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首页> 外文期刊>Pharmacognosy magazine >In vitro and In vivo Antioxidant Activity of Flavonoid Extracted from Mulberry Fruit (Morus alba L.)
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In vitro and In vivo Antioxidant Activity of Flavonoid Extracted from Mulberry Fruit (Morus alba L.)

机译:桑Fruit中黄酮的体外和体内抗氧化活性

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Background: Many plants possess antioxidants that exhibit additive or synergistic activities. Objective: In this study, an ethanol-extracted flavonoid extracted from mulberry fruit (FEM) was evaluated for the antioxidant activity in vitro and the hemolysis in red blood cell (RBC) and lipid peroxidation in liver in vivo . Materials and Methods: Antioxidant activities in vitro were measured by quantifying its 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging activity, reducing power, and Fe2+-chelating ability. FEM inhibits hemolysis in RBCs and effects of lipid peroxidation in the liver were estimated. Results: The total content of flavonoid compounds was 187.23 mg of quercetin equivalents per grams dried material. In the in vitro assays, FEM demonstrated a strong antioxidant effect, especially in DPPH scavenging activity and reducing power. Mouse RBC hemolysis induced by H2O2 was significantly inhibited by FEM in a dose- and time-dependent manner. The effects of FEM on lipid peroxidation in liver, mitochondria, and microsome were investigated. The percentage of inhibition at high concentration (100 μg/mL) of FEM was 45.51%, 39.36%, and 42.78% for liver, mitochondria, and microsomes, respectively. These results suggest that the FEM possesses a strong antioxidant activity both in vivo and in vitro . SUMMARY The total content of flavonoid compounds in mulberry fruit was 187.23 mg/g dried material FEM showed a strong antioxidant effect, especially in 2,2-diphenyl-1-picrylhydrazyl scavenging activity and reducing power Mouse red blood cell hemolysis induced by H2O2 was significantly inhibited by FEM in a dose- and time-dependent manner The inhibition percentage at high concentration of FEM was 45.51%, 39.36%, and 42.78% for mouse’s liver, mitochondrial, and microsomes, respectively. Abbreviations used : FEM: Flavonoid Extracted from Mulberry fruit, H2O2: Hydrogen peroxide, DPPH: 2,2-diphenyl-1-picrylhydrazyl, EDTA: Ethylene diamine tetraacetic acid, MDA: malondialdehyde, TBA: 2-thiobarbituric acid, RBC: Red blood cells, DNJ: 1-deoxynojirimycin, LDL: low density lipoprotein, ROS: reactive oxygen species, EDTA2Na: Ethylenediaminetetraacetic acid disodium salt.
机译:背景:许多植物都具有抗氧化剂,这些抗氧化剂具有加和或协同作用。目的:本研究评估了从桑树果实中提取的乙醇提取的类黄酮(FEM)的体外抗氧化活性,体内红细胞的溶血(RBC)和肝脏脂质过氧化作用。材料与方法:通过定量测定其2,2-二苯基-1-吡啶并肼(DPPH)的清除活性,还原能力和Fe 2 + 螯合能力来测定其体外抗氧化活性。 FEM抑制了RBC中的溶血作用,并估计了肝脏中脂质过氧化作用。结果:每克干燥物料中类黄酮化合物的总含量为187.23 mg槲皮素当量。在体外测定中,FEM表现出很强的抗氧化作用,尤其是在DPPH清除活性和还原能力方面。 FEM显着抑制H 2 O 2 引起的小鼠RBC溶血,呈剂量和时间依赖性。研究了有限元法对肝脏,线粒体和微粒体脂质过氧化的影响。在高浓度(100μg/ mL)的FEM中,肝,线粒体和微粒体的抑制百分比分别为45.51%,39.36%和42.78%。这些结果表明,有限元在体内和体外都具有较强的抗氧化活性。总结桑果中黄酮类化合物的总含量为187.23 mg / g干物质FEM具有很强的抗氧化作用,尤其是在2,2-二苯基-1-吡啶并肼基清除活性和降低功率方面,H 2 O 2 的剂量和时间依赖性。高浓度FEM对小鼠肝脏的抑制率为45.51%,39.36%和42.78% ,线粒体和微粒体。使用的缩写词:FEM:从桑树果实中提取的类黄酮,H 2 O 2 :过氧化氢,DPPH:2,2-二苯基-1-吡啶并肼,EDTA:乙二胺四乙酸酸,MDA:丙二醛,TBA:2-硫代巴比妥酸,RBC:红细胞,DNJ:1-脱氧野oji霉素,LDL:低密度脂蛋白,ROS:活性氧,EDTA2Na:乙二胺四乙酸二钠盐。

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