玉米丝提取物减轻对乙酰氨基酚引起的大鼠肝毒性

Enas Wans, Mohamed M. Ahmed, A. Mousa, Enas Tahoon, S. Orabi
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引用次数: 2

摘要

扑热息痛(acetaminophen- n- acetyl-p- aminphenol, PCM)是一种最常见的解热镇痛化合物,广泛用于治疗感冒、咳嗽、发烧、慢性疼痛、肌肉疼痛、偏头痛、痛经、头痛、背痛和牙痛。对乙酰氨基酚过量被认为是肝毒性的主要原因之一。本研究旨在探讨玉米丝甲醇提取物(CSME)对对乙酰氨基酚(APAP)诱导的肝毒性的保护作用。因此,本研究选取雄性Wistar白化大鼠40只,随机分为4组(n=10)。对照组;口服0.9%生理盐水。CSME组,口服CSME,每日400 mg/kg BW,连续5周;APAP组,单次口服APAP, 2g/kg BW;APAP+ CSME组,与CSME组一样口服CSME,随后与APAP组一样口服APAP单剂量。本研究结果显示,APAP可显著提高丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)活性。与对照组相比,APAP引起丙二醛(MDA)和一氧化氮(NO)浓度显著升高。然而,与对照组相比,CSME预处理使所有生化参数恢复到正常水平。综上所述,口服CSME通过其抗氧化保护机制保护大鼠抗APAP肝毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Corn Silk Extract attenuates Acetaminophen-induced Hepatotoxicity in Rats
Paracetamol (acetaminophen-N-acetyl-p-aminophenol, PCM), a most common antipyretic & analgesic compound is widely used for the treatment of cold, cough, fever, pain including chronic pain, muscular ache, migraine, menstrual cramps, headache, backache and toothache. Acetaminophen over dosage is considered as one of the major causes of hepatic toxicity. The current study aimed to investigate the protective effect of corn silk methanolic extract (CSME) against acetaminophen (APAP)-induced hepatic toxicity. Therefore, the present study was carried out on 40 male Wistar albino rats, which were randomly allocated into four groups (n=10). Control group; orally administered with 0.9% normal saline. CSME group, orally received CSME, 400 mg/kg BW daily for 5 weeks; APAP group , orally administered with a single dose of APAP, 2g/kg BW; APAP+ CSME group , orally administered with CSME as in CSME group, followed by a single oral dose of APAP as in APAP group. The results of this study revealed that APAP caused a significant elevation in alanine  transaminase (ALT) and aspartate transaminase (AST) activities. Also, APAP caused significant increases in of  malondialdehyde (MDA) and nitric oxide (NO) concentrations compared with control group. However, pre-treatment with CSME restored all biochemical parameters toward the normal levels as the control group. In conclusion, oral administration of CSME protected rats against APAP hepatic toxicity through its antioxidant protective mechanisms.
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