Suppr超能文献

拟除虫菊酯类杀虫剂丙烯菊酯和胺菊酯对人类药物转运体活性的抑制作用。

Inhibition of Human Drug Transporter Activities by the Pyrethroid Pesticides Allethrin and Tetramethrin.

作者信息

Chedik Lisa, Bruyere Arnaud, Le Vee Marc, Stieger Bruno, Denizot Claire, Parmentier Yannick, Potin Sophie, Fardel Olivier

机构信息

Institut de Recherches en Santé, Environnement et Travail (IRSET), UMR INSERM U1085, Faculté de Pharmacie, 2 Avenue du Pr Léon Bernard, Rennes, France.

Pôle Pharmacie, Centre Hospitalier Universitaire, 2 rue Henri Le Guilloux, Rennes, France.

出版信息

PLoS One. 2017 Jan 18;12(1):e0169480. doi: 10.1371/journal.pone.0169480. eCollection 2017.

Abstract

Pyrethroids are widely-used chemical insecticides, to which humans are commonly exposed, and known to alter functional expression of drug metabolizing enzymes. Limited data have additionally suggested that drug transporters, that constitute key-actors of the drug detoxification system, may also be targeted by pyrethroids. The present study was therefore designed to analyze the potential regulatory effects of these pesticides towards activities of main ATP-binding cassette (ABC) and solute carrier (SLC) drug transporters, using transporter-overexpressing cells. The pyrethroids allethrin and tetramethrin were found to inhibit various ABC and SLC drug transporters, including multidrug resistance-associated protein (MRP) 2, breast cancer resistance protein (BCRP), organic anion transporter polypeptide (OATP) 1B1, organic anion transporter (OAT) 3, multidrug and toxin extrusion transporter (MATE) 1, organic cation transporter (OCT) 1 and OCT2, with IC50 values however ranging from 2.6 μM (OCT1 inhibition by allethrin) to 77.6 μM (OAT3 inhibition by tetramethrin) and thus much higher than pyrethroid concentrations (in the nM range) reached in environmentally pyrethroid-exposed humans. By contrast, allethrin and tetramethrin cis-stimulated OATP2B1 activity and failed to alter activities of OATP1B3, OAT1 and MATE2-K, whereas P-glycoprotein activity was additionally moderately inhibited. Twelve other pyrethoids used at 100 μM did not block activities of the various investigated transporters, or only moderately inhibited some of them (inhibition by less than 50%). In silico analysis of structure-activity relationships next revealed that molecular parameters, including molecular weight and lipophilicity, are associated with transporter inhibition by allethrin/tetramethrin and successfully predicted transporter inhibition by the pyrethroids imiprothrin and prallethrin. Taken together, these data fully demonstrated that two pyrethoids, i.e., allethrin and tetramethrin, can act as regulators of the activity of various ABC and SLC drug transporters, but only when used at high and non-relevant concentrations, making unlikely any contribution of these transporter activity alterations to pyrethroid toxicity in environmentally exposed humans.

摘要

拟除虫菊酯是广泛使用的化学杀虫剂,人类普遍会接触到这类物质,并且已知其会改变药物代谢酶的功能表达。另外,有限的数据表明,作为药物解毒系统关键角色的药物转运蛋白也可能是拟除虫菊酯的作用靶点。因此,本研究旨在利用过表达转运蛋白的细胞,分析这些杀虫剂对主要ATP结合盒(ABC)和溶质载体(SLC)药物转运蛋白活性的潜在调节作用。研究发现,拟除虫菊酯烯丙菊酯和胺菊酯可抑制多种ABC和SLC药物转运蛋白,包括多药耐药相关蛋白(MRP)2、乳腺癌耐药蛋白(BCRP)、有机阴离子转运多肽(OATP)1B1、有机阴离子转运体(OAT)3、多药和毒素外排转运体(MATE)1、有机阳离子转运体(OCT)1和OCT2,然而其半数抑制浓度(IC50)值范围为2.6 μM(烯丙菊酯对OCT1的抑制)至77.6 μM(胺菊酯对OAT3的抑制),因此远高于环境中接触拟除虫菊酯的人类体内所达到的拟除虫菊酯浓度(纳摩尔范围)。相比之下,烯丙菊酯和胺菊酯顺式刺激了OATP2B1的活性,且未改变OATP1B3、OAT1和MATE2-K的活性,而P-糖蛋白的活性也受到了一定程度的抑制。另外12种浓度为100 μM的拟除虫菊酯并未阻断各种被研究转运蛋白的活性,或仅对其中一些转运蛋白有中度抑制作用(抑制率低于50%)。随后对构效关系的计算机模拟分析表明,包括分子量和亲脂性在内的分子参数与烯丙菊酯/胺菊酯对转运蛋白的抑制作用相关,并成功预测了炔咪菊酯和丙炔菊酯对转运蛋白的抑制作用。综上所述,这些数据充分证明,两种拟除虫菊酯,即烯丙菊酯和胺菊酯,可作为多种ABC和SLC药物转运蛋白活性的调节剂,但只有在高浓度且不相关的情况下才会起作用,因此这些转运蛋白活性的改变不太可能对环境中接触拟除虫菊酯的人类产生拟除虫菊酯毒性作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验