Evidence map›Paper›PMID 29217823›Full record

ArticleExperimental & molecular medicine2017

Lysophosphatidic acid protects against acetaminophen-induced acute liver injury.

Geon Ho Bae, Sung Kyun Lee, Hyung Sik Kim, Mingyu Lee, Ha Young Lee, Yoe-Sik Bae

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. IM156, a new AMPK activator, protects against polymicrobial sepsis.Journal of cellular and molecular medicine · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Lysophospholipids in Lung Inflammatory Diseases.Advances in experimental medicine and biology · 2021
    Article
  10. Lysophosphatidic acid induces tumor necrosis factor-alpha to regulate a pro-inflammatory cytokine network in ovarian cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  11. Article
  12. The inhibitor of glycerol 3-phosphate acyltransferase FSG67 blunts liver regeneration after acetaminophen overdose by altering GSK3β and Wnt/β-catenin signaling.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2019
    Article
  13. Role of miR-223 in the pathophysiology of liver diseases.Experimental & molecular medicine · 2018
    Review
  14. Co-stimulation of LPARStem cell research & therapy · 2018
    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

6 authors at 2 institutions in 1 country.

Geon Ho BaeDepartment of Biological Sciences, Sungkyunkwan University, Suwon, Republic of Korea.
Sung Kyun LeeDepartment of Biological Sciences, Sungkyunkwan University, Suwon, Republic of Korea.
Hyung Sik KimDepartment of Biological Sciences, Sungkyunkwan University, Suwon, Republic of Korea.
Mingyu LeeDepartment of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Seoul, Republic of Korea.
Ha Young LeeDepartment of Biological Sciences, Sungkyunkwan University, Suwon, Republic of Korea.
Yoe-Sik BaeDepartment of Biological Sciences, Sungkyunkwan University, Suwon, Republic of Korea.
Sungkyunkwan University · KRSamsung (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the effect of lysophosphatidic acid (LPA) in experimental acetaminophen (APAP)-induced acute liver injury. LPA administration significantly reduced APAP-challenged acute liver injury, showing attenuated liver damage, liver cell death and aspartate aminotransferase and alanine aminotransferase levels. APAP overdose-induced mortality was also significantly decreased by LPA administration. Regarding the mechanism involved in LPA-induced protection against acute liver injury, LPA administration significantly increased the glutathione level, which was markedly decreased in APAP challenge-induced acute liver injury. LPA administration also strongly blocked the APAP challenge-elicited phosphorylation of JNK, ERK and GSK3β, which are involved in the pathogenesis of acute liver injury. Furthermore, LPA administration decreased the production of TNF-α and IL-1β in an experimental drug-induced liver injury animal model. Mouse primary hepatocytes express LPA

Indexed as

AcetaminophenAnimalsApoptosisChemical and Drug Induced Liver InjuryGene Expression RegulationHepatocytesHumansInterleukin-1betaIsoxazolesLiverLysophospholipidsMiceOxidative StressPropionatesReceptors, Lysophosphatidic AcidTumor Necrosis Factor-alpha3-(4-(4-((1-(2-chlorophenyl)ethoxy)carbonyl amino)-3-methyl-5-isoxazolyl) benzylsulfanyl) propanoic acidAcetaminophenIL1B protein, mouseInterleukin-1betaIsoxazoleslysophosphatidic acidLysophospholipidsPropionatesReceptors, Lysophosphatidic AcidTumor Necrosis Factor-alpha

Identifiers

PMID29217823
PMCPMC5750472
OpenAlexW2771783191

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.