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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Extraction, chemical analysis of Angelica sinensis polysaccharides and antioxidant activity of the polysaccharides in ischemia-reperfusion rats
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Extraction, chemical analysis of Angelica sinensis polysaccharides and antioxidant activity of the polysaccharides in ischemia-reperfusion rats

机译:当归多糖的提取,化学分析及多糖的抗氧化活性

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Angelica sinensis polysaccharides were analyzed using high performance liquid chromatography (HPLC) and Fourier Transform Infrared (FT-IR). The major sugar of the polysaccharide was saccharose (18.55%); and the sugar constituted about 83% of the monomer content. Glucose and fructose were found as minor components of the polysaccharides. The FT-IR spectra of A. sinensis polysaccharides are used for determination of their structural features. The FT-IR spectrum of A. sinensis polysaccharides showed bands at 1641cm~(-1), 1415cm~(-1), 1050cm~(-1) and 926cm~(-1) characteristic for the carboxylic group. Absorptions at 2920-2930cm~(-1) are attributed to asymmetrical stretching vibration of CH_2-group. Medium stretch observed in the range 1650-1400cm~(-1) is assigned to C-C stretching of polysaccharides. Cardioprotective effects of A. sinensis polysaccharides were evaluated by using myocardial ischemia/reperfusion (IR) rats. A. sinensis polysaccharides treatment significantly reduced myocardial infarction size, enhanced CT-1 and antioxidant enzymes activity, downregulated caspase-12 mRNA expression in rats. The study strongly suggests the cardioprotective activity of A. sinensis polysaccharides in limiting ischemia-reperfusion induced myocardial injury.
机译:使用高效液相色谱(HPLC)和傅立叶变换红外(FT-IR)分析当归多糖。多糖中的主要糖是蔗糖(18.55%)。糖占单体含量的83%左右。发现葡萄糖和果糖是多糖的次要成分。中华曲霉多糖的FT-IR光谱用于确定其结构特征。中华曲霉多糖的FT-IR谱图显示了具有羧基特征的1641cm〜(-1),1415cm〜(-1),1050cm〜(-1)和926cm〜(-1)能带。 2920-2930cm〜(-1)处的吸收归因于CH_2基团的不对称拉伸振动。在1650-1400cm〜(-1)范围内观察到的中等拉伸被指定为多糖的C-C拉伸。通过使用心肌缺血/再灌注(IR)大鼠评估中华曲霉多糖的心脏保护作用。中华曲霉多糖治疗可显着降低大鼠心肌梗死面积,增强CT-1和抗氧化酶活性,下调caspase-12 mRNA表达。该研究强烈提示中华曲霉多糖在限制局部缺血再灌注引起的心肌损伤中的心脏保护活性。

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