Evidence map›Paper›PMID 25225106›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2014

Cannabinoid receptors contribute to astroglial Ca²⁺-signalling and control of synaptic plasticity in the neocortex.

Seyed Rasooli-Nejad, Oleg Palygin, Ulyana Lalo, Yuriy Pankratov

Open access · bronzeAbstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Astroglial CBGlia · 2025
    Article
  3. The effects of cannabinoids on the kidney.Acta physiologica (Oxford, England) · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Electrophysiological In Vitro Study of Long-Range Signal Transmission by Astrocytic Networks.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Modulation of P2XPhysiological reports · 2022
    Article
  15. A requirement for astrocyte IPFrontiers in cellular neuroscience · 2022
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

Seyed Rasooli-NejadSchool of Life Sciences, University of Warwick, Coventry, UK.
Oleg PalyginSchool of Life Sciences, University of Warwick, Coventry, UK.
Ulyana LaloSchool of Life Sciences, University of Warwick, Coventry, UK.
Yuriy PankratovSchool of Life Sciences, University of Warwick, Coventry, UK y.pankratov@warwick.ac.uk.
Google (United States) · USUniversity of Warwick · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K009192/1
6 · The paper itself

Abstract

Communication between neuronal and glial cells is thought to be very important for many brain functions. Acting via release of gliotransmitters, astrocytes can modulate synaptic strength. The mechanisms underlying ATP release from astrocytes remain uncertain with exocytosis being the most intriguing and debated pathway. We have demonstrated that ATP and d-serine can be released from cortical astrocytes in situ by a SNARE-complex-dependent mechanism. Exocytosis of ATP from astrocytes can activate post-synaptic P2X receptors in the adjacent neurons, causing a downregulation of synaptic and extrasynaptic GABA receptors in cortical pyramidal neurons. We showed that release of gliotransmitters is important for the NMDA receptor-dependent synaptic plasticity in the neocortex. Firstly, induction of long-term potentiation (LTP) by five episodes of theta-burst stimulation (TBS) was impaired in the neocortex of dominant-negative (dn)-SNARE mice. The LTP was rescued in the dn-SNARE mice by application of exogenous non-hydrolysable ATP analogues. Secondly, we observed that weak sub-threshold stimulation (two TBS episodes) became able to induce LTP when astrocytes were additionally activated via CB-1 receptors. This facilitation was dependent on activity of ATP receptors and was abolished in the dn-SNARE mice. Our results strongly support the physiological relevance of glial exocytosis for glia-neuron communications and brain function.

Indexed as

Adenosine TriphosphateAnimalsAstrocytesCalcium SignalingMiceMice, TransgenicMicroscopy, FluorescenceNeocortexNeuronal PlasticityPatch-Clamp TechniquesReceptors, CannabinoidSerineSNARE ProteinsAdenosine TriphosphateReceptors, CannabinoidSerineSNARE Proteinsd-serineendocannabinoidglia–neuron interactionLTPsynaptic currentvesicular release

Identifiers

PMID25225106
PMCPMC4173298
OpenAlexW1988203397

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.