Evidence map›Paper›PMID 42003734›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

Indirect Striatal Projection Neurons Drive a D2 Receptor-Dependent Pathway to Dyskinesia and Dystonia.

Laura Andreoli, Teodor Nyman, Elena Espa, Johan Jakobsson, Osama F Elabi, Maria Angela Cenci

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Laura AndreoliBasal Ganglia Pathophysiology Group, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Teodor NymanBasal Ganglia Pathophysiology Group, Department of Experimental Medical Science, Lund University, Lund, Sweden.ORCID https://orcid.org/0009-0008-5060-2006
Elena EspaBasal Ganglia Pathophysiology Group, Department of Experimental Medical Science, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0002-1321-226X
Johan JakobssonMolecular Neurogenetics Laboratory, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Osama F ElabiBasal Ganglia Pathophysiology Group, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Maria Angela CenciBasal Ganglia Pathophysiology Group, Department of Experimental Medical Science, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0003-2216-2900

Funding

Lundbeck Foundation R336-2020-1035Swedish Brain Foundation FO2022-0293Swedish Government Funding for Clinical Research ALF-43301Vetenskapsrådet 2020-02696Vetenskapsrådet 2024-02491
6 · The paper itself

Abstract

backgroundL-DOPA-induced dyskinesia is attributed to opposite activity changes mediated by D1 and D2 dopamine receptors in the two striatal output pathways. Whereas the causal role of direct-pathway D1 receptors is well established, the specific involvement of indirect-pathway D2 receptors in dopaminergic dyskinesias has remained elusive.

objectivesWe used conditional knockout approaches in mice to determine whether indirect-pathway D2 receptors causally contribute to dyskinetic and dystonic responses to dopaminergic agents.

methodsStudies were conducted in mice with unilateral 6-hydroxydopamine lesions of the nigrostriatal pathway receiving subchronic treatments with L-DOPA or D2/D1-selective agonists. A conditional knockout of indirect-pathway D2 receptors was produced either through the entire striatum (double-transgenic Adora2a-Cre/Drd2

resultsThe severity of L-DOPA-induced abnormal involuntary movements and dystonia was halved in both knockout models compared with control mice, whereas the treatment effect on normal motor behaviors was either not reduced or improved. All dyskinetic and dystonic features induced by the D2-selective receptor agonist sumanirole were completely abolished, whereas those induced by the D1-class agonist SKF38393 were largely unaffected. Using phosphorylated ribosomal protein S6 as an activity marker, we detected a treatment-induced recruitment of prototypical parvalbumin-positive neurons in the external globus pallidus (a target of indirect-pathway projections). This effect was inhibited in both knockout models.

conclusionsWe provide experimental evidence that indirect-pathway D2 receptors significantly contribute to the expression of dyskinesia during L-DOPA treatment and mediate D2 agonist-dependent dystonic features. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Corpus StriatumDyskinesia, Drug-InducedDystoniaNeuronsReceptors, Dopamine D2AnimalsAntiparkinson AgentsDisease Models, AnimalDopamine AgonistsLevodopaMaleMiceMice, KnockoutMice, TransgenicOxidopamineReceptors, Dopamine D1Antiparkinson AgentsDopamine AgonistsLevodopaOxidopamineReceptors, Dopamine D1Receptors, Dopamine D2dopamine agonistslevodopa‐induced dyskinesiasParkinson's diseasepathophysiologyrodent models

Identifiers

PMID42003734
PMCPMC13388010

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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.