Evidence map›Paper›PMID 35370715›Full record

ArticleFrontiers in pharmacology2022

Da-Chai-Hu-Tang Protects From Acute Intrahepatic Cholestasis by Inhibiting Hepatic Inflammation and Bile Accumulation

Shihao Xu, Xi Qiao, Peike Peng, Ziyi Zhu, Yaoting Li, Mengyuan Yu, Long Chen, Yin Cai, Jin Xu, Xinwei Shi and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Article
  8. 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

13 authors at 4 institutions in 4 countries.

Shihao XuSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Xi QiaoSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Peike PengSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Ziyi ZhuSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yaoting LiSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Mengyuan YuSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Long ChenExperimental Center for Science and Technology, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Yin CaiDepartment of Health Technology and Informatics, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China.
Jin XuSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Xinwei ShiSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Christopher G ProudLifelong Health Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Jianling XieLifelong Health Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Kaikai ShenSchool of Basic Medical Sciences, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Shanghai University of Traditional Chinese Medicine · CNFlinders University · AUHong Kong Polytechnic University · HKSouth Australian Health and Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholestasis is caused by intrahepatic retention of excessive toxic bile acids and ultimately results in hepatic failure. Da-Chai-Hu-Tang (DCHT) has been used in China to treat liver and gallbladder diseases for over 1800 years. Here, we demonstrated that DCHT treatment prevented acute intrahepatic cholestasis with liver injury in response to α-naphthylisothiocyanate (ANIT) not to bile duct ligation (BDL) induced-extrahepatic cholestasis. ANIT (80 mg/kg) increased serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), direct bilirubin (DBiL), total bilirubin (TBiL), and total bile acids (TBA) which was attenuated by DCHT treatment in a dose-dependent manner. DCHT treatment at high dose of 1.875 g/kg restored bile acid homeostasis, as evidenced by the recovery of the transcription of genes implicated in bile acid biosynthesis, uptake and efflux. DCHT treatment (1.875 g/kg) reversed ANIT-evoked disordered glutathione homeostasis (as determined by GSH/GSSG ratio) and increased in the mRNA levels for

Indexed as

bile acid homeostasisDa-Chai-Hu-Tangintrahepatic cholestasisliver injuryperoxisome proliferator-activated receptor alpha

Identifiers

PMID35370715
PMCPMC8965327
OpenAlexW4220717246

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.