Evidence map›Paper›PMID 41511062›Full record

ArticleJournal of food science2026

Avenanthramide C From Oats Possibly Exerts Anti-Inflammatory Effects in Human Umbilical Vein Endothelial Cells.

Hiroyuki Sasaki, Hirofumi Masutomi, Hajime Nagasawa, Yuma Matsumoto, Teruyuki Okuma, Tomoyuki Otsuka, Katsuyuki Ishihara, Yusuke Suzuki, Seiji Ueda

Abstract read
In one paragraph

Article in Journal of food science, 2026. 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

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

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

9 authors.

Hiroyuki SasakiResearch and Development Division, Calbee, Inc., Utsunomiya, Tochigi, Japan.ORCID https://orcid.org/0000-0002-7735-5761
Hirofumi MasutomiResearch and Development Division, Calbee, Inc., Utsunomiya, Tochigi, Japan.ORCID https://orcid.org/0009-0008-9855-1973
Hajime NagasawaDivision of Kidney Health and Aging, the Center for Integrated Kidney Research and Advance, Shimane University Faculty of Medicine, Izumo, Shimane, Japan.ORCID https://orcid.org/0000-0001-7970-8711
Yuma MatsumotoResearch and Development Division, Calbee, Inc., Utsunomiya, Tochigi, Japan.
Teruyuki OkumaDivision of Kidney Health and Aging, the Center for Integrated Kidney Research and Advance, Shimane University Faculty of Medicine, Izumo, Shimane, Japan.
Tomoyuki OtsukaDepartment of Nephrology, Juntendo University Faculty of Medicine, Tokyo, Japan.
Katsuyuki IshiharaResearch and Development Division, Calbee, Inc., Utsunomiya, Tochigi, Japan.
Yusuke SuzukiDepartment of Nephrology, Juntendo University Faculty of Medicine, Tokyo, Japan.
Seiji UedaDivision of Kidney Health and Aging, the Center for Integrated Kidney Research and Advance, Shimane University Faculty of Medicine, Izumo, Shimane, Japan.

Funding

Calbee, Inc.
6 · The paper itself

Abstract

Chronic kidney disease (CKD) is associated with inflammation and cardiovascular complications and is partly exacerbated by the uremic toxin indoxyl sulfate (IS). IS is known to activate the aryl hydrocarbon receptor (AhR) to promote vascular inflammation. On the other hand, avenanthramide C (Ave), an oat-derived polyphenol, has antioxidative and anti-inflammatory properties. Therefore, we investigated whether Ave can suppress IS-induced inflammatory responses. Analysis of serum from hemodialysis patients revealed a significant correlation between IS and interleukin-6 (IL-6) levels. In human umbilical vein endothelial cells (HUVECs), IS (≥50 µg/mL) increased IL-6 secretion, while Ave (≥10 µM) suppressed this effect. Docking simulations and in vitro experiments suggested that Ave may interact with AhR and suppress IS-induced expression of AhR target genes, including that of cytochrome P450 family 1 subfamily A member 1. High-performance liquid chromatography verified the uptake of Ave by human umbilical vein endothelial cells. Additionally, the anti-inflammatory effects of Ave were independent of the adrenergic α1 receptor, adenosine monophosphate-activated protein kinase pathways, and protein kinase B pathways. Ave suppresses IS-induced inflammation, thereby reducing IL-6 secretion in HUVECs. These findings suggest the potential of Ave as a dietary intervention for mitigating vascular inflammation in patients with CKD.

Indexed as

Anti-Inflammatory AgentsAvenaHuman Umbilical Vein Endothelial Cellsortho-AminobenzoatesCytochrome P-450 CYP1A1HumansIndicanInterleukin-6Receptors, Aryl HydrocarbonAnti-Inflammatory Agentsavenanthramide-2CCytochrome P-450 CYP1A1IndicanInterleukin-6ortho-AminobenzoatesReceptors, Aryl Hydrocarbonavenanthramide CHUVECsindoxyl sulfatepolyphenol

Identifiers

PMID41511062
PMCPMC12785505

What OpenQuestion holds

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Registered trials

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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.