Evidence map›Paper›PMID 18003824›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2007

Somatodendritic release of glutamate regulates synaptic inhibition in cerebellar Purkinje cells via autocrine mGluR1 activation.

Ian C Duguid, Yuriy Pankratov, Guy W J Moss, Trevor G Smart

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.8field-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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Dendritic Release of Neurotransmitters.Comprehensive Physiology · 2016
    Review
  6. Article
  7. Article
  8. Review
  9. Multiple signalling modalities mediated by dendritic exocytosis of oxytocin and vasopressin.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  10. Transmembrane AMPAR regulatory protein γ-2 is required for the modulation of GABA release by presynaptic AMPARs.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  11. Article
  12. Article
  13. Cerebellar secretin modulates eyeblink classical conditioning.Learning & memory (Cold Spring Harbor, N.Y.) · 2014
    Article
  14. Cannabinoid receptors contribute to astroglial Ca²⁺-signalling and control of synaptic plasticity in the neocortex.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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 1 institution in 1 country.

Ian C DuguidDepartment of Pharmacology, University College London, London WC1E 6BT, United Kingdom.
Yuriy Pankratov
Guy W J Moss
Trevor G Smart
University College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D01817X/1Medical Research Council G0601529Wellcome Trust
6 · The paper itself

Abstract

In the cerebellum, the process of retrograde signaling via presynaptic receptors is important for the induction of short- and long-term changes in inhibitory synaptic transmission at interneuron-Purkinje cell (PC) synapses. Endocannabinoids, by activating presynaptic CB1 receptors, mediate a short-term decrease in inhibitory synaptic efficacy, whereas glutamate, acting on presynaptic NMDA receptors, induces a longer-latency sustained increase in GABA release. We now demonstrate that either low-frequency climbing fiber stimulation or direct somatic depolarization of Purkinje cells results in SNARE-dependent vesicular release of glutamate from the soma and dendrites of PCs. The activity-dependent release of glutamate caused the activation of postsynaptic metabotropic glutamate receptor 1 (mGluR1) on PC somatodendritic membranes, resulting in the cooperative release of endocannabinoids and an mGluR1-mediated slow membrane conductance. The activity of excitatory amino acid transporters regulated the spatial spread of glutamate and thus the extent of PC mGluR1 activation. We propose that activity-dependent somatodendritic glutamate release and autocrine activation of mGluR1 on PCs provides a powerful homeostatic mechanism to dynamically regulate inhibitory synaptic transmission in the cerebellar cortex.

Indexed as

Afferent PathwaysAnimalsAnimals, NewbornAutocrine CommunicationCannabinoid Receptor ModulatorsCerebellumDendritesElectric StimulationGlutamic AcidHomeostasisNeural InhibitionOrgan Culture TechniquesPurkinje CellsRatsRats, Sprague-DawleyReceptors, Metabotropic GlutamateCannabinoid Receptor ModulatorsGlutamic Acidmetabotropic glutamate receptor type 1Receptors, Metabotropic GlutamateSNARE Proteins

Identifiers

PMID18003824
PMCPMC6673325
OpenAlexW2071666600

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.