Evidence map›Paper›PMID 24441569›Full record

ArticleInternational journal of molecular sciences2014

Artesunate reduces serum lipopolysaccharide in cecal ligation/puncture mice via enhanced LPS internalization by macrophages through increased mRNA expression of scavenger receptors.

Bin Li, Mengchen Yu, Xichun Pan, Chuanliang Ren, Wei Peng, Xiaoli Li, Weiwei Jiang, Jiang Zheng, Hong Zhou

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Targeting hepatic macrophages for non-alcoholic fatty liver disease therapy.Frontiers in cell and developmental biology · 2024
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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

9 authors at 1 institution in 1 country.

Bin LiDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. libin6033@sina.com.
Mengchen YuDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. agnes15@163.com.
Xichun PanDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. xichunpan@163.com.
Chuanliang RenDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. renchuanliang123@126.com.
Wei PengDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. pengwei002@126.com.
Xiaoli LiDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. plum181181@126.com.
Weiwei JiangDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. jww613@sina.com.
Jiang ZhengDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. zhengj99219@163.com.
Hong ZhouDepartment of Pharmacology, College of Pharmacy, Third Military Medical University, Chongqing 400038, China. zhouh64@163.com.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate immunity is the first line of defense in human beings against pathogen infection; monocytes/macrophages are the primary cells of the innate immune system. Recently, macrophages/monocytes have been discovered to participate in LPS clearance, and the clearance efficiency determines the magnitude of the inflammatory response and subsequent organ injury. Previously, we reported that artesunate (AS) protected sepsis mice against heat-killed E. coli challenge. Herein, we further confirmed that AS protected cecal ligation/puncture (CLP) sepsis mice. Its protection on sepsis mice was related to not only reduction of pro-inflammatory cytokines and serum LPS levels but also improvement of liver function. Based on the fact that AS did not directly bind and neutralize LPS, we hypothesized that the reduction of serum LPS level might be related to enhancement of LPS internalization and subsequent detoxification. Our results showed that AS increased FITC-LPS internalization by peritoneal macrophage and liver Kupffer cell, but enhancement of LPS internalization by AS was not related to the clathrin-dependent pathway. However, AS induced mRNA expression of important scavenger receptors (SRs); SR-A and MARCO mRNA expression was upregulated, suggesting that AS enhancement of LPS internalization and inhibition of pro-inflammatory cytokines was related to changes in mRNA expression of SRs.

Indexed as

AnimalsArtemisininsArtesunateCecumCell Culture TechniquesCells, CulturedLipopolysaccharidesMacrophagesMiceReceptors, ImmunologicRNA, MessengerScavenger Receptors, Class ASepsisArtemisininsArtesunateLipopolysaccharidesMarco protein, mouseReceptors, ImmunologicRNA, MessengerScavenger Receptors, Class A

Identifiers

PMID24441569
PMCPMC3907860
OpenAlexW2019008251

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.