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Interaction of soy isoflavones and their main metabolites with hOATP2B1 transporter

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A Correction to this article was published on 28 July 2018

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Abstract

Membrane organic anion-transporting polypeptides (OATPs) are responsible for the drug transmembrane transport within the human body. The function of OATP2B1 transporter can be inhibited by various natural compounds. Despite increased research interest in soya as a part of human diet, the effect of its active components to interact with hOATP2B1 has not been elucidated in a complex extent. This in vitro study examined the inhibitory effect of main soy isoflavones (daidzin, daidzein, genistin, genistein, glycitin, glycitein, biochanin A, formononetin) and their metabolites formed in vivo (S-equol, O-desmethylangolensin) towards human OATP2B1 transporter. MDCKII cells overexpressing hOATP2B1 were employed to determine quantitative inhibitory parameters of the tested compounds and to analyze mechanism/s of the inhibitory interaction. The study showed that aglycones of soy isoflavones and the main biologically active metabolite S-equol were able to significantly inhibit hOATP2B1-mediated transport. The Ki values for most of aglycones range from 1 to 20 μM. In contrast, glucosides did not exhibit significant inhibitory effect. The kinetic analysis did not indicate a uniform type of inhibition towards the hOATP2B1 although predominant mechanism of inhibition seemed to be competitive. These findings may suggest that tested soy isoflavones and their metabolites might affect transport of xenobiotics including drugs across tissue barriers via hOATP2B1.

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Change history

  • 28 July 2018

    The published online version contains mistake in the caption of Figures 3, 4 and 5 for in front of the figure legends designations “a–g”, “a–e”, and “a–b” have been provided. Such data should be deleted.

Abbreviations

BCA:

Bicinchoninic acid

BSA:

Bovine serum albumin

DMSO:

Dimethyl sulfoxide

E3S:

Estrone 3-sulfate

MDCKII:

Madin-Darby canine kidney II

OATP:

Organic anion transporting polypeptide

ODMA:

O-Desmethylangolensin

SLC:

Solute carrier

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Funding

This work was supported by the Grant Agency of Charles University (grant 30216/C/2016), Charles University (grants SVV 260 414 and PROGRES Q42), and the Czech Science Foundation (grant P303/12/G163).

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Authors and Affiliations

Authors

Contributions

LN, LA, and PH conducted the experiments. FT, PM, and PP participated in research design. LN and FT analyzed the experimental data. FT, LN, PM, and PP wrote and corrected the manuscript. All authors read and approved the manuscript.

Corresponding author

Correspondence to František Trejtnar.

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No animals or human subjects were involved in the study.

Conflict of interest

The authors declare that they have no conflicts of interest.

Additional information

The original version of this article was revised: The published online version contains mistake in the caption of Figures 3, 4 and 5 for in front of the figure legends designations “a–g”, “a–e”, and “a–b” have been provided. Such data should be deleted.

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Navrátilová, L., Applová, L., Horký, P. et al. Interaction of soy isoflavones and their main metabolites with hOATP2B1 transporter. Naunyn-Schmiedeberg's Arch Pharmacol 391, 1063–1071 (2018). https://doi.org/10.1007/s00210-018-1528-y

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  • DOI: https://doi.org/10.1007/s00210-018-1528-y

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