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沙枣叶提取物的致突变性、抗突变性和抗氧化活性。

Mutagenic, antimutagenic and antioxidant potency of leaf extracts from Nitraria retusa.

机构信息

Laboratory of Cellular and Molecular Biology, Faculty of Dental Medicine, Rue Avicenne, Monastir 5000, Tunisia.

出版信息

Food Chem Toxicol. 2010 Aug-Sep;48(8-9):2283-90. doi: 10.1016/j.fct.2010.05.061. Epub 2010 May 25.

Abstract

Four extracts were prepared from the leaves of Nitraria retusa; methanol, ethyl acetate, chloroform and hexane extracts. An assay for the ability of these extracts to prevent mutations induced by various oxidants in Salmonella typhimurium TA102 and TA 104 strains was conducted. These extracts from leaf parts of N. retusa showed no mutagenicity either with or without the metabolic enzyme preparation (microsome fraction). The highest protection against methylmethanesulfonate induced mutagenicity was observed with chloroform and methanol extracts with inhibition percentages of 44.93% (at 50 microg/plate in the presence of TA102 strain) and 38% (at 10 microg/plate in the presence of TA104 strain), respectively. Whereas Hexane and chloroform extracts reduced the mutagenicity induced by 2-aminoanthracene by 83.4% (using the S. typhimurium TA104 assay system) and 65.3% (using the S. typhimurium TA 102 assay system), respectively. Antioxidant activity of N. retusa extracts was determined by the ability of each extract to protect plasmid DNA against strand scission induced by hydroxyl radicals. Chloroform extract exhibited the highest ability to protect plasmid DNA against hydroxyl radical induced DNA damages and exhibited the highest antioxidant capacity, with 0.95mM trolox equivalent when tested by the ferric reducing/antioxidant method.

摘要

从白刺叶中制备了四种提取物;甲醇、乙酸乙酯、氯仿和正己烷提取物。对这些提取物在伤寒沙门氏菌 TA102 和 TA104 菌株中防止各种氧化剂诱导突变的能力进行了测定。这些来自白刺叶部分的提取物既没有在有或没有代谢酶制剂(微粒体部分)的情况下显示出致突变性。对甲磺酸甲酯诱导的致突变性的最高保护作用是用氯仿和甲醇提取物观察到的,抑制率分别为 44.93%(在 TA102 菌株存在的情况下为 50μg/板)和 38%(在 TA104 菌株存在的情况下为 10μg/板)。而正己烷和氯仿提取物分别将 2-氨基蒽诱发的致突变性降低了 83.4%(使用伤寒沙门氏菌 TA104 检测系统)和 65.3%(使用伤寒沙门氏菌 TA102 检测系统)。白刺叶提取物的抗氧化活性通过每种提取物保护质粒 DNA 免受羟基自由基引起的链断裂的能力来确定。氯仿提取物在保护质粒 DNA 免受羟基自由基诱导的 DNA 损伤方面表现出最高的能力,用铁还原/抗氧化法测定时,其抗氧化能力为 0.95mMtrolox 当量。

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