Evidence map›Paper›PMID 32520399›Full record

ArticleBritish journal of pharmacology2020

Artesunate interacts with the vitamin D receptor to reverse sepsis-induced immunosuppression in a mouse model via enhancing autophagy.

Shenglan Shang, Jiaqi Wu, Xiaoli Li, Xin Liu, Pan Li, Chunli Zheng, Yonghua Wang, Songqing Liu, Jiang Zheng, Hong Zhou

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.4field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The Role of Vitamin D and Vitamin D Receptor in Sepsis.Current issues in molecular biology · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Vitamin D Receptor Is a Sepsis-Susceptibility Gene in Chinese Children.Medical science monitor : international medical journal of experimental and clinical research · 2021
    Article
  15. Article
  16. 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

10 authors at 4 institutions in 1 country.

Shenglan ShangMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Jiaqi WuMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Xiaoli LiMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Xin LiuMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Pan LiMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Chunli ZhengKey Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China.
Yonghua WangKey Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, Guizhou, China.
Songqing LiuDepartment of Pharmacy, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Jiang ZhengMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Hong ZhouMedical Research Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Army Medical University · CNZunyi Medical University · CNMinistry of Education of the People's Republic of China · CNSouthwest Hospital · CN

Funding

Major National Science and Technology Program of China for Innovative Drug 2017ZX09101002-002-009National Natural Science Foundation of China 81673495National Natural Science Foundation of China 81772137National Natural Science Foundation of China 81872914Special Basic Science and Cutting-edge Research Project of Chongqing cstc2015jcyjBX0049the fourth batch of "Thousand People Innovation and Entrepreneurship Talents Fund" in Guizhou Province, Shijingshan's Tutor Studio of Pharmacology GZS-2016(07)
6 · The paper itself

Abstract

background and purposeImmunosuppression is the predominant cause of mortality for sepsis because of failure to eradicate pathogens. No effective and specific drugs capable of reversing immunosuppression are clinically available. Evidences implicate the involvement of the vitamin D receptor (NR1I1) in sepsis-induced immunosuppression. The anti-malarial artesunate was investigated to determine action on sepsis-induced immunosuppression. EXPERIMENTAL APPROACH: The effect of artesunate on sepsis-induced immunosuppression was investigated in mice and human and mice cell lines. Bioinformatics predicted vitamin D receptor as a candidate target for artesunate, which was then identified using PCR and immunoblotting. Vdr, Atg16l1 and NF-κB p65 were modified to investigate artesunate 's effect on pro-inflammatory cytokines release, bacterial clearance and autophagy activities in sepsis-induced immunosuppression. KEY

resultsArtesunate significantly reduced the mortality of caecal ligation and puncture (CLP)-induced sepsis immunosuppression mice challenged with Pseudomonas aeruginosa and enhanced pro-inflammatory cytokine release and bacterial clearance to reverse sepsis-induced immunosuppression in vivo and in vitro. Mechanistically, artesunate interacted with vitamin D receptor, inhibiting its nuclear translocation, which influenced ATG16L1 transcription and subsequent autophagy activity. Artesunate inhibited the physical interaction between vitamin D receptor and NF-κB p65 in LPS-tolerant macrophages and then promoted the nuclear translocation of NF-κB p65, which activated the transcription of NF-κB p65 target genes such as pro-inflammatory cytokines. CONCLUSION AND IMPLICATIONS: Our findings provide evidence that artesunate interacted with vitamin D receptor to reverse sepsis-induced immunosuppression in an autophagy and NF-κB-dependent manner, highlighting a novel approach for sepsis treatment and drug repurposing of artesunate has a bidirectional immunomodulator.

Indexed as

ArtesunateAutophagyReceptors, CalcitriolSepsisAnimalsFemaleImmunosuppression TherapyMaleMiceMice, Inbred BALB CNF-kappa BArtesunateNF-kappa BReceptors, Calcitriol

Identifiers

PMID32520399
PMCPMC7443466
OpenAlexW3033498372

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.