Evidence map›Paper›PMID 31002755›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2019

Genetic silencing of striatal CaV1.3 prevents and ameliorates levodopa dyskinesia.

Kathy Steece-Collier, Jennifer A Stancati, Nicholas J Collier, Ivette M Sandoval, Natosha M Mercado, Caryl E Sortwell, Timothy J Collier, Fredric P Manfredsson

Open access · hybridAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2019. 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
1.3field-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

27 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
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  5. Disease-modifying, multidimensional efficacy of putaminal CaMolecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  6. Review
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  11. The L-type calcium channel CaV1.3: A potential target for cancer therapy.Journal of cellular and molecular medicine · 2024
    Review
  12. Article
  13. Article
  14. Downregulation of striatal CaNeurobiology of disease · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Pathway-Specific Remodeling of Thalamostriatal Synapses in a Mouse Model of Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2022
    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

8 authors at 1 institution in 1 country.

Kathy Steece-CollierDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Jennifer A StancatiDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Nicholas J CollierDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Ivette M SandovalDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Natosha M MercadoDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Caryl E SortwellDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.ORCID 0000-0003-2571-6753
Timothy J CollierDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Fredric P ManfredssonDepartment of Translational Science & Molecular Medicine, College of Human Medicine, Michigan State University, Grand Rapids, MI, USA.
Grand Rapids Community College · US

Funding

Genetic Silencing of Striatal CaV1.3 Calcium Channels as a Potent Antidyskinetic Therapy for PDR01NS110398 · NINDS · MICHIGAN STATE UNIVERSITY · PI Jeffrey H Kordower, Fredric Manfredsson · 2018 to 2026
$5.3M
Striatal Nurr1 activity facilitates the dyskinetic state: A novel therapeutic targetR21NS098079 · NINDS · MICHIGAN STATE UNIVERSITY · PI MANFREDSSON, FREDRIC · 2016 to 2017
$441k
Striatal CaV1.3 Calcium Channels: An Overlooked Antidyskinetic Target for PDR21NS090107 · NINDS · MICHIGAN STATE UNIVERSITY · PI STEECE-COLLIER, KATHY · 2015 to 2016
$384k
NINDS NIH HHS R01 NS110398NINDS NIH HHS R21 NS090107NINDS NIH HHS R21 NS098079
6 · The paper itself

Abstract

backgroundLevodopa-induced dyskinesias are an often debilitating side effect of levodopa therapy in Parkinson's disease. Although up to 90% of individuals with PD develop this side effect, uniformly effective and well-tolerated antidyskinetic treatment remains a significant unmet need. The pathognomonic loss of striatal dopamine in PD results in dysregulation and disinhibition of striatal CaV1.3 calcium channels, leading to synaptopathology that appears to be involved in levodopa-induced dyskinesias. Although there are clinically available drugs that can inhibit CaV1.3 channels, they are not adequately potent and have only partial and transient impact on levodopa-induced dyskinesias.

methodsTo provide unequivocal target validation, free of pharmacological limitations, we developed a CaV1.3 shRNA to provide high-potency, target-selective, mRNA-level silencing of striatal CaV1.3 channels and examined its ability to impact levodopa-induced dyskinesias in severely parkinsonian rats.

resultsWe demonstrate that vector-mediated silencing of striatal CaV1.3 expression in severely parkinsonian rats prior to the introduction of levodopa can uniformly and completely prevent induction of levodopa-induced dyskinesias, and this antidyskinetic benefit persists long term and with high-dose levodopa. In addition, this approach is capable of ameliorating preexisting severe levodopa-induced dyskinesias. Importantly, motoric responses to low-dose levodopa remained intact in the presence of striatal CaV1.3 silencing, indicating preservation of levodopa benefit without dyskinesia liability. DISCUSSION: The current data provide some of the most profound antidyskinetic benefit reported to date and suggest that genetic silencing of striatal CaV1.3 channels has the potential to transform treatment of individuals with PD by allowing maintenance of motor benefit of levodopa in the absence of the debilitating levodopa-induced dyskinesia side effect. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Adrenergic AgentsAnimalsAntiparkinson AgentsCalcium ChannelsDisease Models, AnimalDyskinesia, Drug-InducedGreen Fluorescent ProteinsLevodopaLuminescent AgentsMedial Forebrain BundleNeostriatumOxidopamineParkinsonian DisordersRatsRNA InterferenceRNA, Small InterferingAdrenergic AgentsAntiparkinson AgentsCacna1d protein, ratCalcium ChannelsGreen Fluorescent ProteinsLevodopaLuminescent AgentsOxidopamineRNA, Small InterferingTyrosine 3-Monooxygenaseadeno-associated virus (AAV)CaV1.3 channelsdyskinesialevodopastriatum

Identifiers

PMID31002755
PMCPMC6563183
OpenAlexW2937043410

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.