Evidence map›Paper›PMID 26149595›Full record

ArticleScientific reports2015

Rhein prevents endotoxin-induced acute kidney injury by inhibiting NF-κB activities.

Chen Yu, Dong Qi, Ju-Feng Sun, Peng Li, Hua-Ying Fan

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

58 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Food science & nutrition · 2025
    Article
  10. Article
  11. Aurantio-obtusin exerts an anti-inflammatory effect on acute kidney injury by inhibiting NF-κB pathway.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2024
    Article
  12. Review
  13. Article
  14. Article
  15. Macrophage angiotensin ATAmerican journal of physiology. Renal physiology · 2023
    Article
  16. Potential Medicinal Value of Rhein for Diabetic Kidney Disease.Chinese journal of integrative medicine · 2023
    Review
  17. Review
  18. Article
  19. Rhein Inhibits NF-Applied bionics and biomechanics · 2022
    Article
  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

5 authors at 4 institutions in 1 country.

Chen YuSchool of Pharmacy, Binzhou Medical University, Yantai, Shandong, China.
Dong QiDepartment of Nephrology, Yu-Huang-Ding Hospital/Qingdao University, Yantai, Shandong, China.
Ju-Feng SunSchool of Pharmacy, Binzhou Medical University, Yantai, Shandong, China.
Peng LiDepartment of Nephrology, Yu-Huang-Ding Hospital/Qingdao University, Yantai, Shandong, China.
Hua-Ying FanSchool of Pharmacy, Yantai University, Yantai, Shandong, China.
Yuhuangding Hospital · CNBinzhou Medical University · CNBinzhou University · CNYantai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to explore the effect and mechanisms of rhein on sepsis-induced acute kidney injury by injecting lipopolysaccharide (LPS) and cecal ligation and puncture (CLP) in vivo, and on LPS-induced HK-2 cells in vitro. For histopathological analysis, rhein effectively attenuated the severity of renal injury. Rhein could significantly decrease concentration of BUN and SCr and level of TNF-α and IL-1β in two different mouse models of experimental sepsis. Moreover, rhein could markedly attenuate circulating leukocyte infiltration and enhance phagocytic activity of macrophages partly impaired at 12 h after CLP. Rhein could enhance cell viability and suppresse the release of MCP-1 and IL-8 in LPS-stimulated HK-2 cells Furthermore, rhein down regulated the expression of phosphorylated NF-κB p65, IκBα and IKKβ stimulated by LPS both in vivo and in vitro. All these results suggest that rhein has protective effects on endotoxin-induced kidney injury. The underlying mechanism of rhein on anti-endotoxin kidney injury may be closely related with its anti-inflammatory and immunomodulatory properties by decreasing NF-κB activation through restraining the expression and phosphorylation of the relevant proteins in NF-κB signal pathway, hindering transcription of NF-κB p65.These evidence suggest that rhein has a potential application to treat endotoxemia-associated acute kidney injury.

Indexed as

Acute Kidney InjuryAnimalsAnthraquinonesBlood Urea NitrogenCell LineCreatineDisease Models, AnimalI-kappa B KinaseI-kappa B ProteinsImmunohistochemistryInterleukin-1betaInterleukin-8KidneyLipopolysaccharidesMacrophagesMiceAnthraquinonesCreatineI-kappa B KinaseI-kappa B ProteinsInterleukin-1betaInterleukin-8LipopolysaccharidesNF-kappa BNF-KappaB Inhibitor alphaNfkbia protein, mouserheinTranscription Factor RelATumor Necrosis Factor-alpha

Identifiers

PMID26149595
PMCPMC4493574
OpenAlexW2271362865

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.