Evidence map›Paper›PMID 40319366›Full record

ArticleJournal of animal science2025

Insights into rutin and quercetin biotransformations in ruminants revealed by molecular networking.

Dicky Aldian, Laila Dini Harisa, Hideki Tomita, Ke Tian, Shigeo Takashima, Atsushi Iwasawa, Masato Yayota

Abstract read
In one paragraph

Article in Journal of animal science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Dicky AldianThe United Graduate School of Agricultural Science, Gifu University, Gifu, Japan.
Laila Dini HarisaThe United Graduate School of Agricultural Science, Gifu University, Gifu, Japan.
Hideki TomitaFaculty of Applied Biological Sciences, Gifu University, Gifu, Japan.
Ke TianThe United Graduate School of Agricultural Science, Gifu University, Gifu, Japan.
Shigeo TakashimaLife Science and Research Centre, Gifu University, Gifu, Japan.
Atsushi IwasawaFaculty of Applied Biological Sciences, Gifu University, Gifu, Japan.
Masato YayotaFaculty of Applied Biological Sciences, Gifu University, Gifu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quercetin and its glycoside rutin are flavonoids that are widely used as robust antioxidants and anti-inflammatory agents for improving animal health. These compounds are metabolized into various phenolic compounds that may have stronger antioxidant activity than their original forms. However, the quercetin and rutin biotransformation pathways in ruminants have not yet been fully elucidated. To identify these pathways, we used a molecular networking approach to determine the metabolite formation of rutin and quercetin. Five Shiba crossbred wethers (51.4 ± 7.4 kg BW) were used in a balanced crossover design and were assigned to 3 different groups: the quercetin (QUE), rutin (RUT), and control (CON) groups. Rumen fluid was collected at 0, 1, 4, 6, 8, and 22 h, while blood was collected at 0, 4, and 8 h after administration and subjected to LC‒MS/MS analysis to construct the molecular network. A biomarker test was conducted to evaluate the performance of each metabolite candidate. The univariate data were analyzed via generalized linear mixed model fits in the analysis of variance (ANOVA) in R. The QUE group has a greater (P < 0.001) level of 3,4-dihydroxyphenyl acetic acid (3,4-DHPAA) concentration at 1 h than that in the RUT and CON groups but then decreased (P < 0.001) at 4 h. Then, the 4-MC concentration in the rumen of QUE group increased (P < 0.001) at 1 and 4 h post-administration. According to molecular networking, rumen microorganisms are thought to degrade rutin to produce quercetin, which is further resulted into the increase of phloroglucinol (PG) and 3,4-DHPAA. The yielded 3,4-DHPAA was suggested to be transformed into protocatechuic acid and 4-methylcatechol (4-MC). The yielded 4-MC was then transformed into 4-methylcatechol 1-sulfate (4-MC-S) through phase II metabolism via sulfation. Meanwhile, PG is metabolized to 3,5-dihydroxycyclohexan-1-one and remains undetectable in the blood. The isorhamnetin-glucuronide sulfate was a significant flavonol conjugate (P < 0.001) found in blood. In conclusion, rutin and quercetin are metabolized mainly to 4-MC-S and isorhamnetin-glucuronide sulfate in ruminants.

Indexed as

QuercetinRutinAnimalsBiotransformationCross-Over StudiesFemaleMaleRumenSheepQuercetinRutin4-methylcatecholantioxidantflavonoidmetabolism pathwaymetabolomics

Identifiers

PMID40319366
PMCPMC12201991

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.