College of Veterinary Medicine, Jiangsu Key Laboratory of Zoonosis, Yangzhou University, Yangzhou, Jiangsu, 225009, China.
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu, 225009, China.
Environ Sci Pollut Res Int. 2017 Jan;24(2):1832-1844. doi: 10.1007/s11356-016-7953-x. Epub 2016 Oct 30.
Cadmium (Cd) is a toxic heavy metal that is widespread and nephrotoxic, but the mechanism of its toxicity is not well understood. Alpha-lipoic acid (α-LA) has a protective effect on Cd-induced oxidative stress, but the underlying mechanism is also not clear. This study aimed to confirm that Cd causes renal damage and to explore the potential underlying mechanism of α-LA to the kidney. Rats were randomly divided into four groups: control group, Cd group (50 mg/L CdAc), Cd+α-LA group (50 mg/L CdAc + 50 mg/kg body wt/day α-LA), and α-LA group (50 mg/kg body wt/day). The rats were exposed to Cd via drinking water and α-LA in the form of gavage at the same time every day. After 12 weeks, the activity of antioxidant enzymes and the level of Cd in the kidney were analyzed. Renal damage was evaluated based on histopathological and ultrastructure examinations. The apoptosis index was determined based on the results of western blotting and qRT-PCR. Our results indicate that accumulation of Cd causes serious kidney damage and α-LA has a protective effect against Cd-induced oxidative stress and apoptosis. Further, the findings indicate that the antioxidant, Cd chelation, and antiapoptotic activities of α-LA are the key factors that alleviate nephrotoxicity.
镉 (Cd) 是一种广泛存在且具有肾毒性的有毒重金属,但它的毒性机制尚不清楚。α-硫辛酸 (α-LA) 对 Cd 诱导的氧化应激具有保护作用,但潜在机制尚不清楚。本研究旨在证实 Cd 会造成肾脏损伤,并探讨 α-LA 对肾脏的潜在作用机制。大鼠随机分为四组:对照组、Cd 组(50mg/L CdAc)、Cd+α-LA 组(50mg/L CdAc+50mg/kg 体重/天 α-LA)和 α-LA 组(50mg/kg 体重/天)。大鼠通过饮水和灌胃同时每天暴露于 Cd 和 α-LA。12 周后,分析抗氧化酶的活性和肾脏中的 Cd 含量。根据组织病理学和超微结构检查评估肾损伤。根据 Western blot 和 qRT-PCR 的结果确定细胞凋亡指数。我们的结果表明,Cd 的积累会导致严重的肾脏损伤,而 α-LA 对 Cd 诱导的氧化应激和细胞凋亡具有保护作用。此外,研究结果表明,α-LA 的抗氧化、Cd 螯合和抗凋亡活性是减轻肾毒性的关键因素。