Evidence map›Paper›PMID 29534526›Full record

ArticleInternational journal of molecular sciences2018

Peiminine Protects Dopaminergic Neurons from Inflammation-Induced Cell Death by Inhibiting the ERK1/2 and NF-κB Signalling Pathways.

Guangxin Chen, Juxiong Liu, Liqiang Jiang, Xin Ran, Dewei He, Yuhang Li, Bingxu Huang, Wei Wang, Dianfeng Liu, Shoupeng Fu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 51 citations in OpenAlex.

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  6. Peiminine inhibits myocardial injury and fibrosis after myocardial infarction in rats by regulating mitogen-activated protein kinase pathway.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2022
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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

10 authors at 1 institution in 1 country.

Guangxin ChenCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. cgxkc@outlook.com.
Juxiong LiuCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. juxiong@jlu.edu.cn.
Liqiang JiangCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. 17843105106@163.com.
Xin RanCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. ranxin21001x@163.com.
Dewei HeCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. m13144303829@163.com.
Yuhang LiCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. yhli9915@mails.jlu.edu.cn.
Bingxu HuangCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. huangbingxu16@mails.jlu.edu.cn.
Wei WangCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. wangwei@jlu.edu.cn.
Dianfeng LiuCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. liudf@jlu.edu.cn.
Shoupeng FuCollege of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China. fushoupeng@jlu.edu.cn.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroinflammation, characterized marked by microglial activation, plays a very important role in the pathogenesis of Parkinson's disease (PD). Upon activation, pro-inflammatory mediators are produced by microglia, triggering excessive inflammatory responses and ultimately damaging dopaminergic neurons. Therefore, the identification of agents that inhibit neuroinflammation may be an effective approach for developing novel treatments for PD. In this study, we sought to investigate whether peiminine protects dopaminergic neurons by inhibiting neuroinflammation. We evaluated the effects of peiminine on behavioural dysfunction, microglial activation and the loss of dopaminergic neurons in a rat model of lipopolysaccharide (LPS)-induced PD. BV-2 cells were pretreated with peiminine for 1 h and then stimulated with LPS for different times. Then, inflammatory responses and the related signalling pathways were analysed. Peiminine markedly attenuated behavioural dysfunction and inhibited the loss of dopaminergic neurons and microglial activation in the LPS-induced PD rat model. In BV-2 cells, peiminine significantly decreased LPS-induced expression of the pro-inflammatory mediators TNF-α, IL-6 and IL-1β, COX-2 and iNOS by inhibiting the phosphorylation of ERK1/2, AKT and NF-κB p65. Based on these results demonstrated that peiminine has a role in protecting dopaminergic neurons in the LPS-induced PD rat model by inhibiting neuroinflammation.

Indexed as

Signal TransductionAnimalsAnti-Inflammatory AgentsCell DeathCell LineCevanesCyclooxygenase 2Dopaminergic NeuronsFemaleInterleukinsLipopolysaccharidesMiceMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neuroprotective AgentsNF-kappa BAnti-Inflammatory AgentsCevanesCyclooxygenase 2InterleukinsLipopolysaccharidesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neuroprotective AgentsNF-kappa BNitric Oxide Synthase Type IIpeiminineProto-Oncogene Proteins c-aktTumor Necrosis Factor-alphaAKTERK1/2microgliaNF-κBParkinson’s diseasepeiminine

Identifiers

PMID29534526
PMCPMC5877682
OpenAlexW2789728673

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.