Hazelhoff María H, Bulacio Romina P, Torres Adriana M
Pharmacology, Faculty of Biochemist and Pharmaceutical Sciences, National University of Rosario, CONICET, Rosario 2000, Argentina.
Int J Mol Sci. 2012;13(8):10523-10536. doi: 10.3390/ijms130810523. Epub 2012 Aug 22.
The aim of this study was to determine if there are sex-related differences in the acute kidney injury induced by HgCl(2) since female rats express lower levels of renal Oat1 and Oat3 (transporters involved in renal uptake of mercury) as compared with males. Control males and females and Hg-treated male and female Wistar rats were employed. Animals were treated with HgCl(2) (4 mg/kg body weight (b.w.), intraperitoneal (i.p.)) 18 h before the experiments. HgCl(2) induced renal impairment both in male and female rats. However, female rats showed a lower renal impairment than male rats. The observed increase in kidney weight/body weight ratio seen in male and female rats following HgCl(2) treatment was less in the female rats. Urine volume and creatinine clearance decreased and Oat5 urinary excretion increased in both males and females, but to a lesser degree in the latter. Urinary alkaline phosphatase (AP) activity and histological parameters were modified in male but not in female rats after HgCl(2) administration. These results indicate that the lower Oat1 and Oat3 expression in the kidney of females restricts Hg uptake into renal cells protecting them from this metal toxicity. These gender differences in renal injury induced by mercury are striking and also indicate that Oat1 and Oat3 are among the main transporters responsible for HgCl(2)-induced renal injury.
本研究的目的是确定氯化汞诱导的急性肾损伤是否存在性别差异,因为与雄性大鼠相比,雌性大鼠肾脏中Oat1和Oat3(参与汞肾脏摄取的转运蛋白)的表达水平较低。使用了对照雄性和雌性大鼠以及经汞处理的雄性和雌性Wistar大鼠。在实验前18小时,用氯化汞(4mg/kg体重,腹腔注射)对动物进行处理。氯化汞在雄性和雌性大鼠中均诱导了肾脏损伤。然而,雌性大鼠的肾脏损伤程度低于雄性大鼠。在氯化汞处理后,雄性和雌性大鼠肾脏重量/体重比的增加在雌性大鼠中较少。雄性和雌性大鼠的尿量和肌酐清除率均降低,Oat5尿排泄增加,但雌性大鼠的变化程度较小。给予氯化汞后,雄性大鼠的尿碱性磷酸酶(AP)活性和组织学参数发生改变,而雌性大鼠未发生改变。这些结果表明,雌性大鼠肾脏中较低的Oat1和Oat3表达限制了汞摄取到肾细胞中,从而保护它们免受这种金属毒性的影响。汞诱导的肾脏损伤中的这些性别差异很显著,也表明Oat1和Oat3是导致氯化汞诱导的肾脏损伤的主要转运蛋白。