Evidence map›Paper›PMID 36421317›Full record

ArticleAntibiotics (Basel, Switzerland)2022

Potent Anti-Inflammatory Effects of a Helix-to-Helix Peptide against

Hyosuk Son, Seong-Cheol Park, Young-Min Kim, Jong-Kook Lee, Soyoung Park, Taeuk Guk, A-Mi Yoon, Hye Song Lim, Mi-Kyeong Jang, Jung Ro Lee

Open access · goldAbstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

10 authors at 2 institutions in 1 country.

Hyosuk SonDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Seong-Cheol ParkDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Young-Min KimDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Jong-Kook LeeDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Soyoung ParkDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Taeuk GukDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
A-Mi YoonLMO Team, National Institute of Ecology (NIE), Seocheon 33657, Republic of Korea.
Hye Song LimLMO Team, National Institute of Ecology (NIE), Seocheon 33657, Republic of Korea.
Mi-Kyeong JangDepartment of Chemical Engineering, Sunchon National University, Suncheon 57922, Republic of Korea.
Jung Ro LeeLMO Team, National Institute of Ecology (NIE), Seocheon 33657, Republic of Korea.ORCID 0000-0002-9596-3330
Sunchon National University · KRNational Institute of Ecology · KR

Funding

Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology NRF-2016R1D1A3A03918533National Institute of Ecology (NIE), funded by the Ministry of Environment (MOE) of Korea NIE-A-2022-07; NIE-A-2022-11
6 · The paper itself

Abstract

Although considerable scientific research data is available for sepsis and cytokine storm syndrome, there is a need to develop new treatments or drugs for sepsis management. Antimicrobial peptides (AMPs) possess anti-bacterial and anti-inflammatory activity, neutralizing toxins such as lipopolysaccharides (LPS, endotoxin). Most AMPs have been designed as a substitute for conventional antibiotics, which kill drug-resistant pathogens. The present study aimed to determine the anti-inflammatory potential of 10 designed XIW (X: lysine, arginine, or glutamic acid) α-helical peptides in macrophages and a mouse model in the presence of LPS. Among them, WIKE-14, a peptide with a helix-to-helix structure, having the 12th amino acid substituted with glutamic acid, suppressed pro-inflammatory cytokines in RAW 264.7 macrophages. This reaction was mediated by the inhibition of the binding between LPS and macrophages. In addition, the WIKE-14 peptide exhibited a potent anti-inflammatory activity in mice ears and lungs inflamed using LPS. Thus, our results may provide useful insights for the development of anti-sepsis agents via the sequence and structure information of the WIKE-14 peptide.

Indexed as

anti-inflammatory activityantimicrobial peptidecytokineslipopolysaccharideseptic shock

Identifiers

PMID36421317
PMCPMC9686674
OpenAlexW4309705777

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.