Evidence map›Paper›PMID 40167032›Full record

ArticleJournal of agricultural and food chemistry2025

Detoxification of Lipid Peroxidation Aldehyde 4-Hydroxynonenal by Hesperetin Dihydrochalcone, a Microbial Metabolite of Neohesperidin Dihydrochalcone, In Vitro and In Vivo.

Richmond Djorgbenoo, Shuwei Zhang, Yingdong Zhu, Femi Omoniyi, Shengmin Sang

Abstract read
In one paragraph

Article in Journal of agricultural and food chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Dietary supplementation with walnut (Frontiers in veterinary science · 2026
    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

5 authors.

Richmond DjorgbenooLaboratory for Functional Foods and Human Health, Center for Excellence in Post-Harvest Technologies, North Carolina Agricultural and Technical State University, North Carolina Research Campus, 500 Laureate Way, Kannapolis, North Carolina 28081, United States.
Shuwei ZhangLaboratory for Functional Foods and Human Health, Center for Excellence in Post-Harvest Technologies, North Carolina Agricultural and Technical State University, North Carolina Research Campus, 500 Laureate Way, Kannapolis, North Carolina 28081, United States.
Yingdong ZhuLaboratory for Functional Foods and Human Health, Center for Excellence in Post-Harvest Technologies, North Carolina Agricultural and Technical State University, North Carolina Research Campus, 500 Laureate Way, Kannapolis, North Carolina 28081, United States.
Femi OmoniyiLaboratory for Functional Foods and Human Health, Center for Excellence in Post-Harvest Technologies, North Carolina Agricultural and Technical State University, North Carolina Research Campus, 500 Laureate Way, Kannapolis, North Carolina 28081, United States.
Shengmin SangLaboratory for Functional Foods and Human Health, Center for Excellence in Post-Harvest Technologies, North Carolina Agricultural and Technical State University, North Carolina Research Campus, 500 Laureate Way, Kannapolis, North Carolina 28081, United States.ORCID 0000-0002-5005-3616

Funding

Biomarkers of Dietary Flavonoid Intake, Carbonyl Stress, and Metabolic RiskR01DK131753 · NIDDK · NORTH CAROLINA AGRI & TECH ST UNIV · PI Shilpa Nandana Bhupathiraju, Shengmin Sang · 2022 to 2026
$2.6M
NIDDK NIH HHS R01 DK131753
6 · The paper itself

Abstract

Neohesperidin dihydrochalcone (NHDC) is a safe and widely used sweetener from citrus hesperidin. Beyond its sweetening properties, the potential health benefits and mechanisms of NHDC remain underexplored. This study investigated whether NHDC could reduce lipid peroxidation through its microbial metabolite, hesperetin dihydrochalcone (HDC), which traps 4-hydroxynonenal (4-HNE), a reactive carbonyl species generated during lipid peroxidation. In vitro, HDC formed covalent conjugates with 4-HNE through 1,2-addition at the aldehyde site and 1,4-Michael addition at the α,β-unsaturated aldehyde, resulting in three distinct adducts that were purified and characterized by NMR spectroscopy. Mouse studies confirmed that HDC is the primary metabolite of NHDC and can trap 4-HNE in vivo, forming 4-HNE-HDC conjugates. Further research showed a dose-dependent increase in 4-HNE-HDC conjugates, particularly the mono-4-HNE HDC conjugate formed via 1,2-addition. These findings demonstrate the ability of HDC to reduce carbonyl stress by trapping 4-HNE and highlight the role of microbial metabolism in the transformation of dietary polyphenols into bioactive metabolites. The 4-HNE-scavenging ability of HDC suggests its potential in the development of dietary strategies for reducing lipid peroxidation and preventing chronic diseases associated with carbonyl stress.

Indexed as

AldehydesChalconesHesperidinLipid PeroxidationAnimalsInactivation, MetabolicMaleMice4-hydroxy-2-nonenalAldehydesChalconeshesperetinHesperidinneohesperidin dihydrochalcone4-hydroxynonenaldetoxificationhesperetin dihydrochalconelipid peroxidationmouse studyneohesperidin dihydrochalcone

Identifiers

PMID40167032
PMCPMC12020420

What OpenQuestion holds

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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.