Bashandy PhD Mostafa M, Saeed Hanan E, Ahmed Walaa M S, Ibrahim Marwa A, Shehata Olfat
Department of Clinical Pathology, Faculty of Veterinary Medicine, Cairo University, Giza 12211, Egypt.
Department of Clinical Pathology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, Egypt.
Toxicol Res (Camb). 2022 Apr 1;11(2):339-347. doi: 10.1093/toxres/tfac009. eCollection 2022 Apr.
Cadmium (Cd) is a highly toxic heavy metal that adversely affects both human and animal health. Chronic cadmium exposure causes serious kidney damage. The current study investigated the protective role of cerium oxide nanoparticles (CeONPs) against cadmium chloride (CdCl)-induced renal injury.
One hundred and twenty male albino rats were divided into 6 equal groups. Group (C): considered as control group which was given distilled water orally. Group (NC and NC): rats were injected i.p. with nanoceria at a dose of (0.1 and 0.5 mg/kg b.wt), respectively, twice a week for 2 weeks starting at the 15th day of the study. Group (Cd): rats were received CdCl orally (10 mg/kg b.wt) daily for 28 days. Groups (Cd + NC and Cd + NC): rats were given CdCl orally (10 mg/kg b.wt) for 28 days and CeONPs by i.p. injection at a dose of (0.1 and 0.5 mg/kg b.wt), respectively, twice a week for 2 weeks started at the 15th day of the experiment.
The Cd group exhibited a significant increase in the serum levels of IL-1β, KIM-1, Cys-C, and β2-MG, downregulation of the antioxidant initiator genes such as Nrf-2, and up-regulation of apoptosis markers such as nibrin gene (NBN). Urine examination showed a high level of microalbuminuria, abnormal physical, chemical, and microscopical changes in comparison with control groups.
Remarkably, posttreatment with CeONPs showed significant improvement in kidney histopathological picture and relieved the alterations in kidney biomarkers, inflammatory markers, urine abnormalities, and expressions of different genes as Nrf-2 and NBN.
镉(Cd)是一种剧毒重金属,会对人类和动物健康产生不利影响。长期接触镉会导致严重的肾脏损伤。本研究调查了氧化铈纳米颗粒(CeONPs)对氯化镉(CdCl)诱导的肾损伤的保护作用。
120只雄性白化大鼠被分为6个相等的组。组(C):作为对照组,口服蒸馏水。组(NC和NC):从研究的第15天开始,大鼠分别以(0.1和0.5毫克/千克体重)的剂量腹腔注射纳米氧化铈,每周两次,共2周。组(Cd):大鼠每天口服CdCl(10毫克/千克体重),持续28天。组(Cd + NC和Cd + NC):大鼠口服CdCl(10毫克/千克体重)28天,并从实验的第15天开始,分别以(0.1和0.5毫克/千克体重)的剂量腹腔注射CeONPs,每周两次,共2周。
Cd组血清中IL-1β、KIM-1、Cys-C和β2-MG水平显著升高,抗氧化启动基因如Nrf-2下调,凋亡标志物如nibrin基因(NBN)上调。尿液检查显示微量白蛋白尿水平较高,与对照组相比,物理、化学和显微镜检查有异常变化。
值得注意的是,CeONPs治疗后肾脏组织病理学图像有显著改善,并缓解了肾脏生物标志物、炎症标志物、尿液异常以及不同基因如Nrf-2和NBN表达的改变。