Evidence map›Paper›PMID 40271058›Full record

ArticleFrontiers in pharmacology2025

Targeted metabolomics unravels the mechanism by phenylpropanoid-rich of the peel of

Xiaotian Cheng, Jinyan He, Yuru Yang, Yaonan He, Guangtong Chen, Bai Ling, Andong Wang

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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.

Xiaotian Cheng *School of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Jinyan He *School of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Yuru YangSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Yaonan HeSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Guangtong ChenSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Bai LingSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Andong WangSchool of Pharmacy, Nantong University, Nantong, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Diabetes is one common clinical symptoms of metabolic disorders. The peel of Purpose: The research is intended to elucidate the constituent of phenylpropanoid enriched of Methods: The constituents of YMP were systematacially identified by HPLC-Q-TOF-MS/MS and NMR. To assess the effects of varying YMP doses, diabetic mice induced by streptozotocin and a high-fat diet were divided into groups. Targeted serum metabolomics investigations were conducted using UHPLC-LTQ-Orbitrap MS. Moreover, 16S rRNA analysis was employed to elucidate the intricate mechanisms through the gut microbiota modulates lipid and glucose metabolism. Results: It demonstrated that the primary component of YMP was luteolin. At a high dosage of 160 mg/kg/day, YMP considerably reduced the values of the oral glucose tolerance test, insulin, and blood glucose ( Conclusion: This work investigated the regulating effect of YMP on the liver glycolipid metabolism for the first time, and it also showed the underlying mechanism through gut microbiota. According to these studies, YMP has a lot of potential to be used as a supplemental treatment for complex metabolic illnesses like diabetes. It offered empirical support for the use of alternative medicine in the area to treat complex problems of glucose and lipid metabolism in diabetes.

Indexed as

diabetesgut microbiomemetabolic disordersmetabonomicsZea mays L.

Identifiers

PMID40271058
PMCPMC12014729

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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.