Evidence map›Paper›PMID 38566171›Full record

ArticleHereditas2024

Huanglian-Hongqu herb pair improves nonalcoholic fatty liver disease via NF-κB/NLRP3 pathway in mice: network pharmacology, molecular docking and experimental validation.

Zheng Wang, Hairong Qiu, Yang Yang, Yueyu Zhang, Taiguo Mou, Xiaobo Zhang, Yong Zhang

Open access · goldAbstract read
In one paragraph

Article in Hereditas, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

7 authors at 4 institutions in 1 country.

Zheng Wang *College of Traditional Chinese Medicine and Health Service, Shanxi Datong University, Datong, China.
Hairong Qiu *Department of Chinese Medicine, Medical School, Hubei Minzu University, Enshi, China.
Yang YangInstitute of Traditional Chinese Medicine, Sichuan Academy of Chinese Medicine Sciences, Chengdu, China.
Yueyu ZhangCollege of Public health, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Taiguo MouCollege of Public health, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Xiaobo ZhangSchool of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China. zhangxiaobo@stu.cdutcm.edu.cn.ORCID http://orcid.org/0000-0002-9916-3832
Yong ZhangSchool of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China. 18692213920@163.com.
Chengdu University of Traditional Chinese Medicine · CNMinzu University of China · CNShanxi Datong University · CNSichuan Academy of Traditional Chinese Medicine · CN

Funding

Chengdu University of Traditional Chinese Medicine BSH2021016National Natural Science Foundation of China 82305085Shanxi Datong University 22ZDYF0905
6 · The paper itself

Abstract

The Huanglian-Hongqu herb pair (HH) is a carefully crafted traditional Chinese herbal compound designed to address disorders related to glucose and lipid metabolism. Its primary application lies in treating hyperlipidemia and fatty liver conditions. This study explored the potential mechanism of HH in treating non-alcoholic fatty liver disease (NAFLD) through network pharmacology, molecular docking, and in vivo animal experiments. Ultrahigh performanceliquid chromatography-quadrupole/orbitrapmass spectrometry (UPLC-Q-TOF-MS) was employed to identify the chemical composition of HH. Network pharmacology was used to analyze the related signaling pathways affected by HH. Subsequently, the prediction was verified by animal experiment. Finally, we identified 29 components within HH. Network pharmacology unveiled interactions between HH and 153 NAFLD-related targets, highlighting HH's potential to alleviate NAFLD through NF-κB signaling pathway. Molecular docking analyses illuminated the binding interactions between HH components and key regulatory proteins, including NF-κB, NLRP3, ASC, and Caspase-1. In vivo experiments demonstrated that HH alleviated NAFLD by reducing serum and liver lipid levels, improving liver function, and lowering inflammatory cytokine levels in the serum. Moreover, HH administration downregulated mRNA and protein levels of the NF-κB/NLRP3 pathway. In conclusion, our findings demonstrated that HH has potential therapeutic benefits in ameliorating NAFLD by targeting the NF-κB/NLRP3 pathway, facilitating the broader application of HH in the field of NAFLD.

Indexed as

Drugs, Chinese HerbalNF-kappa BNon-alcoholic Fatty Liver DiseaseAnimalsMiceMolecular Docking SimulationNetwork PharmacologyNLR Family, Pyrin Domain-Containing 3 ProteinDrugs, Chinese HerbalhuanglianNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinHuanglian-Hongqu herb pairMolecular dockingNetwork pharmacologyNF-κB/NLRP3 pathwayNonalcoholic fatty liver disease

Identifiers

PMID38566171
PMCPMC10988798
OpenAlexW4393870171

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.