Evidence map›Paper›PMID 31440123›Full record

ArticleFrontiers in neuroscience2019

Therapeutic Effect of Modulating TREM-1 via Anti-inflammation and Autophagy in Parkinson's Disease.

Chien-Wei Feng, Nan-Fu Chen, Chun-Sung Sung, Hsiao-Mei Kuo, San-Nan Yang, Chien-Liang Chen, Han-Chun Hung, Bing-Hung Chen, Zhi-Hong Wen, Wu-Fu Chen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Article
  9. Article
  10. Review
  11. Article
  12. HIV-1 Tat Upregulates TREM1 Expression in Human Microglia.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  13. Article
  14. The role of TREM2 in Alzheimer's disease: from the perspective of Tau.Frontiers in cell and developmental biology · 2023
    Review
  15. Review
  16. Development of an extended half-life GM-CSF fusion protein for Parkinson's disease.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  17. Article
  18. Observational
  19. Article
  20. Article
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 7 institutions in 2 countries.

Chien-Wei FengNational Museum of Marine Biology & Aquarium, Pingtung, Taiwan.
Nan-Fu ChenDivision of Neurosurgery, Department of Surgery, Kaohsiung Armed Forces General Hospital, Kaohsiung City, Taiwan.
Chun-Sung SungDepartment of Anesthesiology, Taipei Veterans General Hospital, Taipei, Taiwan.
Hsiao-Mei KuoDepartment of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung City, Taiwan.
San-Nan YangDepartment of Pediatrics, E-Da Hospital, Kaohsiung City, Taiwan.
Chien-Liang ChenDivision of Nephrology, Kaohsiung Veterans General Hospital, Kaohsiung City, Taiwan.
Han-Chun HungDepartment of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung City, Taiwan.
Bing-Hung ChenDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung City, Taiwan.
Zhi-Hong WenDepartment of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung City, Taiwan.
Wu-Fu ChenDepartment of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung City, Taiwan.
National Sun Yat-sen University · TWE-Da Hospital · TWKaohsiung Armed Forces General Hospital · TWKaohsiung Medical University Chung-Ho Memorial Hospital · TWKaohsiung Veterans General Hospital · TWNational Museum of Marine Biology and Aquarium · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is one of the most common age-related neurodegenerative diseases, and neuroinflammation has been identified as one of its key pathological characteristics. Triggering receptors expressed on myeloid cells-1 (TREM-1) amplify the inflammatory response and play a role in sepsis and cancer. Recent studies have demonstrated that the attenuation of TREM-1 activity produces cytoprotective and anti-inflammatory effects in macrophages. However, no study has examined the role of TREM-1 in neurodegeneration. We showed that LP17, a synthetic peptide blocker of TREM-1, significantly inhibited the lipopolysaccharide (LPS)-induced upregulation of proinflammatory cascades of inducible nitric oxide synthase (iNOS), cyclooxygenase-2, and nuclear factor-kappa B. Moreover, LP17 enhanced the LPS-induced upregulation of autophagy-related proteins such as light chain-3 and histone deacetylase-6. We also knocked down TREM-1 expression in a BV2 cell model to further confirm the role of TREM-1. LP17 inhibited 6-hydroxydopamine-induced locomotor deficit and iNOS messenger RNA expression in zebrafish. We also observed therapeutic effects of LP17 administration in 6-hydroxydopamine-induced PD syndrome using a rat model. These data suggest that the attenuation of TREM-1 could ameliorate neuroinflammatory responses in PD and that this neuroprotective effect might occur via the activation of autophagy and anti-inflammatory pathways.

Indexed as

autophagyneuroinflammationParkinson’s diseaseratTREM-1zebrafish

Identifiers

PMID31440123
PMCPMC6691936
OpenAlexW2958564001

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.