Evidence map›Paper›PMID 26105137›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2016

Negative Allosteric Modulators Selective for The NR2B Subtype of The NMDA Receptor Impair Cognition in Multiple Domains.

Michael R Weed, Mark Bookbinder, Joseph Polino, Deborah Keavy, Rudolf N Cardinal, Jean Simmermacher-Mayer, Fu-ni L Cometa, Dalton King, Srinivasan Thangathirupathy, John E Macor and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Therapeutic potential of N-methyl-D-aspartate receptor modulators in psychiatry.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  6. A GlutamateThe Journal of pharmacology and experimental therapeutics · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. A GluN2B-Selective NMDAR Antagonist Reverses Synapse Loss and Cognitive Impairment Produced by the HIV-1 Protein Tat.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  13. Article
  14. Article
  15. Review
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

11 authors at 4 institutions in 5 countries.

Michael R WeedGenetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Mark BookbinderGenetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Joseph PolinoGenetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Deborah KeavyGenetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Rudolf N CardinalBehavioral and Clinical Neuroscience Institute, Department of Psychiatry, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-8751-5167
Jean Simmermacher-MayerPharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Fu-ni L CometaPharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Dalton KingDiscovery Chemistry, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Srinivasan ThangathirupathyDiscovery Chemistry, Biocon Bristol-Myers Squibb Research & Development Center, Bangalore, India.
John E MacorDiscovery Chemistry, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Linda J BristowGenetically Defined Diseases and Genomics, Bristol-Myers Squibb Company, Wallingford, CT, USA.
Bristol-Myers Squibb (Germany) · DEBristol-Myers Squibb (United States) · USBristol-Myers Squibb (India) · INUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antidepressant activity of N-methyl-D-aspartate (NMDA) receptor antagonists and negative allosteric modulators (NAMs) has led to increased investigation of their behavioral pharmacology. NMDA antagonists, such as ketamine, impair cognition in multiple species and in multiple cognitive domains. However, studies with NR2B subtype-selective NAMs have reported mixed results in rodents including increased impulsivity, no effect on cognition, impairment or even improvement of some cognitive tasks. To date, the effects of NR2B-selective NAMs on cognitive tests have not been reported in nonhuman primates. The current study evaluated two selective NR2B NAMs, CP101,606 and BMT-108908, along with the nonselective NMDA antagonists, ketamine and AZD6765, in the nonhuman primate Cambridge Neuropsychological Test Automated Battery (CANTAB) list-based delayed match to sample (list-DMS) task. Ketamine and the two NMDA NR2B NAMs produced selective impairments in memory in the list-DMS task. AZD6765 impaired performance in a non-specific manner. In a separate cohort, CP101,606 impaired performance of the nonhuman primate CANTAB visuo-spatial Paired Associates Learning (vsPAL) task with a selective impairment at more difficult conditions. The results of these studies clearly show that systemic administration of a selective NR2B NAM can cause transient cognitive impairment in multiple cognitive domains.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinAnimalsbeta-CyclodextrinsBromineCognitionCognition DisordersCohort StudiesDrug CombinationsExcitatory Amino Acid AntagonistsGlutamatesKetamineMacacaMagnesiumMaleMemory, Short-TermNeuropsychological Tests2-Hydroxypropyl-beta-cyclodextrinAZD6765beta-CyclodextrinsBromineDrug CombinationsExcitatory Amino Acid AntagonistsGlutamatesKetamineMagnesiumNR2B NMDA receptorPhenethylaminesPiperidinesPsychoverlanPyridinesReceptors, N-Methyl-D-Aspartatetraxoprodil mesylate

Identifiers

PMID26105137
PMCPMC5130132
OpenAlexW1508872668

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.