Evidence map›Paper›PMID 42486828›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2026

[CHIR99021 alleviates neuroinflammation in a mouse model of Parkinson's disease by inhibiting the GSK-3β/NF-κB pathway].

Kelin Shi, Xiaochuan Qi, Shixiang Xu, Yuanyuan Gao, Mingzhe Fang, Juncheng Hu, Chunjing Wang, Changqing Liu, Yu Guo

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Kelin ShiAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Xiaochuan QiAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Shixiang XuAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Yuanyuan GaoAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Mingzhe FangAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Juncheng HuAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Chunjing WangAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Changqing LiuAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.
Yu GuoAnhui Engineering Research Center for Neural Regeneration Technology and Medical New Materials, Bengbu Medical University, Bengbu 233000, China.

Funding

National Natural Science Foundation of China 82371382
6 · The paper itself

Abstract

objectivesTo investigate the effect of CHIR99021 for improving neuroinflammation in a mouse model of Parkinson's disease (PD) and the role of the GSK-3β/NF-κB pathway in mediating this effect.

methodsIn the cell experiment, induced SH-SY5Y cells were pretreated with 3 μmol/L CHIR99021 for 2 h prior to MPP+ treatment. In a male C57BL/6 mouse model of MPTP-induced PD, the effect of intraperitoneal injection of CHIR99021 for 7 days on motor function of the mice were assessed using behavioral tests. Western blotting and immunofluorescence staining were used to detect the changes in the GSK-3β/NF-κB pathway, NLRP3 inflammasome and autophagy in both SH-SY5Y cells and the mouse models.

resultsMPP+-treated SH-SY5Y cells showed significantly downregulated expression of p-GSK-3β protein and upregulated expressions of p-NF-κB p65, ASC, NLPR3, and caspase-1, and these changes were obviously attenuated by pretreatment with CHIR99021. Compared with normal mice, the PD mouse models showed significantly decreased motor function and reduced TH neurons in the brain with lowered expression of p-GSK-3β, increased expression of p-NF-κB p65 (Ser536), and upregulated ASC, NLPR3, and caspase-1 expressions. Treatment with CHIR99021 significantly increased the expression of p-GSK-3β, and reduced the expression of p-NF‑κB p65 (Ser536), ASC, NLPR3, and caspase-1.

conclusionsCHIR99021 inhibits the GSK-3β/NF‑κB signaling pathway to improve motor function of PD mice, reduce neuroinflammation, and activate autophagy to maintain the homeostasis of intracellular environment, suggesting that targeting GSK-3β, a potential multifunctional therapeutic target, can simultaneously regulate multiple key pathological links in PD.

Indexed as

Glycogen Synthase Kinase 3 betaNF-kappa BParkinson DiseasePyridinesPyrimidinesAnimalsCell Line, TumorDisease Models, AnimalHumansInflammasomesMaleMiceMice, Inbred C57BLNeuroinflammatory DiseasesNLR Family, Pyrin Domain-Containing 3 ProteinSignal TransductionChir 99021Glycogen Synthase Kinase 3 betaInflammasomesNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPyridinesPyrimidinesCHIR99021GSK-3βneuroinflammationNF-κBParkinson's disease

Identifiers

PMID42486828
PMCPMC13391561

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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.