Evidence map›Paper›PMID 36835484›Full record

ArticleInternational journal of molecular sciences2023

Untargeted Metabolomics Based Prediction of Therapeutic Potential for Apigenin and Chrysin.

Cole Cochran, Katelyn Martin, Daniel Rafferty, Jennifer Choi, Angela Leontyev, Akanksh Shetty, Sonali Kurup, Prasanth Puthanveetil

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Metabolic Responses ofPlants (Basel, Switzerland) · 2025
    Article
  3. Review
  4. 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 2 institutions in 1 country.

Cole CochranChicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Katelyn MartinChicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Daniel RaffertyChicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Jennifer ChoiChicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Angela LeontyevDepartment of Biomedical Sciences, College of Graduate Studies, Midwestern University, Downers Grove, IL 60515, USA.
Akanksh ShettyDepartment of Biomedical Sciences, College of Graduate Studies, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0001-6100-3916
Sonali KurupCollege of Pharmacy, Ferris State University, 220 Ferris Drive, Big Rapids, MI 49301, USA.
Prasanth PuthanveetilDepartment of Pharmacology, College of Graduate Studies, Midwestern University, Downers Grove, IL 60515, USA.ORCID 0000-0002-6390-3974
Midwestern University · USFerris State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prominent flavonoids apigenin and chrysin have been demonstrated to have systemic benefits. Our previous work was first to establish the impact of apigenin and chrysin on cellular transcriptome. In the current study, we have revealed the ability of apigenin and chrysin to alter the cellular metabolome based on our untargeted metabolomics. Based on our metabolomics data, both these structurally related flavonoids demonstrate diverging and converging properties. Apigenin demonstrated the potential to possess anti-inflammatory and vasorelaxant properties through the upregulation of intermediate metabolites of alpha-linolenic acid and linoleic acid pathways. Chrysin, on the other hand, exhibited abilities to inhibit protein and pyrimidine synthesis along with downregulation of gluconeogenesis pathways based on the altered metabolites detected. Chrysin-mediated metabolite changes are mostly due to its ability to modulate L-alanine metabolism and the urea cycle. On the other hand, both the flavonoids also demonstrated converging properties. Apigenin and chrysin were able to downregulate metabolites involved in cholesterol biosynthesis and uric acid synthesis, namely 7-dehydrocholesterol and xanthosine, respectively. This work will provide understanding regarding the diverse therapeutic potential of these naturally occurring flavonoids and help us in curbing an array of metabolic complications.

Indexed as

ApigeninFlavonoidsMetabolomicsUp-RegulationApigeninchrysinFlavonoidsapigeninchrysinflavonoidsmetabolomicstherapeutic prediction

Identifiers

PMID36835484
PMCPMC9967419
OpenAlexW4321374353

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.