Suppr超能文献

鞣花酸可预防丙烯酰胺诱导的 Wistar 大鼠肝毒性中的氧化应激、炎症和组织病理学改变。

Ellagic Acid Prevents Oxidative Stress, Inflammation, and Histopathological Alterations in Acrylamide-Induced Hepatotoxicity in Wistar Rats.

机构信息

Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran.

Research Center of Tropical and Infectious Diseases, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

J Diet Suppl. 2020;17(6):651-662. doi: 10.1080/19390211.2019.1634175. Epub 2019 Jul 25.

Abstract

The present study was designed to investigate the changes in rat liver tissue after administration of acrylamide (ACR) and ellagic acid (EA). The latter compound was applied for its strong antioxidant and anti-inflammatory properties. In the present study, 35 male Wistar rats were randomly divided into five equal groups. These groups were normal saline (NS), ACR (20 mg/kg), ACR + EA (10 and 30 mg/kg EA), and EA (30 mg/kg). At the end of the experiment, the rats were decapitated. Biochemical and histopathological studies were conducted on liver and serum samples. ACR administration significantly decreased hepatic GSH level, SOD, GPx, and CAT activity when compared to the NS group. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), nitric oxide (NO), protein carbonyl (PC), malondialdehyde (MDA), tumor necrosis factor alpha (TNF-α), and interleukin 1 beta (IL-1β) levels increased as a result of ACR administration. Administration of EA (more potently at a dose of 30 mg/kg) resulted in a significant reversal of biochemical, inflammatory, and hepatic markers in ACR-intoxicated rats. These biochemical and inflammatory disturbances were supported by histopathological observations of the liver. Our results indicate that EA might be useful for the treatment of the hepatotoxicity induced by ACR via ameliorative effects on biochemical, oxidative stress, and inflammatory indices.

摘要

本研究旨在探讨丙烯酰胺(ACR)和鞣花酸(EA)给药后大鼠肝组织的变化。后者因其强大的抗氧化和抗炎特性而被应用。在本研究中,35 只雄性 Wistar 大鼠被随机分为五组,分别为生理盐水(NS)组、ACR(20mg/kg)组、ACR+EA(10 和 30mg/kg EA)组和 EA(30mg/kg)组。实验结束时,大鼠断头处死。对肝和血清样本进行生化和组织病理学研究。与 NS 组相比,ACR 给药显著降低了肝组织中的 GSH 水平、SOD、GPx 和 CAT 活性。天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、碱性磷酸酶(ALP)、一氧化氮(NO)、蛋白羰基(PC)、丙二醛(MDA)、肿瘤坏死因子-α(TNF-α)和白细胞介素 1β(IL-1β)水平升高。EA(在 30mg/kg 剂量下更有效)给药可显著逆转 ACR 中毒大鼠的生化、炎症和肝标志物。这些生化和炎症紊乱得到了肝组织病理学观察的支持。我们的结果表明,EA 可能通过改善生化、氧化应激和炎症指标对 ACR 诱导的肝毒性具有治疗作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验