Evidence map›Paper›PMID 23641818›Full record

ArticleBMC gastroenterology2013

Anti-inflammatory and anti-oxidative effects of corilagin in a rat model of acute cholestasis.

Feng Jin, Du Cheng, Jun-Yan Tao, Shu-Ling Zhang, Ran Pang, Yuan-Jin Guo, Pian Ye, Ji-Hua Dong, Lei Zhao

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
9.2field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 87 citations in OpenAlex.

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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 6 institutions in 2 countries.

Feng JinDepartment of Neurosurgery, Neuro-oncology Laboratory, Affiliated Hospitalof Jining Medical College, Jining, Shandong 272029, PR China.
Du Cheng
Jun-Yan Tao
Shu-Ling Zhang
Ran Pang
Yuan-Jin Guo
Pian Ye
Ji-Hua Dong
Lei Zhao
Huazhong University of Science and Technology · CNAffiliated Hospital of Jining Medical University · CNCentral South University · CNUnion Hospital · CNUnion Hospital · CNUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNowadays, treatments for cholestasis remain largely nonspecific and often ineffective. Recent studies showed that inflammatory injuries and oxidative stress occur in the liver with cholestasis. In this study, we would use corilagin to treat the animal model of acute cholestasis in order to define the activity to interfere with inflammation-related and oxidative stress pathway in cholestatic pathogenesis.

methodsRats were administrated with alpha-naphthylisothiocyanate to establish model of cholestasis and divided into corilagin, ursodeoxycholic acid, dexamethasone, model and normal groups with treatment of related agent. At 24h, 48h and 72h time points after administration, living condition, serum markers of liver damage, pathological changes of hepatic tissue, nuclear factor (NF)-kappaB, myeloperoxidase (MPO), malondialdehyde (MDA), superoxide dismutase (SOD) and nitric oxide (NO) were examined and observed.

resultsCompared to model group, corilagin had remarkable effect on living condition, pathological manifestation of liver tissue, total bilirubin, direct bilirubin, (P<0.01), but no effect on alanine aminotransferase (ALT) and aspartate aminotransferase (AST). With corilagin intervention, levels of MPO, MDA and translocation of NF-κB were notably decreased, and levels of SOD and NO were markedly increased (P<0.05 or P<0.01).

conclusionsIt is shown that corilagin is a potential component to relieve cholestasis through inflammation-related and oxidation-related pathway.

Indexed as

Acute DiseaseAlanine TransaminaseAnalysis of VarianceAnimalsAnti-Inflammatory AgentsAspartate AminotransferasesBilirubinCholagogues and CholereticsCholestasisDexamethasoneDisease Models, AnimalGlucosidesHydrolyzable TanninsLiverMaleMalondialdehydeAlanine TransaminaseAnti-Inflammatory AgentsAspartate AminotransferasesBilirubinCholagogues and CholereticscorilaginDexamethasoneGlucosidesHydrolyzable TanninsMalondialdehydeNF-kappa BNitric OxidePeroxidaseSuperoxide DismutaseUrsodeoxycholic Acid

Identifiers

PMID23641818
PMCPMC3655894
OpenAlexW2145694499

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.