Evidence map›Paper›PMID 21734865›Full record

ArticleFrontiers in cellular neuroscience2011

GABA(A) Receptors: Post-Synaptic Co-Localization and Cross-Talk with Other Receptors.

Amulya Nidhi Shrivastava, Antoine Triller, Werner Sieghart

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.0field-weighted citation impact, top 31% 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

28 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. GABACells · 2022
    Article
  6. Article
  7. GABAergic CaMKIIα+ Amygdala Output Attenuates Pain and Modulates Emotional-Motivational Behavior via Parabrachial Inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  8. Significance of GABAInternational journal of molecular sciences · 2021
    Review
  9. Advances in novel molecular targets for antidepressants.Progress in neuro-psychopharmacology & biological psychiatry · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. GABAFrontiers in neuroscience · 2020
    Article
  15. Article
  16. Photopotentiation of the GABAProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Presynaptic αThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  19. Alterations in GABAFrontiers in cellular neuroscience · 2019
    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

3 authors at 2 institutions in 2 countries.

Amulya Nidhi ShrivastavaDepartment of Biochemistry and Molecular Biology, Center for Brain Research, Medical University of Vienna Vienna, Austria.
Antoine Triller
Werner Sieghart
Institut de Biologie de l'École Normale Supérieure · FRMedical University of Vienna · AT

Funding

Austrian Science Fund FWF W 1205
6 · The paper itself

Abstract

γ-Aminobutyric acid type A receptors (GABA(A)Rs) are the major inhibitory neurotransmitter receptors in the central nervous system, and importantly contribute to the functional regulation of the nervous system. Several studies in the last few decades have convincingly shown that GABA can be co-localized with other neurotransmitters in the same synapse, and can be co-released with these neurotransmitters either from the same vesicles or from different vesicle pools. The co-released transmitters may act on post-synaptically co-localized receptors resulting in a simultaneous activation of both receptors. Most of the studies investigating such co-activation observed a reduced efficacy of GABA for activating GABA(A)Rs and thus, a reduced inhibition of the post-synaptic neuron. Similarly, in several cases activation of GABA(A)Rs has been reported to suppress the response of the associated receptors. Such a receptor cross-talk is either mediated via a direct coupling between the two receptors or via the activation of intracellular signaling pathways and is used for fine tuning of inhibition in the nervous system. Recently, it was demonstrated that a direct interaction of different receptors might already occur in intracellular compartments and might also be used to specifically target the receptors to the cell membrane. In this article, we provide an overview on such cross-talks between GABA(A)Rs and several other neurotransmitter receptors and briefly discuss their possible physiological and clinical importance.

Indexed as

cross-talkGABAARionotropic receptorsmetabotropic receptorstargeting

Identifiers

PMID21734865
PMCPMC3123775
OpenAlexW2072464305

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.