Evidence map›Paper›PMID 25806702›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2015

Imaging in vivo glutamate fluctuations with [(11)C]ABP688: a GLT-1 challenge with ceftriaxone.

Eduardo R Zimmer, Maxime J Parent, Antoine Leuzy, Antonio Aliaga, Arturo Aliaga, Luc Moquin, Esther S Schirrmacher, Jean-Paul Soucy, Ivan Skelin, Alain Gratton and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

  1. Testing PET-[Imaging neuroscience (Cambridge, Mass.) · 2024
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  2. Review
  3. Article
  4. Article
  5. Article
  6. Measuring the effects of ketamine on mGluR5 using [Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Article
  7. A Review of Molecular Imaging of Glutamate Receptors.Molecules (Basel, Switzerland) · 2020
    Review
  8. Article
  9. Effect of (Z)-isomer content on [European journal of nuclear medicine and molecular imaging · 2019
    Article
  10. Molecular Imaging of mGluR5 Availability with [Cellular and molecular neurobiology · 2019
    Article
  11. Article
  12. Article
  13. Review
  14. New targets for rapid antidepressant action.Progress in neurobiology · 2017
    Review
  15. [Nature neuroscience · 2017
    Article
  16. Article
  17. Article
  18. Metabotropic glutamate receptor 5 - a promising target in drug development and neuroimaging.European journal of nuclear medicine and molecular imaging · 2016
    Review
  19. Article
  20. 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

12 authors at 3 institutions in 2 countries.

Eduardo R Zimmer1] Translational Neuroimaging Laboratory (TNL), McGill Center for Studies in Aging, Douglas Mental Health University Institute, Verdun, Quebec, Canada [2] Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, McGill University, Montreal, Quebec, Canada [3] Department of Biochemistry, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, RS, Brazil.
Maxime J Parent1] Translational Neuroimaging Laboratory (TNL), McGill Center for Studies in Aging, Douglas Mental Health University Institute, Verdun, Quebec, Canada [2] Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, McGill University, Montreal, Quebec, Canada.
Antoine Leuzy1] Translational Neuroimaging Laboratory (TNL), McGill Center for Studies in Aging, Douglas Mental Health University Institute, Verdun, Quebec, Canada [2] Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, McGill University, Montreal, Quebec, Canada.
Antonio AliagaMontreal Neurological Institute (MNI), Montreal, Quebec, Canada.
Arturo AliagaTranslational Neuroimaging Laboratory (TNL), McGill Center for Studies in Aging, Douglas Mental Health University Institute, Verdun, Quebec, Canada.
Luc MoquinDepartment of Psychiatry, Douglas Hospital Research Centre, McGill University, Montreal, Quebec, Canada.
Esther S SchirrmacherMontreal Neurological Institute (MNI), Montreal, Quebec, Canada.
Jean-Paul SoucyMontreal Neurological Institute (MNI), Montreal, Quebec, Canada.
Ivan SkelinMontreal Neurological Institute (MNI), Montreal, Quebec, Canada.
Alain GrattonDepartment of Psychiatry, Douglas Hospital Research Centre, McGill University, Montreal, Quebec, Canada.
Serge GauthierAlzheimer's Disease Research Unit, McGill Centre for Studies in Aging, McGill University, Montreal, Quebec, Canada.
Pedro Rosa-Neto1] Translational Neuroimaging Laboratory (TNL), McGill Center for Studies in Aging, Douglas Mental Health University Institute, Verdun, Quebec, Canada [2] Alzheimer's Disease Research Unit, McGill Centre for Studies in Aging, McGill University, Montreal, Quebec, Canada [3] Montreal Neurological Institute (MNI), Montreal, Quebec, Canada.
Douglas Mental Health University Institute · CAMontreal Neurological Institute and Hospital · CAMcGill University · CA

Funding

Canadian Institutes of Health Research MOP-11-51-31
6 · The paper itself

Abstract

Molecular imaging offers unprecedented opportunities for investigating dynamic changes underlying neuropsychiatric conditions. Here, we evaluated whether [(11)C]ABP688, a positron emission tomography (PET) ligand that binds to the allosteric site of the metabotropic glutamate receptor type 5 (mGluR5), is sensitive to glutamate fluctuations after a pharmacological challenge. For this, we used ceftriaxone (CEF) administration in rats, an activator of the GLT-1 transporter (EAAT2), which is known to decrease extracellular levels of glutamate. MicroPET [(11)C]ABP688 dynamic acquisitions were conducted in rats after a venous injection of either saline (baseline) or CEF 200 mg/kg (challenge). Binding potentials (BP(ND)) were obtained using the simplified reference tissue method. Between-condition statistical parametric maps indicating brain regions showing the highest CEF effects guided placement of microdialysis probes for subsequent assessment of extracellular levels of glutamate. The CEF administration increased [(11)C]ABP688 BP(ND) in the thalamic ventral anterior (VA) nucleus bilaterally. Subsequent microdialysis assessment revealed declines in extracellular glutamate concentrations in the VA. The present results support the concept that availability of mGluR5 allosteric binding sites is sensitive to extracellular concentrations of glutamate. This interesting property of mGluR5 allosteric binding sites has potential applications for assessing the role of glutamate in the pathogenesis of neuropsychiatric conditions.

Indexed as

Positron-Emission TomographyAnimalsCarbon RadioisotopesCeftriaxoneExcitatory Amino Acid Transporter 2Glutamic AcidOximesPyridinesRatsRats, Sprague-DawleyReceptor, Metabotropic Glutamate 5Thalamus3-(6-methylpyridin-2-ylethynyl)cyclohex-2-enone-O-methyloximeCarbon RadioisotopesCeftriaxoneExcitatory Amino Acid Transporter 2Glutamic AcidOximesPyridinesReceptor, Metabotropic Glutamate 5

Identifiers

PMID25806702
PMCPMC4640271
OpenAlexW2047737185

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.