Evidence map›Paper›PMID 40414345›Full record

ArticleJournal of advanced research2026

Targeting the bile acid receptor TGR5 with Gentiopicroside to activate Nrf2 antioxidant signaling and mitigate Parkinson's disease in an MPTP mouse model.

Ying Gao, Xiuling Tang, Jingyue Yao, Ting Sun, Yue Chen, Caiyan Cheng, Jingcheng Yang, Bao Wang, An Liu, Le Yang and 1 more

Abstract read
In one paragraph

Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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  8. Quality Evaluation and Antioxidant Activity of CultivatedMolecules (Basel, Switzerland) · 2026
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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

11 authors.

Ying GaoPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Xiuling TangPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Jingyue YaoPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Ting SunPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Yue ChenPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Caiyan ChengPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Jingcheng YangPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
Bao WangDepartment of Neurosurgery, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China.
An LiuPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China. Electronic address: anran1222@163.com.
Le YangPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China. Electronic address: yanglefmmu@163.com.
Minggao ZhaoPrecision Pharmacy & Drug Development Center, Department of Pharmacy, Tangdu Hospital, The Fourth Military Medical University, Xi'an 710038 Shaanxi, People's Republic of China. Electronic address: minggao@fmmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionParkinson's disease (PD) is a common neurodegenerative disorder characterized by classical symptoms including bradykinesia, rest tremor and rigidity. Oxidative stress and mitochondrial dysfunction are recognized as pivotal factors in PD progression. Gentiopicroside (GPS), a secoiridoid derived from Gentiana manshurica Kitagawa, exhibits antioxidant and mitophagy induction properties. Nonetheless, the effects and mechanisms by which GPS mitigates neurodegeneration in PD remain to be thoroughly elucidated.

objectivesThe goal of this study was to investigate the neuroprotective effects and mechanisms of GPS in PD models.

methodsWe established the MPTP/MPP

resultsGPS significantly attenuated dopaminergic (DAergic) neuron loss and restored motor function in the MPTP-induced PD mouse model. Whole-genome RNA sequencing and subsequent mechanistic investigations revealed that GPS enhanced the expression and facilitated nuclear entry of factor erythroid-related 2-factor 2 (Nrf2), and reduced oxidative stress and mitochondrial dysfunction stimulated by neurotoxin. Additionally, GPS could target TGR5 and prevent its downregulation in PD model. TGR5's silencing or inhibition weakened the neuroprotective effect of GPS and blocked GPS-mediated activation of Nrf2 antioxidant signaling in PD model. Moreover, the therapeutic effect of GPS in mitigating motor deficits and neurodegeneration was also abolished in Tgr5 knockout mice.

conclusionThese findings collectively indicated that GPS targeted TGR5 to activate Nrf2 antioxidant signaling and ultimately ameliorated the pathological progression of PD.

Indexed as

AntioxidantsIridoid GlucosidesNF-E2-Related Factor 2Parkinson DiseaseReceptors, G-Protein-CoupledAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLMice, KnockoutNeuroprotective AgentsOxidative StressSignal TransductionAntioxidantsgentiopicrosideGpbar1 protein, mouseIridoid GlucosidesNeuroprotective AgentsNfe2l2 protein, mouseNF-E2-Related Factor 2Receptors, G-Protein-CoupledGentiopicrosideNrf2Oxidative stressParkinson’s diseaseTGR5

Identifiers

PMID40414345
PMCPMC12869198

What Socratic 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 Socratic graph.