Evidence map›Paper›PMID 28680097›Full record

ArticleScientific reports2017

Attenuation of Innate Immunity by Andrographolide Derivatives Through NF-κB Signaling Pathway.

Xin Nie, Shao-Ru Chen, Kun Wang, Yuran Peng, Yi-Tao Wang, Decai Wang, Ying Wang, Guo-Chun Zhou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.9field-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

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Journal of traditional and complementary medicine · 2024
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. 2-O-β-d-glucopyranosyl-Redox biology · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Andrographolide AlleviatesIranian journal of pharmaceutical research : IJPR
    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 2 institutions in 2 countries.

Xin NieSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211816, China.
Shao-Ru ChenState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China.
Kun WangSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211816, China.
Yuran PengSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211816, China.
Yi-Tao WangState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China.
Decai WangSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211816, China.
Ying WangState Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China. emilyywang@umac.mo.
Guo-Chun ZhouSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211816, China. gczhou@njtech.edu.cn.ORCID 0000-0003-3145-223X
Nanjing Tech University · CNUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Andrographolide derivatives or analogs exhibit potent anti-inflammatory effects in several disease models through NF-κB activity. In this study, we synthesized different andrographolide derivatives and investigated their effects on the toll-like receptor (TLR)-induced production of pro-inflammatory cytokines. Among these compounds, 3b, 5a, and 5b inhibited both TNF-α/NF-κB and TLR4/NF-κB signaling pathways. Treatment with compounds 3b, 5a, and 5b and their structural analogs, 3a and 6b, suppressed the expression of pro-inflammatory cytokines upon the activation of TLR3 and TLR4 ligands. Compounds 3b and 5a, but not 3a, 5b, or 6b, inhibited the nuclear translocation of the NF-κB p65 subunit. Treatment with compounds 3b, 5a, 3a, 5b, and 6b attenuated the phosphorylation of p65 and IκBα. Compounds 6b suppressed the expression of the NF-κB p65 subunit. However, these compounds, except for 5b, did not affect the TLR9-induced NF-κB-independent production of the pro-inflammatory cytokines, TNF-α, and IFN-β. Compound 3b potentially protected mice from LPS-induced acute pulmonary inflammation through the inhibition of p65 phosphorylation and the decrease of serum pro-inflammatory cytokines and chemokine. Our study revealed a functional structure-activity relationship between andrographolide derivatives and innate immunity. We identified compound 3b as a potent immune suppressive agent with the potential to protect acute pulmonary infection.

Indexed as

AnimalsCell LineDisease Models, AnimalDiterpenesFemaleHeLa CellsHumansImmunity, InnateLipopolysaccharidesMiceMolecular StructureNF-kappa BPhosphorylationPneumoniaSignal TransductionStructure-Activity RelationshipandrographolideDiterpenesLipopolysaccharidesNF-kappa B

Identifiers

PMID28680097
PMCPMC5498490
OpenAlexW2729933066

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.