Evidence map›Paper›PMID 30680694›Full record

ArticleInflammation2019

Honokiol Attenuates Sepsis-Associated Acute Kidney Injury via the Inhibition of Oxidative Stress and Inflammation.

Shilin Xia, Hongli Lin, Han Liu, Zhidan Lu, Hui Wang, Songtao Fan, Nan Li

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

7 authors at 1 institution in 1 country.

Shilin XiaClinical Laboratory of Integrative Medicine, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.
Hongli LinDepartment of Nephrology, The First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.
Han LiuDepartment of Oral Pathology, Dalian Medical University, No.9 West Section Lvshun South Road, Dalian, 116044, Liaoning, China.
Zhidan LuIntensive Care Unit, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.
Hui WangIntensive Care Unit, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.
Songtao FanDepartment of Ophthalmology, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.
Nan LiIntensive Care Unit, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China. crystalroy2016@126.com.ORCID http://orcid.org/0000-0003-0471-6025
Dalian Medical University · CN

Funding

China Postdoctoral Science Foundation 2017M611240Liaoning Province S&T Project 20170520408National Natural Science Foundation of China 81703871
6 · The paper itself

Abstract

Acute kidney injury (AKI) is one of the most common complications of sepsis, which largely contributes to the high mortality rate of sepsis. Honokiol, a natural polyphenol from the traditional Chinese herb Magnolia officinalis, is known to possess anti-inflammatory and antioxidant activity. Here, the underlying mechanism of honokiol-induced amelioration of sepsis-associated AKI was analyzed. The expression patterns of oxidative stress moleculars and TLRs-mediated inflammation pathway were examined to identify the response of NRK-52E cells incubated with septic rats' serum to honokiol. The levels of iNOS, NO, and myeloperoxidase in NRK-52E cells were increased during sepsis, which could be reversed by honokiol. The production of GSH and SOD as in vivo antioxidant was increased after honokiol treatment. The administration of honokiol significantly inhibited TLR2/4/MyD88 signaling pathway in AKI-induced NRK-52E cells. Furthermore, ZnPPIX, the HO-1 inhibitor, weakened honokiol-mediated morphological amelioration, and the reduced level of TNF-α, IL-1β, and IL-6 in kidneys of rats subjected to CLP. Finally, Honokiol was shown to connect with the Nrf2-Keap1 dimensionally. These findings suggest that honokiol plays its protective role on sepsis-associated AKI against oxidative stress and inflammatory signals.

Indexed as

Acute Kidney InjuryAllyl CompoundsAnimalsAnti-Infective AgentsBiphenyl CompoundsCell LineInflammationLignansOxidative StressPhenolsRatsSepsisAllyl CompoundsAnti-Infective AgentsBiphenyl CompoundshonokiolLignansPhenolsAKIhonokiolinflammationoxidative stress

Identifiers

PMID30680694
OpenAlexW2912151930

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.