Evidence map›Paper›PMID 25314304›Full record

ArticlePloS one2014

Pyrroloquinoline quinone (PQQ) inhibits lipopolysaccharide induced inflammation in part via downregulated NF-κB and p38/JNK activation in microglial and attenuates microglia activation in lipopolysaccharide treatment mice.

Chongfei Yang, Lifeng Yu, Lingbo Kong, Rui Ma, Juliang Zhang, Qingsheng Zhu, Jinyu Zhu, Dingjun Hao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-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

29 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

8 authors at 3 institutions in 1 country.

Chongfei YangInstitute of Orthopaedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Lifeng YuInstitute of Orthopaedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Lingbo KongHong-Hui Hospital, Xi'an Jiaotong University College of Medicine, Xi'an, China.
Rui MaDepartment of Anesthesiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Juliang ZhangInstitute of Orthopaedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Qingsheng ZhuInstitute of Orthopaedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jinyu ZhuInstitute of Orthopaedic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Dingjun HaoHong-Hui Hospital, Xi'an Jiaotong University College of Medicine, Xi'an, China.
Air Force Medical University · CNXi'an Honghui Hospital · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic strategies designed to inhibit the activation of microglia may lead to significant advancement in the treatment of most neurodegenerative diseases. Pyrroloquinoline quinone (PQQ) is a naturally occurring redox cofactor that acts as an essential nutrient, antioxidant, and has been reported to exert potent immunosuppressive effects. In the present study, the anti-inflammatory effects of PQQ was investigated in LPS treated primary microglia cells. Our observations showed that pretreatment with PQQ significantly inhibited the production of NO and PGE2 and suppressed the expression of pro-inflammatory mediators such as iNOS, COX-2, TNF-a, IL-1b, IL-6, MCP-1 and MIP-1a in LPS treated primary microglia cells. The nuclear translocation of NF-κB and the phosphorylation level of p65, p38 and JNK MAP kinase pathways were also inhibited by PQQ in LPS stimulated primary microglia cells. Further a systemic LPS treatment acute inflammation murine brain model was used to study the suppressive effects of PQQ against neuroinflammation in vivo. Mice treated with PQQ demonstrated marked attenuation of neuroinflammation based on Western blotting and immunohistochemistry analysis of Iba1-against antibody in the brain tissue. Indicated that PQQ protected primary cortical neurons against microglia-mediated neurotoxicity. These results collectively suggested that PQQ might be a promising therapeutic agent for alleviating the progress of neurodegenerative diseases associated with microglia activation.

Indexed as

AnimalsAnti-Inflammatory AgentsBrainCalcium-Binding ProteinsCells, CulturedCyclooxygenase 2DinoprostoneDrug Evaluation, PreclinicalEnzyme ActivationFemaleGene ExpressionInflammation MediatorsJNK Mitogen-Activated Protein KinasesLipopolysaccharidesMAP Kinase Signaling SystemMice, Inbred C57BLAif1 protein, mouseAnti-Inflammatory AgentsCalcium-Binding ProteinsCyclooxygenase 2DinoprostoneInflammation MediatorsJNK Mitogen-Activated Protein KinasesLipopolysaccharidesMicrofilament Proteinsp38 Mitogen-Activated Protein KinasesPQQ CofactorPtgs2 protein, mouseRela protein, mouseTranscription Factor RelA

Identifiers

PMID25314304
PMCPMC4196908
OpenAlexW1972646454

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.