Suppr超能文献

大鼠肾有机阴离子转运体在转运不同链长全氟羧酸中的作用。

Roles of rat renal organic anion transporters in transporting perfluorinated carboxylates with different chain lengths.

机构信息

Department of Pharmacology, Toxicology, and Therapeutics, The University of Kansas Medical Center, Kansas City, Kansas 66160, USA.

出版信息

Toxicol Sci. 2010 Feb;113(2):305-14. doi: 10.1093/toxsci/kfp275. Epub 2009 Nov 13.

Abstract

Perfluorinated carboxylates (PFCAs) are generally stable to metabolic and environmental degradation and have been found at low concentrations in environmental and biological samples. Renal clearance of PFCAs depends on chain length, species, and, in some cases, gender within species. While perfluoroheptanoate (C7) is almost completely eliminated renally in both male and female rats, renal clearance of perfluorooctanoate (C8) and perfluorononanoate (C9) is much higher in female rats. Perfluorodecanoate (C10) mainly accumulates in the liver for both genders. Therefore, we tested whether PFCAs with different chain lengths are substrates of rat renal transporters with gender-specific expression patterns. Inhibition of uptake of model substrates was measured for the basolateral organic anion transporter (Oat)1 and Oat3 and the apical Oat2, organic anion transporting polypeptide (Oatp)1a1, and Urat1 with 10microM PFCAs with chain lengths from 2 to 18 (C2-C18) carbons. Perfluorohexanoate (C6), C7, and C8 inhibited Oat1-mediated p-aminohippurate transport, with C7 being the strongest inhibitor. C8 and C9 were the strongest inhibitors for Oat3-mediated estrone-3-sulfate transport, while Oatp1a1-mediated estradiol-17beta-glucuronide uptake was inhibited by C9, C10, and perflouroundecanoate (C11), with C10 giving the strongest inhibition. No strong inhibitors were found for Oat2 or Urat1. Kinetic analysis was performed for the strongest inhibitors. Oat1 transported C7 and C8 with K(m) values of 50.5 and 43.2microM, respectively. Oat3 transported C8 and C9 with K(m) values of 65.7 and 174.5microM, respectively. Oatp1a1-mediated transport yielded K(m) values of 126.4 (C8), 20.5 (C9), and 28.5microM (C10). These results suggest that Oat1 and Oat3 are involved in renal secretion of C7-C9, while Oatp1a1 can contribute to the reabsorption of C8 through C10, with highest affinities for C9 and C10.

摘要

全氟羧酸(PFCAs)通常对代谢和环境降解具有稳定性,并且在环境和生物样本中以低浓度存在。PFCAs 的肾清除取决于链长、物种,并且在某些情况下,取决于物种内的性别。虽然全氟庚酸(C7)在雄性和雌性大鼠中几乎完全通过肾脏消除,但全氟辛酸(C8)和全氟壬酸(C9)的肾脏清除率在雌性大鼠中要高得多。对于两性,全氟癸酸(C10)主要在肝脏中积累。因此,我们测试了具有不同链长的 PFCAs 是否为具有性别特异性表达模式的大鼠肾转运体的底物。用 10μM 从 2 到 18 个(C2-C18)碳原子的链长的 PFCAs 测量了对基底外侧有机阴离子转运蛋白(Oat)1 和 Oat3 以及顶端 Oat2、有机阴离子转运多肽(Oatp)1a1 和 Urat1 的模型底物摄取的抑制作用。全氟己酸(C6)、C7 和 C8 抑制 p-氨基马尿酸转运,其中 C7 是最强的抑制剂。C8 和 C9 是雌酮-3-硫酸盐转运的 Oat3 最强抑制剂,而 Oatp1a1 介导的雌二醇-17β-葡糖苷酸摄取被 C9、C10 和全氟十一烷酸(C11)抑制,其中 C10 抑制作用最强。Oat2 或 Urat1 没有发现强抑制剂。对最强抑制剂进行了动力学分析。Oat1 分别以 50.5 和 43.2μM 的 K m 值转运 C7 和 C8。Oat3 分别以 65.7 和 174.5μM 的 K m 值转运 C8 和 C9。Oatp1a1 介导的转运产生 126.4μM(C8)、20.5μM(C9)和 28.5μM(C10)的 K m 值。这些结果表明,Oat1 和 Oat3 参与 C7-C9 的肾脏分泌,而 Oatp1a1 可以通过 C10 对 C8 的再吸收做出贡献,对 C9 和 C10 的亲和力最高。

相似文献

1
Roles of rat renal organic anion transporters in transporting perfluorinated carboxylates with different chain lengths.
Toxicol Sci. 2010 Feb;113(2):305-14. doi: 10.1093/toxsci/kfp275. Epub 2009 Nov 13.
5
Human organic anion transporter 2 is distinct from organic anion transporters 1 and 3 with respect to transport function.
Am J Physiol Renal Physiol. 2015 Nov 15;309(10):F843-51. doi: 10.1152/ajprenal.00140.2015. Epub 2015 Sep 16.
7
8
Roles of organic anion transporters in the renal excretion of perfluorooctanoic acid.
Basic Clin Pharmacol Toxicol. 2008 Jul;103(1):1-8. doi: 10.1111/j.1742-7843.2007.00155.x. Epub 2008 Jul 1.
10
Interaction of hydroxycinnamic acids and their conjugates with organic anion transporters and ATP-binding cassette transporters.
Mol Nutr Food Res. 2011 Jul;55(7):979-88. doi: 10.1002/mnfr.201000652. Epub 2011 Apr 29.

引用本文的文献

2
Perfluoroalkane Sulfonamides and Derivatives, a Different Class of PFAS: Sorption and Microbial Biotransformation Insights.
Environ Sci Technol. 2025 Jun 10;59(22):10734-10749. doi: 10.1021/acs.est.5c00906. Epub 2025 May 25.
3
Per- and polyfluoroalkyl substances (PFAS): immunotoxicity at the primary sites of exposure.
Crit Rev Toxicol. 2025;55(4):484-504. doi: 10.1080/10408444.2025.2501420. Epub 2025 May 22.
6
Bioconcentration, maternal transfer, and toxicokinetics of PFOS in a multi-generational zebrafish exposure.
Environ Toxicol Chem. 2025 Jan 1;44(1):207-219. doi: 10.1093/etojnl/vgae033.
8
Unbound Fractions of PFAS in Human and Rodent Tissues: Rat Liver a Suitable Proxy for Evaluating Emerging PFAS?
Environ Sci Technol. 2024 Aug 20;58(33):14641-14650. doi: 10.1021/acs.est.4c04050. Epub 2024 Aug 6.
9
Evaluation of 14 PFAS for permeability and organic anion transporter interactions: Implications for renal clearance in humans.
Chemosphere. 2024 Aug;361:142390. doi: 10.1016/j.chemosphere.2024.142390. Epub 2024 May 25.

本文引用的文献

3
Perfluoroalkyl chemicals and human fetal development: an epidemiologic review with clinical and toxicological perspectives.
Reprod Toxicol. 2009 Jun;27(3-4):212-230. doi: 10.1016/j.reprotox.2009.02.001. Epub 2009 Feb 20.
4
Human organic anion transporter hOAT4 is a transporter of perfluorooctanoic acid.
Basic Clin Pharmacol Toxicol. 2009 Aug;105(2):136-8. doi: 10.1111/j.1742-7843.2009.00409.x. Epub 2009 Apr 3.
5
Disposition of perfluorinated acid isomers in Sprague-Dawley rats; part 2: subchronic dose.
Environ Toxicol Chem. 2009 Mar;28(3):555-67. doi: 10.1897/08-254.1. Epub 2008 Oct 21.
6
Roles of organic anion transporters in the renal excretion of perfluorooctanoic acid.
Basic Clin Pharmacol Toxicol. 2008 Jul;103(1):1-8. doi: 10.1111/j.1742-7843.2007.00155.x. Epub 2008 Jul 1.
8
Time dependencies in perfluorooctylacids disposition in rat and monkeys: a kinetic analysis.
Toxicol Lett. 2008 Feb 28;177(1):38-47. doi: 10.1016/j.toxlet.2007.12.007. Epub 2007 Dec 27.
9
Perfluoroalkyl acids and related chemistries--toxicokinetics and modes of action.
Toxicol Sci. 2008 Mar;102(1):3-14. doi: 10.1093/toxsci/kfm270. Epub 2007 Nov 13.

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