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多药耐药蛋白1转运体可保护人和小鼠近端肾小管细胞免受百草枯诱导的毒性作用。

MDR1 transporter protects against paraquat-induced toxicity in human and mouse proximal tubule cells.

作者信息

Wen Xia, Gibson Christopher J, Yang Ill, Buckley Brian, Goedken Michael J, Richardson Jason R, Aleksunes Lauren M

机构信息

Department of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, Piscataway, New Jersey 08854.

Department of Pharmacology and Toxicology, Rutgers University Ernest Mario School of Pharmacy, Piscataway, New Jersey 08854 Joint Graduate Program in Toxicology, Rutgers University, Piscataway, New Jersey 08854.

出版信息

Toxicol Sci. 2014 Oct;141(2):475-83. doi: 10.1093/toxsci/kfu141. Epub 2014 Jul 11.

Abstract

Paraquat is a herbicide that is highly toxic to the lungs and kidneys following acute exposures. Prior studies have demonstrated that the organic cation transporter 2 and multidrug and toxin extrusion protein 1 contribute to the urinary secretion of paraquat in the kidneys. The purpose of this study was to determine whether the multidrug resistance protein 1 (MDR1/Mdr1, ABCB1, or P-glycoprotein) also participates in the removal of paraquat from the kidneys and protects against renal injury. Paraquat transport and toxicity were quantified in human renal proximal tubule epithelial cells (RPTEC) that endogenously express MDR1, HEK293 cells overexpressing MDR1, and Mdr1a/1b knockout mice. In RPTEC cells, reduction of MDR1 activity using the antagonist PSC833 or siRNA transfection increased the cellular accumulation of paraquat by 50%. Reduced efflux of paraquat corresponded with enhanced cytotoxicity in PSC833-treated cells. Likewise, stable overexpression of the human MDR1 gene in HEK293 cells reduced intracellular levels of paraquat by 50%. In vivo studies assessed the renal accumulation and subsequent nephrotoxicity of paraquat (10 or 30 mg/kg ip) in wild-type and Mdr1a/1b knockout mice. At 4 h after paraquat treatment, renal concentrations of paraquat in the kidneys of Mdr1a/1b knockout mice were 750% higher than wild-type mice. By 72 h, paraquat-treated Mdr1a/1b knockout mice had more extensive tubular degeneration and significantly greater mRNA expression of kidney injury-responsive genes, including kidney injury molecule-1, lipocalin-2, and NAD(P)H quinone oxidoreductase 1, compared with wild-type mice. In conclusion, MDR1/Mdr1 participates in the elimination of paraquat from the kidneys and protects against subsequent toxicity.

摘要

百草枯是一种除草剂,急性接触后对肺和肾脏具有高毒性。先前的研究表明,有机阳离子转运体2和多药及毒素外排蛋白1参与了百草枯在肾脏中的尿分泌。本研究的目的是确定多药耐药蛋白1(MDR1/Mdr1、ABCB1或P-糖蛋白)是否也参与肾脏中百草枯的清除并预防肾损伤。在内源性表达MDR1的人肾近端小管上皮细胞(RPTEC)、过表达MDR1的HEK293细胞以及Mdr1a/1b基因敲除小鼠中对百草枯转运和毒性进行了定量分析。在RPTEC细胞中,使用拮抗剂PSC833或siRNA转染降低MDR1活性可使百草枯的细胞内蓄积增加50%。百草枯外排减少与PSC833处理细胞中细胞毒性增强相对应。同样,在HEK293细胞中稳定过表达人MDR1基因可使百草枯的细胞内水平降低50%。体内研究评估了野生型和Mdr1a/1b基因敲除小鼠中百草枯(腹腔注射10或30mg/kg)的肾脏蓄积及随后的肾毒性。在百草枯处理后4小时,Mdr1a/1b基因敲除小鼠肾脏中百草枯的浓度比野生型小鼠高750%。到72小时时,与野生型小鼠相比,百草枯处理的Mdr1a/1b基因敲除小鼠出现更广泛的肾小管变性,肾脏损伤反应基因(包括肾损伤分子-1、脂质运载蛋白-2和NAD(P)H醌氧化还原酶1)的mRNA表达显著更高。总之,MDR1/Mdr1参与肾脏中百草枯的清除并预防随后的毒性。

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