Evidence map›Paper›PMID 27746874›Full record

ArticleIranian journal of basic medical sciences2016

Hepatoprotective effects of licochalcone B on carbon tetrachloride-induced liver toxicity in mice.

Haifeng Teng, Meng Chen, Ansheng Zou, Haili Jiang, Jichun Han, Long Sun, Chao Feng, Ju Liu

Open access · greenAbstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.8field-weighted citation impact, top 8% 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, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Licochalcone D fromInternational journal of molecular sciences · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Salvianolic acid B protects hepatocytes from HWorld journal of gastroenterology · 2017
    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 4 institutions in 1 country.

Haifeng TengWeihai Municipal Hospital, China.
Meng ChenYantai Yuhuangding Hospital of Laishan Branch, China.
Ansheng ZouYantai City Hospital for Infectious Diseases, China.
Haili JiangShuguang Hospital, Shanghai University of Traditional Chinese Medicine, China.
Jichun HanShandong Provincial Qianfoshan Hospital, China.
Long SunYishui Central Hospital, China.
Chao FengYantaishan Hospital, China.
Ju LiuShandong Provincial Qianfoshan Hospital, China.
Shandong Provincial QianFoShan Hospital · CNShanghai University of Traditional Chinese Medicine · CNWeihai Municipal Hospital · CNYantaishan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of this study was to investigate the hepatoprotective effect of licochalcone B (LCB) in a mice model of carbon tetrachloride (CCl MATERIALS AND

methodsHepatotoxicity was induced in mice by a single subcutaneous injection (SC) of CCl4. The LCB was administered orally once a day for seven days (PO) as pretreatment at three doses of 1, 5, and 25 mg/kg/day. The levels of superoxide dismutase (SOD), malondialdehyde (MDA), glutathione (GSH), glutathione disulfide (GSSG), C-reactive protein (CRP), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed by ELISA. The protein expression degrees of p38 mitogen activated protein kinases (p38) and nuclear factor-k-gene binding (NF-κB) were assayed by western blotting.

resultsCCl4-induced hepatotoxicity was manifested by an increase in the levels of ALT, AST, MDA, IL-6, CRP, and TNF-ɑ, and a decrease in the SOD level and GSH/GSSG ratio in the serum. The histopathological examination of the liver sections revealed necrosis and inflammatory reactions. Pretreatment with LCB decreased the levels of ALT, AST, MDA, GSSG, IL-6, CRP, TNF-ɑ, and the protein expression of p38 and NF-κB, increased the level of SOD and GSH, and normalized the hepatic histo-architecture.

conclusionLCB protected the liver from CCl4-induced injury. Protection may be due to inhibition of p38 and NFκB signaling, which subsequently reduced inflammation in the liver.

Indexed as

Anti-inflammatoryAntioxidantCarbon tetrachlorideHepatotoxicityLicochalcone BNF-κBP38

Identifiers

PMID27746874
PMCPMC5048128
OpenAlexW2514434055

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.