Evidence map›Paper›PMID 19923300›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Functional heterogeneity at dopamine release sites.

James A Daniel, Sally Galbraith, Lorraine Iacovitti, Andrea Abdipranoto, Bryce Vissel

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. A fluorescent nanosensor paint detects dopamine release at axonal varicosities with high spatiotemporal resolution.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Article
  8. Spatial and temporal scales of dopamine transmission.Nature reviews. Neuroscience · 2021
    Review
  9. Review
  10. Mechanisms and regulation of dopamine release.Current opinion in neurobiology · 2019
    Review
  11. Altered Synaptic Vesicle Release and CaFrontiers in molecular neuroscience · 2018
    Article
  12. Article
  13. Article
  14. Fast phasic release properties of dopamine studied with a channel biosensor.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  15. Article
  16. Epitope-tagged dopamine transporter knock-in mice reveal rapid endocytic trafficking and filopodia targeting of the transporter in dopaminergic axons.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012
    Article
  17. Article
  18. Article
  19. Review
  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

5 authors at 4 institutions in 3 countries.

James A DanielNeuroscience Program, Garvan Institute of Medical Research, Sydney, New South Wales 2010, Australia.
Sally Galbraith
Lorraine Iacovitti
Andrea Abdipranoto
Bryce Vissel
Faculty (United Kingdom) · GBGarvan Institute of Medical Research · AUThomas Jefferson University · USUNSW Sydney · AU

Funding

STUDIES OF PURIFIED DOPAMINE NEURONSR01NS032519 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI IACOVITTI, LORRAINE · 1994 to 2007
$2.1M
PURIFIED DOPAMINE NEURONSR55NS032519 · NINDS · THOMAS JEFFERSON UNIVERSITY · PI IACOVITTI, LORRAINE · 1998 to 1998
–
NINDS NIH HHS NS32519-15NINDS NIH HHS R01 NS032519
6 · The paper itself

Abstract

Although drugs used to treat several neurological diseases are presumed to target synapses that secrete dopamine (DA), relatively little is known about synaptic vesicle (SV) release mechanisms at single DA synapses. We found that the relative probability of release (Pr) varied between individual DA synapses. Furthermore, DA terminals generally exhibited lower Pr than glutamatergic hippocampal (Hpc) terminals, suggesting that DA release is less reliable than the release of glutamate. Our mathematical model of fluorescence loss shows that Pr is regulated by two independent and heterogeneous elements. First, the size of the recycling SV pool regulates Pr. Second, Pr is also independently regulated by additional factors, which are reflected in the time constant of FM 1-43 destaining, tau. We found that the observed difference in Pr between Hpc and DA neurons results because the recycling SV pool is smaller in DA neurons than in Hpc neurons. However, tau does not vary between these two neuron populations. We also identified a population of functional nonsynaptic boutons in DA axons, which are not associated with a postsynaptic element and which are not functionally different from boutons that formed conventional synapses. Our work provides a new approach to the study of SV exocytosis in DA neurons and shows that synaptic terminals of DA neurons are functionally heterogeneous and differ from excitatory terminals in terms of Pr.

Indexed as

AnimalsAnimals, NewbornCells, CulturedDopamineFemaleFluorescenceMiceModels, NeurologicalSynaptic VesiclesDopamine

Identifiers

PMID19923300
PMCPMC2871952
OpenAlexW2046812017

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.