Evidence map›Paper›PMID 21644997›Full record

ReviewJournal of neurochemistry2011

Advances in understanding the peptide neurotransmitter NAAG and appearance of a new member of the NAAG neuropeptide family.

Joseph H Neale, Rafal T Olszewski, Daiying Zuo, Karolina J Janczura, Caterina P Profaci, Kaleen M Lavin, John C Madore, Tomasz Bzdega

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of neurochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. mNSCs overexpressingiScience · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. The potential ofPsychopharmacology · 2021
    Review
  18. Article
  19. Article
  20. Evidence of NAAG-family tripeptide NAAGJournal of neurochemistry · 2021
    Article
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

8 authors at 2 institutions in 2 countries.

Joseph H NealeDepartment of Biology, Georgetown University, Washington, District of Columbia 20057, USA. nealej@georgetown.edu
Rafal T Olszewski
Daiying Zuo
Karolina J Janczura
Caterina P Profaci
Kaleen M Lavin
John C Madore
Tomasz Bzdega
Georgetown University · USShenyang Pharmaceutical University · CN

Funding

NAAG PEPTIDASE AND NEURONAL FUNCTIONR01NS038080 · NINDS · GEORGETOWN UNIVERSITY · PI NEALE, JOSEPH H · 2000 to 2008
$2.4M
Neurochemical and Behavioral Activity of NAAG in Animal Models of SchizophreniaR01MH079983 · NIMH · GEORGETOWN UNIVERSITY · PI NEALE, JOSEPH H · 2008 to 2011
$1.4M
Howard Hughes Medical InstituteNIMH NIH HHS MH79983NIMH NIH HHS R01 MH079983NINDS NIH HHS NS38080NINDS NIH HHS R01 NS038080
6 · The paper itself

Abstract

A substantial body of data was reported between 1984 and 2000 demonstrating that the neuropeptide N-acetylaspartylglutamate (NAAG) not only functions as a neurotransmitter but also is the third most prevalent transmitter in the mammalian nervous system behind glutamate and GABA. By 2005, this conclusion was validated further through a series of studies in vivo and in vitro. The primary enzyme responsible for the inactivation of NAAG following its synaptic release had been cloned, characterized and knocked out. Potent inhibitors of this enzyme were developed and their efficacy has been extensively studied in a series of animal models of clinical conditions, including stroke, peripheral neuropathy, traumatic brain injury, inflammatory and neuropathic pain, cocaine addiction, and schizophrenia. Considerable progress also has been made in defining further the mechanism of action of these peptidase inhibitors in elevating synaptic levels of NAAG with the consequent inhibition of transmitter release via the activation of pre-synaptic metabotropic glutamate receptor 3 by this peptide. Very recent discoveries include identification of two different nervous system enzymes that mediate the synthesis of NAAG from N-acetylaspartate and glutamate and the finding that one of these enzymes also mediates the synthesis of a second member of the NAAG family of neuropeptides, N-acetylaspartylglutamylglutamate.

Indexed as

AnimalsAstrocytesBrain InjuriesDipeptidesGlutamate Carboxypeptidase IIHumansHyperalgesiaNeuralgiaNeuropeptidesNeurotransmitter AgentsPeripheral Nervous System DiseasesProtease InhibitorsSchizophreniaSubstance-Related DisordersDipeptidesGlutamate Carboxypeptidase IIisospaglumic acidN-acetyl-aspartyl-glutamyl-glutamic acidNeuropeptidesNeurotransmitter AgentsProtease Inhibitors

Identifiers

PMID21644997
PMCPMC3137677
OpenAlexW1729884812

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.