Evidence map›Paper›PMID 31205858›Full record

ArticleTissue engineering and regenerative medicine2019

Propofol Suppresses LPS-Induced Inflammation in Amnion Cells via Inhibition of NF-κB Activation.

Ji-Young Yoon, Do-Wan Kim, Ji-Hye Ahn, Eun-Ji Choi, Yeon Ha Kim, Moonjung Jeun, Eun-Jung Kim

Open access · bronzeAbstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  12. Effect of PKC/NF-Pain research & management · 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 2 institutions in 1 country.

Ji-Young Yoon1Department of Dental Anesthesia and Pain Medicine, School of Dentistry, Pusan National University, Dental Research Institute, Geumo-ro 20, Yangsan, Gyeongnam 50612 Republic of Korea.
Do-Wan Kim1Department of Dental Anesthesia and Pain Medicine, School of Dentistry, Pusan National University, Dental Research Institute, Geumo-ro 20, Yangsan, Gyeongnam 50612 Republic of Korea.
Ji-Hye Ahn1Department of Dental Anesthesia and Pain Medicine, School of Dentistry, Pusan National University, Dental Research Institute, Geumo-ro 20, Yangsan, Gyeongnam 50612 Republic of Korea.
Eun-Ji Choi2Department of Anesthesia and Pain Medicine, School of Medicine, Pusan National University, Geumo-ro 20, Yangsan, Gyeongnam 50612 Republic of Korea.
Yeon Ha Kim3Department of Integrated Biological Science, Pusan National University, 2 Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan, 46241 Republic of Korea.
Moonjung Jeun3Department of Integrated Biological Science, Pusan National University, 2 Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan, 46241 Republic of Korea.
Eun-Jung Kim1Department of Dental Anesthesia and Pain Medicine, School of Dentistry, Pusan National University, Dental Research Institute, Geumo-ro 20, Yangsan, Gyeongnam 50612 Republic of Korea.ORCID 0000-0003-4982-9517
Pusan National University Dental Hospital · KRPusan National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Preterm labor is a leading risk factor for neonatal death and long-term impairment and linked closely with inflammation. Non-obstetric surgery is occasionally needed during pregnancy and the anesthetic drugs or surgery itself can give rise to inflammation. Here, we examined the influence of propofol pretreatment on the expression of cyclooxygenase-2 (COX-2) and prostaglandin E Methods: Human amnion-derived WISH cells were used to investigate the effect of propofol on the LPS-induced expression of inflammatory substances involved in preterm labor. For the experiment, WISH cells were pretreated with various concentrations propofol (0.01-10 μg/ml) for 1 h and then treated with LPS (1 μg/ml) for 24 h. Cytotoxicity was evaluated using MTT assay. PGE Results: Propofol showed no cytotoxicity on the WISH cells. LPS-induced PGE Conclusion: We demonstrated that propofol suppresses the expression of inflammatory substances enhanced by LPS stimulation. Furthermore, this inhibitory effect of propofol on the inflammatory substance expression is mediated by suppression of NF-κB activation.

Indexed as

AmnionCyclooxygenase 2CytokinesDinoprostoneFemaleHumansInflammationInterleukin-1betaLipopolysaccharidesNF-kappa BPeptide FragmentsPregnancyPropofolRNA, MessengerTumor Necrosis Factor-alphaCyclooxygenase 2CytokinesDinoprostoneInterleukin-1betainterleukin-1beta (163-171)LipopolysaccharidesNF-kappa BPeptide FragmentsPropofolRNA, MessengerTumor Necrosis Factor-alphaAmnionInflammationNF-κBPreterm laborPropofol

Identifiers

PMID31205858
PMCPMC6542914
OpenAlexW2947957146

What OpenQuestion holds

Textmetadata
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.