Evidence map›Paper›PMID 42121555›Full record

ArticleFoods (Basel, Switzerland)2026

Study on the Inhibitory Effect of FOs on Advanced Glycation End Products (AGEs) Formation.

Yongmei Lyu, Haoxiang Wang, Xinying Ye, Zhihan Ge, Wanjie Mao, Zhipeng Cai, Xiaoyang Zhang, Wenlin Sun, Xiaohong Yu

Abstract read
In one paragraph

Article in Foods (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Yongmei LyuSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.ORCID 0000-0002-7285-9602
Haoxiang WangSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Xinying YeSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Zhihan GeSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Wanjie MaoSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Zhipeng CaiCollege of Food Science and Engineering, Jiangxi Agricultural University, Nanchang 330045, China.ORCID 0000-0001-8040-7609
Xiaoyang ZhangSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Wenlin SunSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.
Xiaohong YuSchool of Marine and Bioengineering, Yancheng Institute of Technology, Yancheng 224051, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study focused on the inhibitory effects of wheat bran feruloyl oligosaccharides (FOs) on the formation of AGEs in three bovine serum albumin (BSA)-based non-enzymatic glycation models, namely BSA-fructose, BSA-methylglyoxal (MGO), and BSA-glyoxal (GO). In the BSA-fructose model, FOs at 0.25 mg/mL achieved a 62% inhibition rate of fructosamine, equivalent to approximately 78% of the activity of the positive control aminoguanidine (AG), and reduced fluorescent AGEs by over 50% on day 12. Additionally, FOs suppressed the accumulation of α-dicarbonyl compounds, key intermediates in the glycation pathway. In the BSA-MGO and BSA-GO system, the decreased fluorescence intensity of tryptophan residues indicated that FOs bound to BSA, inducing conformational changes in the protein microenvironment; this binding also inhibited protein carbonyl formation and the loss of thiol groups, thereby modulating the protein glycation process. Compared with their precursors (ferulic acid, FA; xylooligosaccharides, XOS), FOs exhibited comparable or even superior inhibitory activity against specific AGE subtypes, suggesting a synergistic effect between the feruloyl and oligosaccharide moieties. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) revealed that FOs reduced the band intensity of 90 kDa AGEs in the glycation system, indicating the inhibition of protein-fructose cross-linking. Fluorescence spectroscopy confirmed that FOs dynamically quenched BSA with a single binding site, and thermodynamic calculations demonstrated that the binding was spontaneous (ΔG < 0), primarily driven by hydrogen bonds and van der Waals forces (ΔH < 0, ΔS < 0). This study systematically investigated the anti-glycation activities of FOs and their precursors. The findings demonstrate that FOs are promising natural glycation inhibitors and provide important theoretical and experimental support for related research. Furthermore, this study establish a basis for the green and high-value utilization of agricultural by-products like wheat bran.

Indexed as

advanced glycation end products (AGEs)anti-glycationferuloyl oligosaccharides (FOs)inhibitors

Identifiers

PMID42121555
PMCPMC13164026

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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.