Evidence map›Paper›PMID 35295338›Full record

ArticleFrontiers in pharmacology2022

Potent Inhibition of Human Cytochrome P450 3A4 by Biflavone Components from Ginkgo Biloba and Selaginella Tamariscina.

Bo Wang, Chao Shi, Lei Feng, Wei Pan, Xiang-Ge Tian, Cheng-Peng Sun, Chao Wang, Jing Ning, Xia Lv, Yan Wang and 5 more

Abstract 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Medicinal Values and Potential Risks Evaluation ofMolecules (Basel, Switzerland) · 2022
    Article
  9. 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

15 authors.

Bo WangSchool of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Chao ShiCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Lei FengCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Wei PanCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Xiang-Ge TianCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Cheng-Peng SunCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Chao WangCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Jing NingCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Xia LvCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Yan WangCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Qian-Hui YuanCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Rui-Xuan GuanCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Hou-Li ZhangCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Xiao-Chi MaCollege of Pharmacy, College of Integrative Medicine, Dalian Medical University, Dalian, China.
Tong-Hui MaSchool of Medicine & Holistic Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CYP3A4-mediated Phase I biotransformation is the rate-limiting step of elimination for many commonly used clinically agents. The modulatory effects of herbal medicines on CYP3A4 activity are one of the risk factors affecting the safe use of drug and herbal medicine. In the present study, the inhibitory effects of nearly hundred kinds of herbal medicines against CYP3A4 were evaluated based on a visual high-throughput screening method. Furthermore, biflavone components including bilobetin (7-demethylginkgetin, DGK), ginkgetin (GK), isoginkgetin (IGK), and amentoflavone (AMF) were identified as the main inhibitory components of

Indexed as

biflavonecytochrome P450 3A4herbal-drug interactioninhibition mechanismmetabolism interaction

Identifiers

PMID35295338
PMCPMC8920304

What OpenQuestion holds

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Registered trials

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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.