Evidence map›Paper›PMID 18537642›Full record

ReviewCNS & neurological disorders drug targets2008

Ionotropic glutamate receptors & CNS disorders.

Derek Bowie

Open access · greenAbstract readReview
In one paragraph

Review in CNS & neurological disorders drug targets, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

93 citing papers in PubMed, 209 citations in OpenAlex.

  1. Article
  2. Article
  3. HAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  4. Selective Modulation of the GluN2B/C/D ContainingACS medicinal chemistry letters · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Temperature Sensitive Glutamate Gating of AMPA-subtype iGluRs.bioRxiv : the preprint server for biology · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Conserved gene signatures shared amongFrontiers in molecular biosciences · 2023
    Article
  17. Review
  18. Review
  19. Structural insights into function of ionotropic glutamate receptors.Biochemistry (Moscow) Supplement. Series A, Membrane and cell biology · 2022
    Article
  20. Article

33 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

1 author at 1 institution in 1 country.

Derek BowieDepartment of Pharmacology and Therapeutics, McGill University, Montreal, Québec, Canada. derek.bowie@mcgill.ca
McGill University · CA

Funding

Properties of AMPA and Kainate receptorsR01MH062144 · NIMH · EMORY UNIVERSITY · PI IUVONE, P. MICHAEL · 2001 to 2005
$1.2M
NIMH NIH HHS R01 MH062144
6 · The paper itself

Abstract

Disorders of the central nervous system (CNS) are complex disease states that represent a major challenge for modern medicine. Although aetilogy is often unknown, it is established that multiple factors such as defects in genetics and/or epigenetics, the environment as well as imbalance in neurotransmitter receptor systems are all at play in determining an individual's susceptibility to disease. Gene therapy is currently not available and therefore, most conditions are treated with pharmacological agents that modify neurotransmitter receptor signaling. Here, I provide a review of ionotropic glutamate receptors (iGluRs) and the roles they fulfill in numerous CNS disorders. Specifically, I argue that our understanding of iGluRs has reached a critical turning point to permit, for the first time, a comprehensive re-evaluation of their role in the cause of disease. I illustrate this by highlighting how defects in AMPA receptor (AMPAR) trafficking are important to fragile X mental retardation and ectopic expression of kainate receptor (KAR) synapses contributes to the pathology of temporal lobe epilepsy. Finally, I discuss how parallel advances in studies of other neurotransmitter systems may allow pharmacologists to work towards a cure for many CNS disorders rather than developing drugs to treat their symptoms.

Indexed as

AnimalsCentral Nervous System DiseasesEpilepsyFragile X SyndromeHumansKainic Acid ReceptorsReceptors, AMPAReceptors, GlutamateReceptors, NeurotransmitterKainic Acid ReceptorsReceptors, AMPAReceptors, GlutamateReceptors, Neurotransmitter

Identifiers

PMID18537642
PMCPMC2662616
OpenAlexW1980970141

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.