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姜黄素纳米粒改善顺铂诱导的大鼠肝毒性和肾毒性。

Curcumin nanoparticles ameliorate hepatotoxicity and nephrotoxicity induced by cisplatin in rats.

机构信息

Medical Physiology Department, National Research Centre, Giza, Egypt.

Pathology Department, National Research Centre, Giza, Egypt.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2020 Oct;393(10):1941-1953. doi: 10.1007/s00210-020-01888-0. Epub 2020 May 23.

Abstract

The present work was conducted to investigate the effect of curcumin nanoparticles (CUR NPs) on cisplatin-induced hepatotoxicty and nephrotoxicity in rats. Rats were divided randomly into the following: control, rats treated daily with CUR NPs (50 mg/kg body wt/day) for 14 days, rats treated with a single dose of cisplatin (12 mg/kg body wt, i.p), and rats treated with a single dose of cisplatin followed by a daily administration of CUR NPs for 14 days. Cisplatin-induced hepato- and nephrotoxicity were evaluated by histological examinations and biochemical analyses of liver and kidney functions. Cisplatin induced significant increases in the activities of aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase (ALP) and in the levels of bilirubin, urea, uric acid and creatinine. In addition, the levels of hepatic and renal lipid peroxidation (MDA), nitric oxide (NO), and serum tumor necrosis factor-α (TNF-α) increased significantly. However, cisplatin significantly decreased hepatic and renal reduced glutathione levels and renal Na/K-ATPase activity. Treatment with CUR NPs ameliorated almost all the biochemical changes induced by cisplatin and improved the histopathological alterations in liver and kidney. In conclusion, the present findings indicate that CUR NPs offered an effective protection against cisplatin-induced hepatotoxicity and nephrotoxicity through its antioxidant and anti-inflammatory properties.

摘要

本研究旨在探讨姜黄素纳米粒子(CUR NPs)对顺铂诱导的大鼠肝毒性和肾毒性的影响。大鼠随机分为以下几组:对照组、连续 14 天每天给予 CUR NPs(50mg/kg 体重)的 CUR NPs 处理组、单次腹腔注射顺铂(12mg/kg 体重)的顺铂处理组和单次腹腔注射顺铂后连续 14 天每天给予 CUR NPs 的 CUR NPs 处理组。通过组织学检查和肝功能、肾功能生化分析评估顺铂诱导的肝毒性和肾毒性。顺铂诱导的 AST、ALT 和 ALP 活性以及胆红素、尿素、尿酸和肌酐水平显著升高。此外,肝和肾的脂质过氧化(MDA)、一氧化氮(NO)和血清肿瘤坏死因子-α(TNF-α)水平也显著升高。然而,顺铂显著降低了肝和肾的还原型谷胱甘肽水平和肾 Na/K-ATPase 活性。CUR NPs 治疗改善了顺铂引起的几乎所有生化变化,并改善了肝和肾的组织病理学改变。总之,这些发现表明 CUR NPs 通过其抗氧化和抗炎特性对顺铂诱导的肝毒性和肾毒性提供了有效的保护。

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