Evidence map›Paper›PMID 20180842›Full record

ArticleThe European journal of neuroscience2010

M-type channels selectively control bursting in rat dopaminergic neurons.

Guillaume Drion, Maxime Bonjean, Olivier Waroux, Jacqueline Scuvée-Moreau, Jean-Françis Liégeois, Terrence J Sejnowski, Rodolphe Sepulchre, Vincent Seutin

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Shaping the Action Potential in Dorsal Root and Trigeminal Ganglia Neurons: Relevance to Pain Mechanisms.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Review
  3. Rebound Bursting Selectively Enables Fast Dynamics in Dopamine Midbrain Neurons Projecting to the Dorsolateral Striatum.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  4. Article
  5. Voltage-gated potassium channels control extended access cocaine seeking: a role for nucleus accumbens astrocytes.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  6. Vascular mechanotransduction.Physiological reviews · 2023
    Review
  7. Chemical modulation of Kv7 potassium channels.RSC medicinal chemistry · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Mechanisms of cannabinoid CBEBioMedicine · 2019
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Selective targeting of M-type potassium KBritish journal of pharmacology · 2017
    Article
  17. Article
  18. Article
  19. Mechanisms for multiple activity modes of VTA dopamine neurons.Frontiers in computational neuroscience · 2015
    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

8 authors.

Guillaume DrionLaboratory of Pharmacology and GIGA Neurosciences, University of Liège, Belgium.
Maxime Bonjean
Olivier Waroux
Jacqueline Scuvée-Moreau
Jean-Françis Liégeois
Terrence J Sejnowski
Rodolphe Sepulchre
Vincent Seutin

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Midbrain dopaminergic neurons in the substantia nigra, pars compacta and ventral tegmental area are critically important in many physiological functions. These neurons exhibit firing patterns that include tonic slow pacemaking, irregular firing and bursting, and the amount of dopamine that is present in the synaptic cleft is much increased during bursting. The mechanisms responsible for the switch between these spiking patterns remain unclear. Using both in-vivo recordings combined with microiontophoretic or intraperitoneal drug applications and in-vitro experiments, we have found that M-type channels, which are present in midbrain dopaminergic cells, modulate the firing during bursting without affecting the background low-frequency pacemaker firing. Thus, a selective blocker of these channels, 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone dihydrochloride, specifically potentiated burst firing. Computer modeling of the dopamine neuron confirmed the possibility of a differential influence of M-type channels on excitability during various firing patterns. Therefore, these channels may provide a novel target for the treatment of dopamine-related diseases, including Parkinson's disease and drug addiction. Moreover, our results demonstrate that the influence of M-type channels on the excitability of these slow pacemaker neurons is conditional upon their firing pattern.

Indexed as

Action PotentialsAnimalsComputer SimulationDopamineKCNQ Potassium ChannelsMaleMesencephalonModels, NeurologicalNeuronsOrgan Culture TechniquesRatsRats, WistarDopamineKcnq4 protein, ratKCNQ Potassium Channels

Identifiers

PMID20180842
PMCPMC2861736

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.