individualized dose designs. The use of guanfacine (Intuniv) for prefrontal cortical disorders was based on research in monkeys, supporting this approach. Coupling our knowledge of higher primate circuits with the powerful methods now available in drug design will help create effective treatments for cognitive disorders.
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“Guanfacine, a specific α2-AR antagonist, has been used to treat cognitive disorders linked to PFC dysfunction 251.”
From Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications (2022) · cites this paper as [251]
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“The rostral and dorsomedial aspects of the PFC also play important roles in social cognition, including so-called theory of mind, the ability to think about what another person must be thinking (19, 20).”
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Yan, Z., & Rein, B. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01092-3 · Cited by 300
“Guanfacine, a speci fi c α 2-AR antagonist, has been used to treat cognitive disorders linked to PFC dysfunction [251].”
MethodRole of Prefrontal Persistent Activity in Working Memory
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Metadata
- Authors
- Arnsten, A. F. T., & Wang, M.
- Affiliations
- Yale University (US)
- Venue
- Annual Review of Pharmacology and Toxicology
- Publisher
- Annual Reviews
- Published
- 2016-01-06
- Volume
- 56
- Issue
- 1
- Pages
- 339-360
- ISSN
- 0362-1642 (ISSN-L)
- 1545-4304
- PMC
- PMC4734124
- OpenAlex
- W2134555567
- Cited by
- 50
- References
- 138
- Citations by year
- 2024: 5 · 2023: 1 · 2021: 4 · 2020: 10 · 2019: 6 · 2018: 15 · 2017: 7 · 2016: 2
- FWCI
- 1.09
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Annual Review of Pharmacology and Toxicology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (DP1AG047744, R01AG043430)
- National Institute of Mental Health (R01MH093354, R01MH100064)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- cognitive disorders, prefrontal cortex, NMDA receptor, dorsolateral prefrontal cortex, working memory, guanfacine, dose-response relationship, nonhuman primate model, drug development, cognitive enhancement
- MeSH terms
- Animals, Cognition, Cognition Disorders, Humans, Neurons, Prefrontal Cortex
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