Evidence map›Paper›PMID 38256064›Full record

ArticleInternational journal of molecular sciences2024

The Use of an Antioxidant Enables Accurate Evaluation of the Interaction of Curcumin on Organic Anion-Transporting Polypeptides 4C1 by Preventing Auto-Oxidation.

Toshihiro Sato, Ayaka Yagi, Minami Yamauchi, Masaki Kumondai, Yu Sato, Masafumi Kikuchi, Masamitsu Maekawa, Hiroaki Yamaguchi, Takaaki Abe, Nariyasu Mano

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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
–field-weighted citation impact, top 100% of its field
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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

10 authors at 3 institutions in 1 country.

Toshihiro SatoDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.ORCID 0000-0002-8807-2417
Ayaka YagiGraduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
Minami YamauchiGraduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
Masaki KumondaiDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.ORCID 0000-0002-2333-2847
Yu SatoDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.ORCID 0000-0002-8979-2408
Masafumi KikuchiDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.ORCID 0000-0003-2148-6129
Masamitsu MaekawaDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.ORCID 0000-0001-6723-0298
Hiroaki YamaguchiDepartment of Pharmacy, Yamagata University Hospital, Yamagata 990-9585, Japan.ORCID 0000-0003-3021-6120
Takaaki AbeDivision of Nephrology, Endocrinology, and Vascular Medicine, Graduate School of Medicine, Tohoku University, Sendai 980-8574, Japan.
Nariyasu ManoDepartment of Pharmaceutical Sciences, Tohoku University Hospital, Sendai 980-8574, Japan.
Tohoku University · JPTohoku University Hospital · JPYamagata University · JP

Funding

Japan Society for the Promotion of Science 20K16037Japan Society for the Promotion of Science 22K15311Mishima Kaiun Memorial Foundation Toshihiro Sato
6 · The paper itself

Abstract

Flavonoids have garnered attention because of their beneficial bioactivities. However, some flavonoids reportedly interact with drugs via transporters and may induce adverse drug reactions. This study investigated the effects of food ingredients on organic anion-transporting polypeptide (OATP) 4C1, which handles uremic toxins and some drugs, to understand the safety profile of food ingredients in renal drug excretion. Twenty-eight food ingredients, including flavonoids, were screened. We used ascorbic acid (AA) to prevent curcumin oxidative degradation in our method. Twelve compounds, including apigenin, daidzein, fisetin, genistein, isorhamnetin, kaempferol, luteolin, morin, quercetin, curcumin, resveratrol, and ellagic acid, altered OATP4C1-mediated transport. Kaempferol and curcumin strongly inhibited OATP4C1, and the

Indexed as

CurcuminFood IngredientsAnionsAntioxidantsAscorbic AcidFlavonoidsKaempferolsKineticsPeptidesAnionsAntioxidantsAscorbic AcidCurcuminFlavonoidsFood IngredientsKaempferolsPeptidesascorbic acidcurcuminflavonoidsfood–drug interactionkaempferolOATP4C1renal transporter

Identifiers

PMID38256064
PMCPMC10815578
OpenAlexW4390788615

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.