Pharmacology Department, Faculty of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
BMC Complement Altern Med. 2012 May 2;12:60. doi: 10.1186/1472-6882-12-60.
Nanoparticles are small-scale substances (<100 nm) with unique properties. Therefore, nanoparticles pose complex health risk implications. The objective of this study was to detect whether treatment with quercetin (Qur) and/or arginine (Arg) ameliorated nephrotoxicity induced by two different doses of nano zinc oxide (n-ZnO) particles.
ZnO nanoparticles were administered orally in two doses (either 600 mg or 1 g/Kg body weight/day for 5 conscutive days) to Wister albino rats. In order to detect the protective effects of the studied antioxidants against n-ZnO induced nepherotoxicity, different biochemical parameters were investigated. Moreover, histopathological examination of kidney tissue was performed.
Nano zinc oxide-induced nephrotoxicity was confirmed by the elevation in serum inflammatory markers including: tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6); and C-reactive protein (CRP). Moreover, immunoglobulin (IGg), vascular endothelium growth factor (VEGF), and nitric oxide (NO) were significantly increased in rat serum. Serum urea and creatinine levels were also significantly increased in rats intoxicated with n-ZnO particles compared with the control group. Additionally, a significant decrease in the non-enzymatic antioxidant reduced glutathione (GSH) was shown in kidney tissues and serum glucose levels were increased. These biochemical findings were supported by a histopathological examination of kidney tissues, which showed that in the animals that received a high dose of n-ZnO, numerous kidney glomeruli underwent atrophy and fragmentation. Moreover, the renal tubules showed epithelial desquamation, degeneration and necrosis. Some renal tubules showed casts in their lumina. Severe congestion was also observed in renal interstitium. These effects were dose dependent. Cotreatment of rats with Qur and/or Arg along with n-ZnO significantly improved most of the deviated tested parameters.
The data show that Qur has a beneficial effect against n-ZnO oxidative stress and related vascular complications. Also, its combination with Arg proved to be even more effective in ameliorating nano zinc oxide nephrotoxicity.
纳米粒子是一种具有独特性质的小尺度物质(<100nm)。因此,纳米粒子带来了复杂的健康风险。本研究的目的是检测槲皮素(Qur)和/或精氨酸(Arg)的治疗是否可以改善两种不同剂量纳米氧化锌(n-ZnO)颗粒引起的肾毒性。
将 ZnO 纳米粒子以两种剂量(每天 600mg 或 1g/kg 体重,连续 5 天)口服给予 Wister 白化大鼠。为了检测研究中的抗氧化剂对 n-ZnO 诱导的肾毒性的保护作用,研究了不同的生化参数。此外,还对肾脏组织进行了组织病理学检查。
通过升高血清炎症标志物,包括肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和 C 反应蛋白(CRP),证实了纳米氧化锌诱导的肾毒性。此外,大鼠血清中的免疫球蛋白(IGg)、血管内皮生长因子(VEGF)和一氧化氮(NO)也显著增加。与对照组相比,n-ZnO 颗粒中毒的大鼠血清中尿素和肌酐水平也显著升高。此外,肾脏组织中的非酶抗氧化剂还原型谷胱甘肽(GSH)水平显著降低,血清葡萄糖水平升高。这些生化发现得到了肾脏组织的组织病理学检查的支持,该检查显示,在接受高剂量 n-ZnO 的动物中,许多肾小球发生萎缩和碎裂。此外,肾小管表现出上皮脱落、变性和坏死。一些肾小管的管腔中出现了管型。肾间质也观察到严重充血。这些影响是剂量依赖性的。用 Qur 和/或 Arg 与 n-ZnO 共同治疗大鼠可显著改善大多数偏离的测试参数。
数据表明,Qur 对 n-ZnO 氧化应激和相关血管并发症具有有益作用。此外,它与 Arg 的组合在改善纳米氧化锌肾毒性方面更为有效。