Evidence map›Paper›PMID 35721171›Full record

ArticleFrontiers in pharmacology2022

Protective Effects and Mechanisms of Yinchen Linggui Zhugan Decoction in HFD-Induced Nonalcoholic Fatty Liver Disease Rats Based on Network Pharmacology and Experimental Verification.

Hui Jiang, Tangyou Mao, Yuyue Liu, Xiang Tan, Zhongmei Sun, Yuan Cheng, Xiao Han, Yang Zhang, Jiali Wang, Lei 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. ACS omega · 2026
    Article
  2. Flavone C-Glycosides fromNutrients · 2025
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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

13 authors at 3 institutions in 1 country.

Hui JiangSchool of Graduate, Beijing University of Chinese Medicine, Beijing, China.
Tangyou MaoDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yuyue LiuDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Xiang TanShenzhen Traditional Chinese Medicine Hospital, Shenzhen, China.
Zhongmei SunDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yuan ChengDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Xiao HanDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yang ZhangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Jiali WangDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Lei ShiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yi GuoDongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Junxiang LiDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Haixiao HanDongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNShenzhen Pingle Orthopedic Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a common chronic liver disease, characterized by excessive accumulation of hepatocyte fat. However, there is no exact and effective pharmacotherapy for NAFLD. Yinchen linggui zhugan decoction (YLZD) has been widely used to treat NAFLD. Nevertheless, its pharmacological and molecular mechanisms have not been clearly elucidated. This study was carried out to investigate the active components of YLZD and explore its potential mechanisms for treating NAFLD by network pharmacology and experimental verification. The results showed that a total of 120 active components of YLZD and 365 targets were retrieved through databases, and the main active ingredients of YLZD consisted of chlorogenic acid, emodin, aloe-emodin, rhein, and geniposide. KEGG enrichment analysis revealed fundamental roles of TNF, PI3K/AKT, HIF-1α, and insulin resistance signaling pathways in the treatment of NAFLD by YLZD. Moreover, our experimental verification results showed that YLZD improved the liver pathological and cholesterol level, and reduced the expressions of TNF-α, IL-1β, IL-6, NF-κB, CCL2, and CXCL10 in NAFLD rats, which all belonged to TNF signaling pathway. The molecular docking confirmed the correlation between the four core components (chlorogenic acid, emodin, rhein, and geniposide) and key factors (TNF-α, IL-6, and NF-κB) in TNF signaling pathway. In conclusion, the present study systematically clarified the protective mechanisms of YLZD against NAFLD through targeting the TNF signaling pathway, and provided new ideas for the drug research of this disease.

Indexed as

experimental verificationmolecular dockingnetwork pharmacologynonalcoholic fatty liver diseasetraditional Chinese medicineYinchen Linggui Zhugan decoction

Identifiers

PMID35721171
PMCPMC9202027
OpenAlexW4281746199

What OpenQuestion holds

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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.