Evidence map›Paper›PMID 24682220›Full record

ArticlePloS one2014

Caffeine inhibits the activation of hepatic stellate cells induced by acetaldehyde via adenosine A2A receptor mediated by the cAMP/PKA/SRC/ERK1/2/P38 MAPK signal pathway.

He Wang, Wenjie Guan, Wanzhi Yang, Qi Wang, Han Zhao, Feng Yang, Xiongwen Lv, Jun Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Review
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  7. Review
  8. Purinergic Signaling in Non-Parenchymal Liver Cells.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Coffee, adenosine, and the liver.Purinergic signalling · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Caffeine Protects Against Retinal Inflammation.Frontiers in pharmacology · 2021
    Article
  18. Article
  19. Review
  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

8 authors at 3 institutions in 1 country.

He WangSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Wenjie GuanThe 105th Hospital of PLA, Hefei, Anhui, China.
Wanzhi YangThe First Hospital of Anqing, Anqing, Anhui, China.
Qi WangSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Han ZhaoSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Feng YangSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Xiongwen LvSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Jun LiSchool of Pharmacy, Anhui Medical University, Hefei, Anhui, China; Institute for Liver Disease of Anhui Medical University, Hefei, Anhui, China.
Anhui Medical University · CN82th Hospital of Pla · CNAnqing City Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledHepatic stellate cell (HSC) activation is an essential event during alcoholic liver fibrosis. Evidence suggests that adenosine aggravates liver fibrosis via the adenosine A2A receptor (A2AR). Caffeine, which is being widely consumed during daily life, inhibits the action of adenosine. In this study, we attempted to validate the hypothesis that caffeine influences acetaldehyde-induced HSC activation by acting on A2AR. Acetaldehyde at 50, 100, 200, and 400 μM significantly increased HSC-T6 cells proliferation, and cell proliferation reached a maximum at 48 h after exposure to 200 μM acetaldehyde. Caffeine and the A2AR antagonist ZM241385 decreased the cell viability and inhibited the expression of procollagen type I and type III in acetaldehyde-induced HSC-T6 cells. In addition, the inhibitory effect of caffeine on the expression of procollagen type I was regulated by A2AR-mediated signal pathway involving cAMP, PKA, SRC, and ERK1/2. Interestingly, caffeine's inhibitory effect on the expression of procollagen type III may depend upon the A2AR-mediated P38 MAPK-dependent pathway.

conclusionsCaffeine significantly inhibited acetaldehyde-induced HSC-T6 cells activation by distinct A2AR mediated signal pathway via inhibition of cAMP-PKA-SRC-ERK1/2 for procollagen type I and via P38 MAPK for procollagen type III.

Indexed as

AcetaldehydeCaffeineCell ProliferationCells, CulturedCyclic AMPCyclic AMP-Dependent Protein KinasesGenes, srcHepatic Stellate CellsHumansMAP Kinase Signaling Systemp38 Mitogen-Activated Protein KinasesReceptor, Adenosine A2ASignal TransductionAcetaldehydeCaffeineCyclic AMPCyclic AMP-Dependent Protein Kinasesp38 Mitogen-Activated Protein KinasesReceptor, Adenosine A2A

Identifiers

PMID24682220
PMCPMC3969328
OpenAlexW1980951436

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.