Yoshioka Hiroki, Usuda Haruki, Fukuishi Nobuyuki, Nonogaki Tsunemasa, Onosaka Satomi
College of Pharmacy, Kinjo Gakuin University.
Biol Pharm Bull. 2016;39(6):1042-6. doi: 10.1248/bpb.b16-00078.
Carbon tetrachloride (CCl4) is commonly used as a chemical inducer of experimental liver injury. In addition, many studies showed that CCl4 can induce kidney damage. In the current study, we evaluated the protective effect of zinc (Zn) against CCl4-induced nephrotoxicity. We hypothesized that this protective effect would result from the ability of Zn to serve as an inducer of metallothionein (MT), a known endogenous scavenger of free radicals. We administered Zn (as ZnSO4) 50 mg/kg subcutaneously once daily for 3 successive days prior to a single intraperitoneal administration of CCl4 4 g/kg in male ddY mice. Our results showed that Zn pretreatment significantly decreased creatinine and blood urea nitrogen levels and reduced renal histopathological damage at 6 h post-CCl4 injection, observations consistent with enhanced antioxidative activity in the kidney. Moreover, kidney MT levels in the Zn+CCl4-treated group decreased by greater than 70% compared with levels in the Zn-alone group, implying that MT was consumed by CCl4-induced radicals. These findings suggest that prophylaxis with Zn protects mice from CCl4-induced acute nephrotoxicity, presumably by induction of MT, which in turn scavenges radicals induced by CCl4 exposure.
四氯化碳(CCl4)通常用作实验性肝损伤的化学诱导剂。此外,许多研究表明,CCl4可导致肾损伤。在本研究中,我们评估了锌(Zn)对CCl4诱导的肾毒性的保护作用。我们假设这种保护作用源于Zn作为金属硫蛋白(MT)诱导剂的能力,MT是一种已知的内源性自由基清除剂。在雄性ddY小鼠单次腹腔注射4 g/kg CCl4之前,我们连续3天每天皮下注射一次50 mg/kg的Zn(以ZnSO4形式)。我们的结果表明,Zn预处理显著降低了CCl4注射后6小时的肌酐和血尿素氮水平,并减轻了肾脏组织病理学损伤,这些观察结果与肾脏中抗氧化活性增强一致。此外,与单独使用Zn的组相比,Zn + CCl4处理组的肾脏MT水平降低了70%以上,这意味着MT被CCl4诱导的自由基消耗。这些发现表明,用Zn进行预防可保护小鼠免受CCl4诱导的急性肾毒性,大概是通过诱导MT,而MT又反过来清除CCl4暴露诱导的自由基。