Evidence map›Paper›PMID 40382635›Full record

ArticleJournal of neuroinflammation2025

Rebamipide (Mucosta®), a clinically approved drug, alleviates neuroinflammation and dopaminergic neurodegeneration in a Parkinson's disease model.

Hye-Sun Lim, Jinyoung Park, Eunjeong Kim, Wonhwa Lee, Hwi-Yeol Yun, Seung Hoon Lee, Gunhyuk Park

Abstract read
In one paragraph

Article in Journal of neuroinflammation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
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  5. [Regulatory mechanisms of post-translational modifications in inflammasome signaling: a review].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2026
    Review
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  8. Article
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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

7 authors.

Hye-Sun LimHerbal Medicine Resources Research Center, Korea Institute of Oriental Medicine, 111 Geonjae-Ro, Naju-Si, Jeollanam-Do, 58245, Republic of Korea.
Jinyoung ParkDepartment of Chemistry, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Eunjeong KimDepartment of Biology, KNU G-LAMP Research Center, KNU Institute of Basic Sciences, BK21 FOUR KNU Creative BioResearch Group, College of Natural Sciences, Kyungpook National University, Daegu, 41566, Republic of Korea.
Wonhwa LeeDepartment of MetaBioHealth, SKKU Institute for Convergence, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Hwi-Yeol YunCollege of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.
Seung Hoon LeeDepartment of Biochemistry, Research Institute for Medical Science, Chungnam National University School of Medicine, 282 Munhwa-Ro, Jung-Gu, Daejeon, 35015, Republic of Korea.
Gunhyuk ParkHerbal Medicine Resources Research Center, Korea Institute of Oriental Medicine, 111 Geonjae-Ro, Naju-Si, Jeollanam-Do, 58245, Republic of Korea. gpark@kiom.re.kr.

Funding

Korea Institute for Advancement of Technology RS-2024-00434342Korea Institute of Oriental Medicine KSN1823320 and KSN2511030National Research Foundation of Korea RS-2024-00352796
6 · The paper itself

Abstract

backgroundParkinson's disease (PD) is characterized by dopaminergic neuron loss, neuroinflammation, and motor dysfunction. PD is a multifactorial disease, with neuroinflammation driven by NLRP3 inflammasome activation representing an important component of its pathological progression. Therefore, we aimed to evaluate the therapeutic potential of rebamipide (Mucosta®), a clinically approved anti-inflammatory agent, in PD by targeting the NLRP3 inflammasome. Specifically, we examined the effects of rebamipide on neuroinflammation, dopaminergic neuron preservation, and motor deficits using BV2 microglia cells and a 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced mouse model. MAIN BODY: Rebamipide alleviated microglial activation and downstream neuroinflammation by suppressing the NLRP3-NEK7 interaction, resulting in dopaminergic neuron protection in the MPTP-induced PD model. Rebamipide downregulated IL-1β levels in BV2 microglia cells treated with α-synuclein and MPP

conclusionConsidering its established clinical use, this study supports repurposing rebamipide for treating PD and other NLRP3 inflammasome-driven neuroinflammatory diseases.

Indexed as

AlanineDopaminergic NeuronsNeuroinflammatory DiseasesParkinsonian DisordersQuinolonesAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLMicrogliaMolecular Docking SimulationNeuroprotective AgentsNLR Family, Pyrin Domain-Containing 3 ProteinAlanineNeuroprotective AgentsNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseQuinolonesrebamipideMPTPNeuroinflammationNLRP3 inflammasomeParkinson’s diseaseRebamipide

Identifiers

PMID40382635
PMCPMC12085015

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.