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环境类固醇与斑马鱼(Danio rerio)有机阴离子转运多肽 1d1(Oatp1d1)的相互作用。

Interaction of environmental steroids with organic anion transporting polypeptide (Oatp1d1) in zebrafish (Danio rerio).

机构信息

School of Life Sciences, University of Applied Sciences and Arts Northwestern Switzerland, Muttenz, Switzerland.

Department of Environmental Systems Science, Institute of Biogeochemistry and Pollution Dynamics, Swiss Federal Institute of Technology (ETH Zürich), Zürich, Switzerland.

出版信息

Environ Toxicol Chem. 2018 Oct;37(10):2670-2676. doi: 10.1002/etc.4231. Epub 2018 Sep 19.

DOI:10.1002/etc.4231
PMID:30055005
Abstract

Steroid hormones in the aquatic environment may pose a risk to fish health due to their ubiquitous presence and high biological activity. At present, the uptake process and toxicokinetics of steroids in fish are poorly known, in particular the role of cell membrane transporters. We investigated the interaction of 17 endogenous and environmental steroids with the zebrafish organic anion transporting peptide (Oatp1d1) uptake transporter, which is prominently expressed in liver and kidneys. We selected steroids of different classes including androstenedione (A4), progesterone (P4), and its metabolites, as well as glucocorticoids and spironolactone, and analyzed their interaction with Oatp1d1 by competitive inhibition of the uptake of the fluorescent substrate Lucifer Yellow. The half-maximal inhibition (IC50) values derived from sigmoid inhibition curves were lowest for P4, and the order of increasing IC50 values was as follows: 17α-hydroxyprogesterone > clobetasol propionate > spironolactone > 21α-hydroxyprogesterone > fludrocortisone acetate and additional glucocorticoids. The interaction activity showed a positive correlation with the lipophilicity of the steroids. Our data show that different classes of steroids interact with Oatp1d1 with different activity (either by uptake or inhibition, or both). This is of importance, because in consequence, steroids may interfere with the transport of endogenous substrates, and thus physiological processes. Moreover, steroids may alter cellular trafficking of environmental contaminants by competitive inhibition of this transporter. Environ Toxicol Chem 2018;37:2670-2676. © 2018 SETAC.

摘要

水生环境中的类固醇激素由于其普遍存在和高生物活性,可能对鱼类健康构成威胁。目前,鱼类中类固醇的摄取过程和毒代动力学知之甚少,尤其是细胞膜转运蛋白的作用。我们研究了 17 种内源性和环境类固醇与斑马鱼有机阴离子转运肽(Oatp1d1)摄取转运蛋白的相互作用,该转运蛋白在肝脏和肾脏中表达明显。我们选择了不同类别的类固醇,包括雄烯二酮(A4)、孕酮(P4)及其代谢物,以及糖皮质激素和螺内酯,并通过荧光底物 Lucifer Yellow 摄取的竞争性抑制来分析它们与 Oatp1d1 的相互作用。从 sigmoid 抑制曲线得出的半最大抑制(IC50)值对 P4 最低,IC50 值增加的顺序如下:17α-羟孕酮>氯倍他索丙酸酯>螺内酯>21α-羟孕酮>醋酸氟氢可的松和其他糖皮质激素。相互作用活性与类固醇的亲脂性呈正相关。我们的数据表明,不同类别的类固醇与 Oatp1d1 相互作用的活性不同(通过摄取或抑制,或两者兼有)。这很重要,因为因此,类固醇可能会干扰内源性底物的运输,从而影响生理过程。此外,类固醇可能通过竞争性抑制这种转运蛋白来改变环境污染物的细胞内运输。Environ Toxicol Chem 2018;37:2670-2676. © 2018 SETAC.

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