Evidence map›Paper›PMID 28750089›Full record

ArticlePloS one2017

A synthetic cationic antimicrobial peptide inhibits inflammatory response and the NLRP3 inflammasome by neutralizing LPS and ATP.

Lan-Hui Li, Tz-Chuen Ju, Chih-Yu Hsieh, Wei-Chih Dong, Wan-Tze Chen, Kuo-Feng Hua, Wei-Jung Chen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

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  15. Poly-Arginine Peptide-18 (R18) Reduces Brain Injury and Improves Functional Outcomes in a Nonhuman Primate Stroke Model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
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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

7 authors at 4 institutions in 1 country.

Lan-Hui LiDepartment of Laboratory Medicine, Lisen, Chinese Medicine and Kunming Branch, Taipei City Hospital, Taipei, Taiwan.
Tz-Chuen JuDepartment of Nursing, St. Mary's Junior College of Medicine, Nursing and Management, Ilan, Taiwan.
Chih-Yu HsiehDepartment of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.
Wei-Chih DongDepartment of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.
Wan-Tze ChenDepartment of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.
Kuo-Feng HuaDepartment of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.ORCID http://orcid.org/0000-0001-8436-8299
Wei-Jung ChenDepartment of Biotechnology and Animal Science, National Ilan University, Ilan, Taiwan.
National Ilan University · TWTri-Service General Hospital · TWMackay Junior College of Medicine, Nursing and Management · TWTaipei City Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are one of the most important defense mechanisms against bacterial infections in insects, plants, non-mammalian vertebrates, and mammals. In the present study, a class of synthetic AMPs was evaluated for anti-inflammatory activity. One cationic AMP, GW-A2, demonstrated the ability to inhibit the expression levels of nitric oxide (NO), inducible NO synthase (iNOS), cyclooxygenase-2 (COX-2), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) in lipopolysaccharide (LPS)-activated macrophages. GW-A2 reduced LPS-induced increases in the phosphorylation of mitogen-activated protein kinase and protein kinase C-α/δ and the activation of NF-κB. GW-A2 also inhibited NLRP3 inflammasome activation induced by LPS and ATP. Furthermore, in the mice injected with LPS, GW-A2 reduced (1) the concentration of IL-1β, IL-6 and TNF-α in the serum; (2) the concentration of TNF-α in the peritoneal lavage; (3) the expression levels of iNOS, COX-2 and NLRP3 in the liver and lung; (4) the infiltration of polymorphonuclear neutrophils in the liver and lung. The underlying mechanisms for the anti-inflammatory activity of GW-A2 were found to be partially due to LPS and ATP neutralization. These results provide insights into how GW-A2 inhibits inflammation and the NLRP3 inflammasome and provide a foundation for the design of rational therapeutics for inflammation-related diseases.

Indexed as

Adenosine TriphosphateAnimalsAntimicrobial Cationic PeptidesCell SurvivalInflammasomesInflammationInflammation MediatorsInterleukin-1betaLipopolysaccharidesMacrophage ActivationMacrophagesMaleMiceMice, Inbred C57BLMitogen-Activated Protein KinasesNF-kappa BAdenosine TriphosphateAntimicrobial Cationic PeptidesInflammasomesInflammation MediatorsInterleukin-1betaLipopolysaccharidesMitogen-Activated Protein KinasesNF-kappa BNitric OxideNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseProtein Kinase C-alphaProtein Kinase C-delta

Identifiers

PMID28750089
PMCPMC5531531
OpenAlexW2739624572

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.