Evidence map›Paper›PMID 36691817›Full record

ArticleCNS neuroscience & therapeutics2023

Artemisinin exerts a protective effect in the MPTP mouse model of Parkinson's disease by inhibiting microglial activation via the TLR4/Myd88/NF-KB pathway.

Jing Lv, Jing Zhu, Peihan Wang, Tongyu Liu, Jiang Yuan, Huan Yin, Yiran Lan, Qiang Sun, Zhifeng Zhang, Guoda Ding and 4 more

Open access · goldFull text read
In one paragraph

Article in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Dihydroartemisinin Modulates Enteric Glial Cell Heterogeneity to Alleviate Colitis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  8. Review
  9. Article
  10. Review
  11. 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

14 authors at 2 institutions in 1 country.

Jing LvDepartment of Neurology, Graduate Training Base of Jinzhou Medical University, Affiliated Hospital of Hubei Medical College, Taihe Hospital, Shiyan, China.ORCID 0000-0002-5048-3982
Jing ZhuInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Peihan WangInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Tongyu LiuInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Jiang YuanDepartment of Neurology, Taihe Hospital of Hubei University of Medicine, Shiyan, China.
Huan YinSinopharm Dongfeng General Hospital, Hubei University of Medicine, Shiyan, China.
Yiran LanInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Qiang SunDepartment of Neurology, Taihe Hospital of Hubei University of Medicine, Shiyan, China.
Zhifeng ZhangInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Guoda DingDepartment of Neurology, Graduate Training Base of Jinzhou Medical University, Affiliated Hospital of Hubei Medical College, Taihe Hospital, Shiyan, China.
Chenxi ZhouDepartment of Neurology, Graduate Training Base of Jinzhou Medical University, Affiliated Hospital of Hubei Medical College, Taihe Hospital, Shiyan, China.
Huajie WangInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Zihan WangInstitute of Neuroscience, Hubei University of Medicine, Shiyan, China.
Yunfu WangDepartment of Neurology, Graduate Training Base of Jinzhou Medical University, Affiliated Hospital of Hubei Medical College, Taihe Hospital, Shiyan, China.
Hubei University of Medicine · CNTaihe Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsWe performed cell and animal experiments to explore the therapeutic effect of artemisinin on Parkinson's disease (PD) and the TLR4/Myd88 signaling pathway.

methodsC57 mice were randomly divided into the blank, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced and artemisinin-treated groups. Clinical symptoms, the number of dopaminergic (DAergic) neurons in the substantia nigra, and microglial cell activation were compared among the three groups. Subsequently, BV-2 cell activation and TLR4/Myd88 pathway component expression were compared among the blank, MPP

resultsBehavioral symptoms were improved, the number of DAergic neurons in the substantia nigra of the midbrain was increased, and microglial cell activation was decreased in artemisinin-treated MPTP-induced PD model mice compared with control-treated MPTP-induced PD model mice (p < 0.05). The cell experiments revealed that artemisinin treatment reduced MPP

conclusionArtemisinin may reduce damage to DAergic neurons in a PD mouse model by decreasing microglial activation through the TLR4-mediated MyD88-dependent signaling pathway. However, this finding cannot explain the relationship between microglia and DAergic neurons.

Indexed as

ArtemisininsParkinson Disease1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAdaptor Proteins, Signal TransducingAnimalsDisease Models, AnimalDopaminergic NeuronsMiceMice, Inbred C57BLMicrogliaMyeloid Differentiation Factor 88NF-kappa BSubstantia NigraToll-Like Receptor 41-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAdaptor Proteins, Signal TransducingArtemisininsMyd88 protein, mouseMyeloid Differentiation Factor 88NF-kappa BTlr4 protein, mouseToll-Like Receptor 4artemisinininflammationmicrogliaParkinson's diseasetoll-like receptor 4

Identifiers

PMID36691817
PMCPMC10018080
OpenAlexW4317829405

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read59
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.