Nakagawa Hatsuki, Hirata Taku, Terada Tomohiro, Jutabha Promsuk, Miura Daisaku, Harada Kouji H, Inoue Kayoko, Anzai Naohiko, Endou Hitoshi, Inui Ken-Ichi, Kanai Yoshikatsu, Koizumi Akio
Department of Health and Environmental Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Basic Clin Pharmacol Toxicol. 2008 Jul;103(1):1-8. doi: 10.1111/j.1742-7843.2007.00155.x. Epub 2008 Jul 1.
Perfluorooctanoic acid, an environmental contaminant, is found in both wild animals and human beings. There are large species and sex differences in the renal excretion of perfluorooctanoic acid. In the present study, we aimed to characterize organic anion transporters 1-3 (OAT1-3) in human beings and rats to investigate whether the species differences in the elimination kinetics of perfluorooctanoic acid from the kidneys can be attributed to differences in the affinities of these transporters for perfluorooctanoic acid. We used human (h) and rat (r) OAT transient expression cell systems and measured the [(14)C] perfluorooctanoic acid transport activities. Both human and rat OAT1 and OAT3 mediated perfluorooctanoic acid transport to similar degrees. Specifically, the kinetic parameters, K(m), were 48.0 +/- 6.4 microM for h OAT1; 51.0 +/- 12.0 microM for rOAT1; 49.1 +/- 21.4 microM for hOAT3 and 80.2 +/- 17.8 microM for rOAT3, respectively. These data indicate that both human and rat OAT1 and OAT3 have high affinities for perfluorooctanoic acid and that the species differences in its renal elimination are not attributable to affinity differences in these OATs between human beings and rats. In contrast, neither hOAT2 nor rOAT2 transported perfluorooctanoic acid. In conclusion, OAT1 and OAT3 mediated perfluorooctanoic acid transport in vitro, suggesting that these transporters also transport perfluorooctanoic acid through the basolateral membrane of proximal tubular cells in vivo in both human beings and rats. Neither human nor rat OAT2 mediated perfluorooctanoic acid transport. Collectively, the difference between the perfluorooctanoic acid half-lives in human beings and rats is not likely to be attributable to differences in the affinities of these transporters for perfluorooctanoic acid.
全氟辛酸是一种环境污染物,在野生动物和人类体内均有发现。全氟辛酸的肾脏排泄存在较大的物种和性别差异。在本研究中,我们旨在对人类和大鼠的有机阴离子转运体1 - 3(OAT1 - 3)进行表征,以研究全氟辛酸从肾脏消除动力学的物种差异是否可归因于这些转运体对全氟辛酸亲和力的差异。我们使用人类(h)和大鼠(r)的OAT瞬时表达细胞系统,并测量了[¹⁴C]全氟辛酸的转运活性。人类和大鼠的OAT1及OAT3介导全氟辛酸转运的程度相似。具体而言,动力学参数K(m),hOAT1为48.0±6.4微摩尔;rOAT1为51.0±12.0微摩尔;hOAT3为49.1±21.4微摩尔;rOAT3为80.2±17.8微摩尔。这些数据表明,人类和大鼠的OAT1及OAT3对全氟辛酸均具有高亲和力,且其肾脏消除的物种差异并非归因于人类和大鼠之间这些OATs亲和力的差异。相比之下,hOAT2和rOAT2均不转运全氟辛酸。总之,OAT1和OAT3在体外介导全氟辛酸转运,这表明这些转运体在体内也通过人类和大鼠近端肾小管细胞的基底外侧膜转运全氟辛酸。人类和大鼠的OAT2均不介导全氟辛酸转运。总体而言,人类和大鼠全氟辛酸半衰期的差异不太可能归因于这些转运体对全氟辛酸亲和力的差异。