Kaur Gurpreet, Athar Mohammad, Alam M Sarwar
Department of Medical Elementology & Toxicology, Faculty of Science, Jamia Hamdard, Hamdard Nagar, New Delhi, India.
Chem Biol Interact. 2008 Feb 15;171(3):272-82. doi: 10.1016/j.cbi.2007.10.002. Epub 2007 Oct 22.
The present study reports the antioxidant activity of ethanolic extract of Quercus infectoria galls. The antioxidant potency of galls was investigated employing several established in vitro model systems. Their protective efficacy on oxidative modulation of murine macrophages was also explored. Gall extract was found to contain a large amount of polyphenols and possess a potent reducing power. HPTLC analysis of the extract suggested it to contain 19.925% tannic acid (TA) and 8.75% gallic acid (GA). The extract potently scavenged free radicals including DPPH (IC(50)0.5 microg/ml), ABTS (IC(50)1 microg/ml), hydrogen peroxide (H(2)O(2)) (IC(50)2.6 microg/ml) and hydroxyl (*OH) radicals (IC(50)6 microg/ml). Gall extract also chelated metal ions and inhibited Fe(3+) -ascorbate-induced oxidation of protein and peroxidation of lipids. Exposure of rat peritoneal macrophages to tertiary butyl hydroperoxide (tBOOH) induced oxidative stress in them and altered their phagocytic functions. These macrophages showed elevated secretion of lysosomal hydrolases, and attenuated phagocytosis and respiratory burst. Activity of macrophage mannose receptor (MR) also diminished following oxidant exposure. Pretreatment of macrophages with gall extract preserved antioxidant armory near to control values and significantly protected against all the investigated functional mutilations. MTT assay revealed gall extract to enhance percent survival of tBOOH exposed macrophages. These results indicate that Q. infectoria galls possess potent antioxidant activity, when tested both in chemical as well as biological models.
本研究报道了没食子的乙醇提取物的抗氧化活性。采用几种已建立的体外模型系统研究了没食子的抗氧化能力。还探讨了它们对小鼠巨噬细胞氧化调节的保护作用。发现没食子提取物含有大量多酚并具有强大的还原能力。提取物的高效薄层色谱分析表明其含有19.925%的鞣酸(TA)和8.75%的没食子酸(GA)。该提取物能有效清除自由基,包括二苯基苦味酰基自由基(DPPH)(半数抑制浓度(IC50)0.5微克/毫升)、2,2'-联氮-双-3-乙基苯并噻唑啉-6-磺酸(ABTS)(IC501微克/毫升)、过氧化氢(H2O2)(IC502.6微克/毫升)和羟基(·OH)自由基(IC506微克/毫升)。没食子提取物还能螯合金属离子,并抑制Fe(3+)-抗坏血酸诱导的蛋白质氧化和脂质过氧化。大鼠腹腔巨噬细胞暴露于叔丁基过氧化氢(tBOOH)会诱导其氧化应激并改变其吞噬功能。这些巨噬细胞显示溶酶体水解酶分泌增加,吞噬作用和呼吸爆发减弱。氧化剂暴露后巨噬细胞甘露糖受体(MR)的活性也降低。用没食子提取物预处理巨噬细胞可使抗氧化储备保持在接近对照值的水平,并显著保护细胞免受所有研究的功能损伤。噻唑蓝(MTT)法显示没食子提取物可提高tBOOH暴露巨噬细胞的存活率。这些结果表明,在化学和生物学模型中测试时,没食子具有强大的抗氧化活性。