El-Bahr S M
Department of Physiology, Biochemistry and Pharmacology (Biochemistry), College of Veterinary Medicine and Animal Resources, King Faisal University, P.O. Box 400, Al-Hufof, 31982, Saudi Arabia; Department of Biochemistry, Faculty of Veterinary Medicine, Alexandria University, Egypt.
Phytother Res. 2015 Jan;29(1):134-40. doi: 10.1002/ptr.5239. Epub 2014 Oct 8.
Twenty-eight rats were examined in a 5-week experiment to investigate the effect of curcumin on gene expression and activities of hepatic antioxidant enzymes in rats intoxicated with aflatoxin B1 (AFB1 ). The rats were divided into four groups. Rats in 1-4 groups served as control, oral curcumin treated (15 mg/kg body weight), single i.p. dose of AFB1 (3 mg/kg body weight) and combination of single i.p. dose of AFB1 with oral curcumin treated, respectively. AFB1 Liver damage and oxidative stress were evident in untreated AFB1 -intoxicated rats as indicated by a significant elevation in hepatic transaminases, elevation in lipid peroxide biomarkers (thiobarbituric acid reactive substances; TBARS), reduction of reduced glutathione (GSH) concentration, reduction in the activities of antioxidant enzymes namely catalase (CAT), total superoxide dismutase (SOD), glutathione peroxidase (GPX) and glutathione-S-transferase (GST) and down-regulation of gene expression of these antioxidant enzymes compared to control. Liver sections of rats intoxicated with AFB1 showed a disrupted lobular architecture, scattered necrotic cells and biliary proliferation. Administration of curcumin with AFB1 resulted in amelioration of AFB1 -induced effects compared to untreated AFB1 -intoxicated rats via an up-regulation of antioxidant enzyme gene expression, activation of the expressed genes and increase in the availability of GSH.
在一项为期5周的实验中,对28只大鼠进行了检查,以研究姜黄素对黄曲霉毒素B1(AFB1)中毒大鼠基因表达和肝脏抗氧化酶活性的影响。将大鼠分为四组。第1 - 4组大鼠分别作为对照组、口服姜黄素处理组(15毫克/千克体重)、单次腹腔注射AFB1组(3毫克/千克体重)以及单次腹腔注射AFB1与口服姜黄素联合处理组。与对照组相比,未处理的AFB1中毒大鼠出现明显的肝脏损伤和氧化应激,表现为肝转氨酶显著升高、脂质过氧化生物标志物(硫代巴比妥酸反应性物质;TBARS)升高、还原型谷胱甘肽(GSH)浓度降低、抗氧化酶即过氧化氢酶(CAT)、总超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPX)和谷胱甘肽 - S - 转移酶(GST)活性降低以及这些抗氧化酶基因表达下调。AFB1中毒大鼠的肝脏切片显示小叶结构破坏、散在坏死细胞和胆管增生。与未处理的AFB1中毒大鼠相比,姜黄素与AFB1联合给药通过上调抗氧化酶基因表达、激活表达的基因以及增加GSH的可用性,减轻了AFB1诱导的影响。