Evidence map›Paper›PMID 24404333›Full record

ArticleBiomolecules & therapeutics2013

Emodin Isolated from Polygoni cuspidati Radix Inhibits TNF-α and IL-6 Release by Blockading NF-κB and MAP Kinase Pathways in Mast Cells Stimulated with PMA Plus A23187.

Yue Lu, Yong-Tae Jeong, Xian Li, Mi Jin Kim, Pil-Hoon Park, Seung-Lark Hwang, Jong Keun Son, Hyeun Wook Chang

Open access · bronzeAbstract read
In one paragraph

Article in Biomolecules & therapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  6. Trigonelline, An Alkaloid FromFrontiers in pharmacology · 2021
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  7. Review
  8. A Novel Peptide from Abalone (Marine drugs · 2019
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Anti-inflammatory effect of emodin on lipopolysaccharide-induced keratitis in Wistar rats.International journal of clinical and experimental medicine · 2015
    Article
  15. Article
  16. Article
  17. Review
  18. 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 1 institution in 1 country.

Yue LuSchool of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China, College of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea ; College of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Yong-Tae JeongCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Xian LiCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Mi Jin KimCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Pil-Hoon ParkCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Seung-Lark HwangCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Jong Keun SonCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Hyeun Wook ChangCollege of Pharmacy, Yeungnam University, Gyeongsan 712-749, Republic of Korea.
Yeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emodin, a naturally occurring anthraquinone derivative isolated from Polygoni cuspidati radix, has several beneficial pharmacologic effects, which include anti-cancer, anti-diabetic, and anti-inflammatory activities. In this study, the authors examined the effect of emodin on the production of proinflammatory cytokines, such as, tumor necrosis factor (TNF)-α and interleukin (IL)-6, in mouse bone marrow-derived mast cells (BMMCs) stimulated with phorbol 12-myristate 13-acetate (PMA) plus the calcium ionophore A23187. To investigate the mechanism responsible for the regulation of pro-inflammatory cytokine production by emodin, the authors assessed its effects on the activations of transcriptional factor nuclear factor-κB (NF-κB) and mitogen-activated protein kinases (MAPKs). Emodin attenuated the nuclear translocation of (NF)-κB p65 and its DNA-binding activity by reducing the phosphorylation and degradation of IκBα and the phosphorylation of IκB kinase B (IKK). Furthermore, emodin dose-dependently attenuated the phosphorylations of MAPKs, such as, extracellular signal-regulated kinase 1/2 (ERK1/2), p38 MAP kinase, and the stress-activated protein kinases (SAPK)/c-Jun-N-terminal kinase (JNK). Taken together, the findings of this study suggest that the anti-inflammatory effects of emodin on PMA plus A23187-stimulated BMMCs are mediated via the inhibition of NF-κB activation and of the MAPK pathway.

Indexed as

Bone marrow-derived mast cellsEmodinMitogen-activated protein kinaseNF-κBPMA plus A23187Pro-inflammatory cytokine

Identifiers

PMID24404333
PMCPMC3879914
OpenAlexW2022134503

What OpenQuestion holds

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Registered trials

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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.