Nrf2 activators as potential modulators of injury in human kidney cells

被引:27
|
作者
Atilano-Roque, Amandla [1 ]
Wen, Xia [2 ]
Aleksunes, Lauren M. [2 ]
Joy, Melanie S. [1 ,3 ]
机构
[1] Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, 12850 E Montview Blvd,Mail Stop C238, Aurora, CO 80045 USA
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmacol & Toxicol, 170 Frelinghuysen Rd, Piscataway, NJ 08854 USA
[3] Univ Colorado, Sch Med, Div Renal Dis & Hypertens, Anschutz Med Campus,12605 E 16th Ave, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
Nrf2; Kidney; Nephrotoxicity; Cisplatin; Sulforaphane; Oltipraz; Oleanolic acid;
D O I
10.1016/j.toxrep.2016.01.006
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cisplatin is a chemotherapeutic agent used in the treatment of solid tumors, with clinical use often complicated by kidney toxicity. Nuclear factor (erythroid-derived-2)-like 2 (Nrf2) is a transcription factor involved in kidney protectant effects. The purpose of this study was to determine whether the Nrf2 activators oltipraz, sulforaphane, and oleanolic acid could protect human kidney cells against cisplatininduced injury and to compare the protective effects between three Nrf2 activators. Human proximal tubule cells (hPTC) and human embryonic kidney 293 cells (HEK293) were exposed to cisplatin doses in the absence and presence of Nrf2 activators. Pre- and delayed-cisplatin and Nrf2 activator exposures were also assessed. Cell viability was enhanced with Nrf2 activator exposures, with differences detected between pre- and delayed -treatments. Both sulforaphane and oltipraz increased the expression of antioxidant genes GCLC and NQ01. These findings suggest potential human kidney protective benefits of Nrf2 activators with planned exposures to cisplatin. (C) 2016 Published by Elsevier Ireland Ltd.
引用
收藏
页码:153 / 159
页数:7
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