Kaur Gurpreet, Jabbar Zoobi, Athar Mohammad, Alam M Sarwar
Department of Medical Elementology and Toxicology, Faculty of Science, Jamia Hamdard, Hamdard Nagar, New Delhi 110062, India.
Food Chem Toxicol. 2006 Jul;44(7):984-93. doi: 10.1016/j.fct.2005.12.001. Epub 2006 Jan 19.
Most pomegranate (Punica granatum Linn., Punicaceae) fruit parts are known to possess enormous antioxidant activity. The present study evaluated antioxidant and hepatoprotective activity of pomegranate flowers. Alcoholic (ethanolic) extract of flowers was prepared and used in the present study. The extract was found to contain a large amount of polyphenols and exhibit enormous reducing ability, both indicative of potent antioxidant ability. The extract showed 81.6% antioxidant activity in DPPH model system. The ability of extract to scavenge reactive oxygen species (ROS) and reactive nitrogen species (RNS) was tested and it was found to significantly scavenge superoxide (O(2)(.-)) (by up to 53.3%), hydrogen peroxide (H(2)O(2)) (by up to 30%), hydroxyl radicals (()OH) (by up to 37%) and nitric oxide (NO) (by up to 74.5%). The extract also inhibited (.)OH induced oxidation of lipids and proteins in vitro. These results indicated pomegranate flower extract to exert a significant antioxidant activity in vitro. The efficacy of extract was tested in vivo and it was found to exhibit a potent protective activity in acute oxidative tissue injury animal model: ferric nitrilotriacetate (Fe-NTA) induced hepatotoxicity in mice. Intraperitoneal administration of 9 mg/kg body wt. Fe-NTA to mice induced oxidative stress and liver injury. Pretreatment with pomegranate flower extract at a dose regimen of 50-150 mg/kg body wt. for a week significantly and dose dependently protected against Fe-NTA induced oxidative stress as well as hepatic injury. The extract afforded up to 60% protection against hepatic lipid peroxidation and preserved glutathione (GSH) levels and activities of antioxidant enzymes viz., catalase (CAT), glutathione peroxidase (GPX) glutathione reductase (GR) and glutathione-S-transferase (GST) by up to 36%, 28.5%, 28.7%, 40.2% and 42.5% respectively. A protection against Fe-NTA induced liver injury was apparent as inhibition in the modulation of liver markers viz., aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), bilirubin and albumin in serum. The histopathological changes produced by Fe-NTA, such as ballooning degeneration, fatty changes, necrosis were also alleviated by the extract. These results indicate pomegranate flowers to possess potent antioxidant and hepatoprotective property, the former being probably responsible for the latter.
众所周知,大多数石榴(石榴科石榴属植物石榴)果实部分具有强大的抗氧化活性。本研究评估了石榴花的抗氧化和肝脏保护活性。制备了石榴花的乙醇提取物并用于本研究。发现该提取物含有大量多酚,并具有强大的还原能力,这两者均表明其具有强大的抗氧化能力。该提取物在DPPH模型系统中显示出81.6%的抗氧化活性。测试了该提取物清除活性氧(ROS)和活性氮(RNS)的能力,发现它能显著清除超氧阴离子(O(2)(.-))(高达53.3%)、过氧化氢(H(2)O(2))(高达30%)、羟基自由基(()OH)(高达37%)和一氧化氮(NO)(高达74.5%)。该提取物还能在体外抑制(.)OH诱导的脂质和蛋白质氧化。这些结果表明石榴花提取物在体外具有显著的抗氧化活性。在体内测试了该提取物的功效,发现在急性氧化组织损伤动物模型:次氮基三乙酸铁(Fe-NTA)诱导的小鼠肝毒性中,它具有强大的保护活性。以50 - 150 mg/kg体重的剂量方案给小鼠腹腔注射9 mg/kg体重的Fe-NTA会诱导氧化应激和肝损伤。用石榴花提取物预处理一周,剂量为50 - 150 mg/kg体重,能显著且剂量依赖性地保护小鼠免受Fe-NTA诱导的氧化应激和肝损伤。该提取物对肝脂质过氧化的保护作用高达60%,并使谷胱甘肽(GSH)水平以及抗氧化酶即过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPX)、谷胱甘肽还原酶(GR)和谷胱甘肽-S-转移酶(GST)的活性分别保持在高达36%、28.5%、28.7%、40.2%和42.5%。对Fe-NTA诱导的肝损伤的保护作用表现为血清中肝标志物即天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、胆红素和白蛋白的调节受到抑制。Fe-NTA引起的组织病理学变化,如气球样变性、脂肪变性、坏死也被该提取物减轻。这些结果表明石榴花具有强大的抗氧化和肝脏保护特性,前者可能是后者的原因。