Evidence map›Paper›PMID 26738476›Full record

ReviewAnnual review of pharmacology and toxicology2016

Targeting Prefrontal Cortical Systems for Drug Development: Potential Therapies for Cognitive Disorders.

Amy F T Arnsten, Min Wang

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of pharmacology and toxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.2field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 52 citations in OpenAlex.

  1. Trial
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  3. Effects of Epothilone D on Social Defeat Stress-induced Changes in Microtubule-related and Endoplasmic Reticulum Stress Protein Expression.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2025
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  8. Opportunities and limitations of genetically modified nonhuman primate models for neuroscience research.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Amy F T ArnstenDepartment of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510; email: Amy.arnsten@yale.edu , Min.wang@yale.edu.
Min WangDepartment of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06510; email: Amy.arnsten@yale.edu , Min.wang@yale.edu.
Yale University · US

Funding

Highly evolved brain circuits in primates: molecular vulnerabilities for diseaseDP1AG047744 · NIA · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 2013 to 2017
$4.1M
Nicotinic Receptor Influences on Neuronal Physiology in Dorsolateral Prefrontal CR01MH093354 · NIMH · YALE UNIVERSITY · PI WANG, MIN · 2012 to 2020
$3.8M
Potential mGluR treatment of age-related cognitive declineR01AG043430 · NIA · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 2013 to 2017
$3.2M
mGluR2/3 influences in primate prefrontal cortex: potential for therapeuticsR01MH100064 · NIMH · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 2014 to 2016
$1.5M
NIA NIH HHS DP1 AG047744NIA NIH HHS DP1AG047744-01NIA NIH HHS R01 AG043430NIA NIH HHS R01AG043430-01A1NIMH NIH HHS R01 MH093354NIMH NIH HHS R01MH09335401A1NIMH NIH HHS R01 MH100064NIMH NIH HHS R01MH100064-01A1
6 · The paper itself

Abstract

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.

Indexed as

AnimalsCognitionCognition DisordersHumansNeuronsPrefrontal CortexacetylcholineAlzheimer's diseasedopaminenorepinephrineschizophrenia

Identifiers

PMID26738476
PMCPMC4734124
OpenAlexW2134555567

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.