Pharmacology Department, Faculty of Pharmacy, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Biochemistry Department, Faculty of Science-Al Faisaliah, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia.
J Biochem Mol Toxicol. 2018 Mar;32(3):e22040. doi: 10.1002/jbt.22040. Epub 2018 Feb 22.
The alleviative effects of two antioxidants, carnosine (Car) and melatonin (Mel), against titanium dioxide nanoparticles (TiO -NPs) toxicity-induced oxidative and inflammatory renal damage were examined in rats. Administration of these antioxidants along with TiO -NPs effectively reduced serum urea, uric acid, creatinine, glucose, tumor necrosis factor-α, interleukin-6, C-reactive protein, immunoglobulin G, vascular endothelial growth factor, and nitric oxide, as well as a significant amelioration of the decrease in glutathione levels in renal tissue was observed, compared to those in rats treated with TiO -NPs alone. The renoprotective properties of the antioxidants were confirmed by reduced intensity of renal damage as demonstrated by histological findings. In conclusion, Car and Mel play protective roles against TiO -NPs-induced renal inflammation and oxidative injury, likely due to their antioxidant and anti-inflammatory properties.
两种抗氧化剂肌肽(Car)和褪黑素(Mel)对二氧化钛纳米颗粒(TiO-NPs)毒性诱导的氧化和炎症性肾损伤的缓解作用在大鼠中进行了研究。与单独给予 TiO-NPs 相比,同时给予这些抗氧化剂可有效降低血清尿素、尿酸、肌酐、葡萄糖、肿瘤坏死因子-α、白细胞介素-6、C 反应蛋白、免疫球蛋白 G、血管内皮生长因子和一氧化氮水平,并显著改善肾组织中谷胱甘肽水平的降低。抗氧化剂的肾保护特性通过组织学发现的肾损伤强度降低得到证实。总之,Car 和 Mel 发挥了对抗 TiO-NPs 诱导的肾炎症和氧化损伤的保护作用,这可能归因于它们的抗氧化和抗炎特性。