Department of Physics and Astronomy, College of Science, King Saud University, Riyadh, Saudi Arabia,
Int J Nanomedicine. 2018 Nov 21;13:7765-7770. doi: 10.2147/IJN.S183281. eCollection 2018.
This study aimed to evaluate the nephrotoxicity caused by gold nanoparticles (GNPs) and investigate the potential roles of quercetin (Qur) and arginine (Arg) in mitigating the inflammatory kidney damage and dysfunction and inhibiting the toxicity induced by GNPs in rats.
Kidney function was assessed using various serum biomarkers, including blood urea nitrogen (BUN), uric acid (URIC), and creatinine (CR), while toxicity was evaluated by measuring the biomarkers glutathione (GSH) and malondialdehyde (MDA) in kidney tissues.
Administration of GNPs to the rats severely affected the serum kidney biomarkers, as confirmed by the notable increases in BUN, URIC, and CR. Substantial changes in the levels of the biomarkers MDA and GSH in the kidney tissues were also observed, with a reduced level of GSH and elevated MDA activity. The administration of Qur or Arg exerted a protective effect against GNP-induced inflammatory kidney damage and toxicity, but with different responses according to their evaluated normalized values.
This study demonstrates the beneficial effects of supplementation with Qur or Arg during the treatment with GNPs, potentially providing a powerful tool for cancer therapy.
本研究旨在评估金纳米颗粒(GNPs)引起的肾毒性,并探讨槲皮素(Qur)和精氨酸(Arg)在减轻炎症性肾损伤和功能障碍以及抑制 GNPs 诱导的毒性方面的潜在作用。
通过各种血清生物标志物评估肾功能,包括血尿素氮(BUN)、尿酸(URIC)和肌酐(CR),同时通过测量肾组织中的谷胱甘肽(GSH)和丙二醛(MDA)等生物标志物来评估毒性。
GNPs 的给予严重影响了大鼠的血清肾生物标志物,BUN、URIC 和 CR 的显著增加证实了这一点。肾组织中 MDA 和 GSH 生物标志物水平也发生了显著变化,GSH 水平降低,MDA 活性升高。Qur 或 Arg 的给予对 GNP 诱导的炎症性肾损伤和毒性具有保护作用,但根据其评估的归一化值,反应不同。
本研究表明,在 GNPs 治疗期间补充 Qur 或 Arg 具有有益效果,可能为癌症治疗提供有力工具。