首页> 外文期刊>Journal of medicinal food >Protective effects against H2O2-induced damage by enzymatic hydrolysates of an edible brown seaweed, sea tangle (Laminaria japonica).
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Protective effects against H2O2-induced damage by enzymatic hydrolysates of an edible brown seaweed, sea tangle (Laminaria japonica).

机译:对可食用棕色海藻、海缠结(海带)的酶水解物对 H2O2 诱导的损害的保护作用。

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摘要

Enzymatic hydrolysates of Laminaria japonica were evaluated for antioxidative activities using hydroxyl radical scavenging activity and protective effects against H(2)O(2)-induced DNA and cell damage. In addition, activities of antioxidative enzymes, including catalase, glutathione peroxidase, and glutathione S-transferase, of the enzymatic hydrolysates from L. japonica were also estimated. L. japonica was first enzymatically hydrolyzed by seven carbohydrases (Dextrozyme, AMG, Promozyme, Maltogenase, Termamyl, Viscozyme, and Celluclast all from Novo Co., Novozyme Nordisk, Bagsvaerd, Denmark) and five proteinases (Flavourzyme, Neutrase, Protamex, Alcalase all from Novo Co., and pancreatic trypsin). The hydroxyl radical scavenging activities of Promozyme and pancreatic trypsin hydrolysates from L. japonica were the highest as compared to those of the other carbohydrases and proteinases, and their 50 inhibitory concentration values were 1.67 and 317.49 mug/mL, respectively. The pancreatic trypsin hydrolysates of L. japonica exerted a protective effect on H(2)O(2)-induced DNA damage. We also evaluated the protective effect on hydroxyl radical-induced oxidative damage in PC12 cells via propidium iodide staining using a flow cytometer. The AMG and pancreatic trypsin hydrolysates of L. japonica dose-dependently protected PC12 cells against cell death caused by hydroxyl radical-induced oxidative damage. Additionally, we analyzed the activity of antioxidative enzymes such as catalase, glutathione peroxidase, and the phase II biotransformation enzyme glutathione S-transferase in L. japonica-treated cells. The activity of all antioxidative enzymes was higher in L. japonica-treated cells compared with the nontreated cells. These results indicate that enzymatic hydrolysates of L. japonica possess antioxidative activity.
机译:利用羟基自由基清除活性和对 H(2)O(2) 诱导的 DNA 和细胞损伤的保护作用,评估了海带的酶水解产物的抗氧化活性。此外,还估计了日本乳杆菌酶水解产物的抗氧化酶活性,包括过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽S-转移酶。粳乳杆菌首先由七种碳水化合物酶(右旋酶、AMG、Promozyme、麦芽糖酶、Termamyl、Viscozyme 和 Celluclast [均来自 Novo Co.、Novozyme Nordisk、Bagsvaerd、Denmark])和五种蛋白酶(Flavourzyme、Neutrase、Protamex、Alcalase [均来自 Novo Co.] 和胰腺胰蛋白酶)进行酶促水解。与其他糖水酶和蛋白酶相比,Promozyme和胰蛋白酶水解物的羟基自由基清除活性最高,其50%抑制浓度值分别为1.67和317.49 mug/mL。粳稻胰蛋白酶水解产物对H(2)O(2)诱导的DNA损伤具有保护作用。我们还通过使用流式细胞仪通过碘化丙啶染色评估了对 PC12 细胞中羟基自由基诱导的氧化损伤的保护作用。粳稻乳杆菌的AMG和胰蛋白酶水解产物剂量依赖性地保护PC12细胞免受羟基自由基诱导的氧化损伤引起的细胞死亡。此外,我们还分析了抗氧化酶(如过氧化氢酶、谷胱甘肽过氧化物酶和 II 期生物转化酶谷胱甘肽 S-转移酶)在粳稻乳杆菌处理的细胞中的活性。与未处理的细胞相比,粳稻乳杆菌处理的细胞中所有抗氧化酶的活性都更高。这些结果表明,日本乳杆菌的酶解产物具有抗氧化活性。

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