Evidence map›Paper›PMID 23469183›Full record

ArticlePloS one2013

Membrane properties of striatal direct and indirect pathway neurons in mouse and rat slices and their modulation by dopamine.

Henrike Planert, Thomas K Berger, Gilad Silberberg

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

99 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. Article
  3. Distinct forms of dopamine transmission control locomotion and learning.bioRxiv : the preprint server for biology · 2026
    Article
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  12. An anatomical substrate of credit assignment in reinforcement learning.bioRxiv : the preprint server for biology · 2025
    Article
  13. Ventral striatal astrocytes contribute to reinforcement learning.bioRxiv : the preprint server for biology · 2025
    Article
  14. Article
  15. Article
  16. Striatal Dopamine Actions and Movement: Inferences from Parkinson Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Haploinsufficiency ofThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article

39 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Henrike PlanertDepartment of Neuroscience, Karolinska Institute, Stockholm, Sweden. Henrike.Planert@ki.se
Thomas K Berger
Gilad Silberberg
Charité - Universitätsmedizin Berlin · DEKarolinska Institutet · SEUniversity of California, Berkeley · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

D1 and D2 receptor expressing striatal medium spiny neurons (MSNs) are ascribed to striatonigral ("direct") and striatopallidal ("indirect") pathways, respectively, that are believed to function antagonistically in motor control. Glutamatergic synaptic transmission onto the two types is differentially affected by Dopamine (DA), however, less is known about the effects on MSN intrinsic electrical properties. Using patch clamp recordings, we comprehensively characterized the two pathways in rats and mice, and investigated their DA modulation. We identified the direct pathway by retrograde labeling in rats, and in mice we used transgenic animals in which EGFP is expressed in D1 MSNs. MSNs were subjected to a series of current injections to pinpoint differences between the populations, and in mice also following bath application of DA. In both animal models, most electrical properties were similar, however, membrane excitability as measured by step and ramp current injections consistently differed, with direct pathway MSNs being less excitable than their counterparts. DA had opposite effects on excitability of D1 and D2 MSNs, counteracting the initial differences. Pronounced changes in AP shape were seen in D2 MSNs. In direct pathway MSNs, excitability increased across experimental conditions and parameters, and also when applying DA or the D1 agonist SKF-81297 in presence of blockers of cholinergic, GABAergic, and glutamatergic receptors. Thus, DA induced changes in excitability were D1 R mediated and intrinsic to direct pathway MSNs, and not a secondary network effect of altered synaptic transmission. DAergic modulation of intrinsic properties therefore acts in a synergistic manner with previously reported effects of DA on afferent synaptic transmission and dendritic processing, supporting the antagonistic model for direct vs. indirect striatal pathway function.

Indexed as

AnimalsBenzazepinesCell MembraneCorpus StriatumDopamineDopamine AgonistsDopamine D2 Receptor AntagonistsExcitatory Postsynaptic PotentialsGreen Fluorescent ProteinsMaleMiceMicrotomyNeuroanatomical Tract-Tracing TechniquesNeuronsPatch-Clamp TechniquesRatsBenzazepinesDopamineDopamine AgonistsDopamine D2 Receptor Antagonistsenhanced green fluorescent proteinGreen Fluorescent ProteinsReceptors, Dopamine D1Receptors, Dopamine D2SK&F 81297

Identifiers

PMID23469183
PMCPMC3585935
OpenAlexW2068401524

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.