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机构地区:[1]西北农林科技大学食品科学与工程学院,陕西杨凌712100
出 处:《食品科学》2014年第9期137-141,共5页Food Science
摘 要:目的:评价血根碱的体外抗氧化活性,为血根碱作为天然抗氧化剂的应用提供理论依据。方法:采用DPPH自由基清除法测定血根碱的体外抗氧化能力;采用Cu2+/H2O2和AAPH体系诱导牛血清白蛋白(bovine serum albumin,BSA)氧化损伤和羰基化损伤模型,研究血根碱对上述损伤的保护作用;采用TBA法分别测定血根碱对FeSO4诱导的大豆卵磷脂氧化损伤的抑制作用,及AAPH诱导的鲱鱼精DNA氧化损伤的抑制作用。结果:血根碱可有效清除DPPH自由基,且呈浓度依赖性,在100μmol/L时清除率为85.94%;1~100μmol/L的血根碱可显著保护Cu2+/H2O2及AAPH体系诱导的BSA损伤;10~100μmol/L的血根碱可显著保护由Cu2+/H2O2体系诱导的BSA蛋白羰基化,当浓度为0.1~100μmol/L时可显著保护由AAPH诱导的BSA蛋白羰基化;血根碱浓度在6.25~100μmol/L范围内均可显著抑制由FeSO4及AAPH诱导的大豆卵磷脂及鲱鱼精DNA的氧化损伤。结论:血根碱可有效清除自由基及保护蛋白氧化损伤和羰基化损伤,亦可显著抑制脂质及DNA氧化损伤。The purpose of this paper is to evaluate the in vitro antioxidant activity of sanguinarine (SAN). The 2,2-diphenyl- 1-picrylhydrazyl (DPPH) radical scavenging activity of SAN was measured, and the protective effect against oxidative damage and carbohylation of bovine serum albumin (BSA) induced in Cu2+/H2O2 and 2,2-azobis(2-amidinopropane dihydrochloride) (AAPH) system was examined. The 2-thio-barbituric acid (TBA) method was applied to determine the protective effect of SAN against FeSO4-induced oxidative damage of soy lecithin and AAPH-induced oxidative damage of herring sperm DNA. The results showed that SAN effectively removed DPPH free radicals in a dose-dependent manner, with a clearance rate of 85.94% at a concentration of 100 μmol/L. Adding 1 to 100 μmol/L SAN could significantly protect BSA against oxidative damage induced by Cu2+/H2O2 and AAPH system, and adding 10 to 100 μmol/L and 0.1 to 100 pmol/L SAN could significantly protect BSA against carbonylation damage induced by Cu2+/H2O2 and AAPH system, respectively. SAN significantly protected soy lecithin against FeSO4-induced oxidative damage and protect herring sperm DNA against AAPH-indueed oxidative damage in the range of 6.25-100 μmol/L. In conclusion, SAN can effectively scavenge free radicals, inhibit oxidative protein damage and carbonylation, and suppress lioid and DNA oxidative damage.
分 类 号:TS201.4[轻工技术与工程—食品科学]
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