Evidence map›Paper›PMID 17303246›Full record

ReviewPharmacology & therapeutics2007

Adrenergic pharmacology and cognition: focus on the prefrontal cortex.

Brian P Ramos, Amy F T Arnsten

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 317 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
317citing papers in PubMed, 3 pooled it
9.0field-weighted citation impact, top 1% 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

317 citing papers in PubMed, 3 syntheses or guidelines pooled it, 639 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Treatment of Post-Traumatic Stress Disorders with the Alpha-1 Adrenergic Antagonist Prazosin.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2017
    Pooled it
  4. Trial
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  9. Guanfacine extended-release for cannabis use disorder: a pilot feasibility trial.The American journal of drug and alcohol abuse · 2020
    Trial
  10. Effects of clonidine on MMN and P3a amplitude in schizophrenia patients on stable medication.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Trial
  11. Trial
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  13. Trial
  14. Article
  15. Review
  16. Article
  17. Crosstalk of noradrenergic CaCell communication and signaling : CCS · 2026
    Article
  18. Article
  19. Article
  20. Article

257 more citing papers are in PubMed but not listed here.

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.

Brian P RamosDepartment Neurobiology, Yale Medical School, New Haven, CT 06520-8001, USA.
Amy F T Arnsten
Yale University · US

Funding

COGNITIVE LOSS WITH AGE--ROLE OF CORTICAL CATECHOLAMINESR37AG006036 · NIA · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 1998 to 2007
$3.0M
Ionic and Second Messanger Basis of Stress-Induced Prefrontal Dysfunction (#2 ofRL1AA017536 · NIAAA · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 2007 to 2011
$1.8M
COGNITIVE LOSS WITH AGE: ROLE OF CORTICAL CATECHOLAMINESR01AG006036 · NIA · YALE UNIVERSITY · PI ARNSTEN, AMY F.T. · 1986 to 1997
–
NIAAA NIH HHS RL1 AA017536NIA NIH HHS AG06036NIA NIH HHS R01 AG006036NIA NIH HHS R37 AG006036
6 · The paper itself

Abstract

Norepinephrine (NE) has widespread projections throughout the brain, and thus, is ideally positioned to orchestrate neural functions based on arousal state. For example, NE can increase "signal/noise" ratio in the processing of sensory stimuli, and can enhance long-term memory consolidation in the amygdala and hippocampus through actions at alpha-1 and beta adrenoceptors. Over the last 20 years, NE has also been shown to play a powerful role in regulating the working memory and attention functions of the prefrontal cortex (PFC). Moderate levels of NE released under control conditions strengthen prefrontal cortical functions via actions at post-synaptic alpha-2A adrenoceptors with high affinity for NE, while high levels of NE release during stress impair PFC cortical functions via alpha-1 and possibly beta-1 receptors with lower affinity for NE. Thus, levels of NE determine whether prefrontal cortical or posterior cortical systems control our behavior and thought. Understanding these receptor mechanisms has led to new intelligent treatments for neuropsychiatric disorders associated with PFC dysfunction.

Indexed as

CognitionHumansLocus CoeruleusMemoryMental DisordersNorepinephrinePrefrontal CortexReceptors, Adrenergic, alphaReceptors, Adrenergic, betaNorepinephrineReceptors, Adrenergic, alphaReceptors, Adrenergic, beta

Identifiers

PMID17303246
PMCPMC2151919
OpenAlexW1985339809

What OpenQuestion holds

Textmetadata
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.