Evidence map›Paper›PMID 40826812›Full record

ArticleJournal of neurochemistry2025

Ropinirole Functions Through a Dopamine Receptor D2-Independent Mechanism to Ameliorate Amyotrophic Lateral Sclerosis Phenotypes in TARDBP-Mutant iPSC-Derived Motor Neurons.

Hirotsugu Asano, Tetsuya Kawaguchi, Chris Kato, Satoru Morimoto, Masato Yano, Maki Minaguchi, Daisuke Yasuda, Komei Fukushima, Hideyuki Okano

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

9 authors.

Hirotsugu AsanoDrug Discovery Research Department, K Pharma, Inc., Fujisawa-shi, Kanagawa, Japan.ORCID 0000-0001-7857-7879
Tetsuya KawaguchiDrug Discovery Research Department, K Pharma, Inc., Fujisawa-shi, Kanagawa, Japan.ORCID 0000-0003-1394-5129
Chris KatoKeio University Regenerative Medicine Research Center, Kawasaki-shi, Kanagawa, Japan.
Satoru MorimotoKeio University Regenerative Medicine Research Center, Kawasaki-shi, Kanagawa, Japan.
Masato YanoCore Research Facilities for Basic Science, Research Center for Medical Science, The Jikei University School of Medicine, Minato-ku, Tokyo, Japan.
Maki MinaguchiDrug Discovery Research Department, K Pharma, Inc., Fujisawa-shi, Kanagawa, Japan.
Daisuke YasudaDepartment of Pharmaceutical Sciences, Osaka Medical and Pharmaceutical University, Takatsuki-shi, Osaka, Japan.
Komei FukushimaDrug Discovery Research Department, K Pharma, Inc., Fujisawa-shi, Kanagawa, Japan.
Hideyuki OkanoDrug Discovery Research Department, K Pharma, Inc., Fujisawa-shi, Kanagawa, Japan.ORCID 0000-0001-7482-5935

Funding

Japan Agency for Medical Research and Development JP20H00485Japan Agency for Medical Research and Development JP21wm0425009Japan Agency for Medical Research and Development JP22bm0804003Japan Agency for Medical Research and Development JP22ek0109616Japan Agency for Medical Research and Development JP23bm1123046Japan Agency for Medical Research and Development JP23bm1423002Japan Society for the Promotion of Science JP21H05278Japan Society for the Promotion of Science JP22K15736
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease characterized by motor neuron (MN) degeneration. Ropinirole hydrochloride (ROPI), a dopamine receptor D2 (DRD2) agonist, was identified through phenotypic screening of MNs derived from patient-derived induced pluripotent stem cells (iPSCs) as a disease model and has emerged as a promising candidate drug for ALS treatment. The ROPALS trial, a phase I/IIa trial in patients with ALS, suggested the safety and efficacy of ROPI, albeit in a small sample size. Interestingly, a DRD2 antagonist and modulator only partially mitigated the suppressive effect of ROPI on the ALS phenotype, and the detailed mechanism of ROPI activity remains unclear. Therefore, in this study, we investigated whether the therapeutic effects of ROPI in ALS are dependent on DRD2. For this purpose, we generated DRD2-deficient iPSCs and showed that ROPI effectively reduced neuronal cell death, reactive oxygen species (ROS) production, and neuronal hyperexcitation, independently of DRD2. Further analyses revealed that ROPI corrected aberrant RNA splicing and restored the mRNA expression of mitochondrial proteins in a DRD2-independent manner. Our findings suggest that ROPI not only functions as a canonical DRD2 agonist but also has pleiotropic DRD2-independent effects, offering a novel avenue for treatment strategies that target multiple pathways involved in ALS pathology.

Indexed as

Amyotrophic Lateral SclerosisDNA-Binding ProteinsDopamine AgonistsIndolesInduced Pluripotent Stem CellsMotor NeuronsReceptors, Dopamine D2AnimalsCells, CulturedHumansMiceMutationPhenotypeReactive Oxygen SpeciesDNA-Binding ProteinsDopamine AgonistsIndolesReactive Oxygen SpeciesReceptors, Dopamine D2ropiniroleaberrant RNA splicingamyotrophic lateral sclerosisdopamine D2 receptorneuronal hyperexcitationropiniroleTARDBP

Identifiers

PMID40826812
PMCPMC12361731

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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.