Evidence map›Paper›PMID 30610157›Full record

ArticleBioscience reports2019

Shenqi Fuzheng Injection impairs bile duct ligation-induced cholestatic liver injury

Fei Cao, Peng Liu, Xianbin Zhang, Yanfen Hu, Xin Dong, Haidong Bao, Lingkai Kong, Lei Wang, Peng Gong

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Exploring the Potential Mechanisms of Action ofCombinatorial chemistry & high throughput screening · 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 3 institutions in 2 countries.

Fei CaoDepartment of General Surgery, The Shenzhen University General Hospital; Carson International Cancer Research Centre, Shenzhen University School of Medicine, Shenzhen 518055, China caofeinmg@163.com gongpengdalian@163.com.ORCID 0000-0003-4617-405X
Peng LiuDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian 116011, China.
Xianbin ZhangInstitute for Experimental Surgery, Rostock University Medical Center, Rostock 18057, Germany.
Yanfen HuInstitute of Cancer Stem Cell, Dalian Medical University Cancer Center, Dalian 116044, China.
Xin DongDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian 116011, China.
Haidong BaoDepartment of Digestive Endoscopy, The First Affiliated Hospital of Dalian Medical University, Dalian 116011, China.
Lingkai KongInstitute of Cancer Stem Cell, Dalian Medical University Cancer Center, Dalian 116044, China.
Lei WangDepartment of Hepatobiliary Surgery, Dalian Municipal Central Hospital Affiliated of Dalian Medical University, Dalian 116033, China.
Peng GongDepartment of General Surgery, The Shenzhen University General Hospital; Carson International Cancer Research Centre, Shenzhen University School of Medicine, Shenzhen 518055, China.
Dalian Medical University · CNShenzhen University · CNUniversity of Rostock · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimThe aim of the present study sought to determine the protective function of Shenqi Fuzheng Injection (SFI) in cholestatic liver injury.

methodsCholestatic liver injury was induced in a 7-day bile duct-ligated (BDL) rat model. Rats were divided into three groups that were comprised of: (1) Sham; (2) BDL model; and (3) SFI treatment. The sham and BDL groups were treated with an appropriate volume of 0.9% sodium chloride as the vehicle, and the SFI group was administered SFI at a dose of 20 ml/kg/day, via tail vein injection.

resultsSFI significantly (all at

conclusionsThese data demonstrated that SFI attenuated both inflammation and oxidative stress, and disrupted cholestatic liver injury. The involved mechanism was dependent, at least in part, on regulating PPAR-γ, COX-2, and NF-κBp65 expression.

Indexed as

AnimalsBile DuctsCholestasisDisease Models, AnimalDrugs, Chinese HerbalGene Expression RegulationHumansLigationLipid PeroxidationLiverLiver DiseasesOxidative StressPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaRatsTranscription Factor RelADrugs, Chinese HerbalPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, ratRela protein, ratshenqi fuzhengTranscription Factor RelAbile duct ligationcholestatic liver injuryinflammationoxidative stressShenqi Fuzheng Injection

Identifiers

PMID30610157
PMCPMC6350043
OpenAlexW2907766805

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.