氧化铈纳米颗粒对铅中毒大鼠生化指标及组织病理学变化的影响

M. Hajinezhad, Shaghayegh Hajian Shahri, A. Rahdar, Hojjat Zamanian
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引用次数: 4

摘要

背景:本研究旨在探讨氧化铈纳米颗粒(cerium oxide nanoparticles, CeNPs)对醋酸铅毒性的潜在保护作用。材料与方法:将30只成年雄性Wistar大鼠随机分为3组,除正常对照组外,同时给予饮用水醋酸铅(1000mg /L)处理5周。对照组大鼠和阴性对照组大鼠均腹腔注射生理盐水。同时,第三组在给铅前1周腹腔注射剂量0.5 mg/kg的CeNPs,并继续给药。最后,按常规方法提取血清,并处死大鼠,取肝、心、睾丸、肾组织进行组织病理学检查。结果:铅处理组血清尿素氮(BUN)、肌酐、谷草转氨酶(AST)、丙氨酸转氨酶(ALT)、丙二醛(MDA)水平显著升高(P<0.01)。铅中毒大鼠血清乳酸脱氢酶(LDH)、谷丙转氨酶(AST)和谷丙转氨酶(ALT)水平较未给药的阴性对照组显著降低(P<0.01)。肝脏和肾脏组织病理检查显示铅致损伤、肝细胞坏死和肾小球硬化的迹象。治疗组铅致损伤的组织病理体征明显减少。脂质过氧化水平也低于阴性对照组(P<0.05)。结论:目前的实验研究证实了CeNPs对慢性铅中毒大鼠的保护作用;然而,需要更多的实验来评估可能的副作用和相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Cerium Oxide Nanoparticles on Biochemical Parameters and Histopathological Changes in Lead-Intoxicated Rats
Background: The present study was conducted to investigate the potential protective effect of cerium oxide nanoparticles (CeNPs) against lead acetate-induced toxicity. Materials and Methods: In this study, 30 adult male Wistar rats were randomly divided into three groups and treated simultaneously, except for the normal control, for 5 weeks with lead acetate in drinking water (1000 mg/L). Control rats and negative control rats received saline intraperitoneally. At the same time, the third group was treated with intraperitoneal injections of CeNPs at the dose of 0.5 mg/kg 1 week before lead administration, and continued with its administration. Finally, serum was obtained by the conventional methods and rats were sacrificed to obtain liver, heart, testis, and kidney tissue for histopathological examinations. Results: The lead-treated group showed significant increases in blood urea nitrogen (BUN), serum creatinine, serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), and malondialdehyde (MDA) levels (P<0.01). Lead-intoxicated rats treated with CeNPs showed a significant decrease in serum lactate dehydrogenase (LDH), AST, and ALT levels compared to the untreated negative control group (P<0.01). The histopathological examination of liver and kidney tissues showed signs of lead-induced injuries, necrotic hepatocytes, and glomerulosclerosis. The CeNPs-treated group showed noticeable reductions in histopathological signs of lead-induced injuries. Lipid peroxidation levels were also lower in CeNPs-treated rats than negative controls (P<0.05). Conclusion: The current experimental study proved the protective effects of CeNPs in rats exposed to chronic lead-induced toxicity; however, more experiments are required to evaluate the possible side effects and interactions.
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