东北农业大学学报
東北農業大學學報
동북농업대학학보
JOURNAL OF NORTHEAST AGRICULTURAL UNIVERSITY
2013年
2期
59-63
,共5页
徐雅琴%李静%于泽源%杨昱%于子淇
徐雅琴%李靜%于澤源%楊昱%于子淇
서아금%리정%우택원%양욱%우자기
黑穗醋栗%黄酮%抗氧化性%非酶糖基化反应
黑穗醋慄%黃酮%抗氧化性%非酶糖基化反應
흑수작률%황동%항양화성%비매당기화반응
black currant%flavonoids%antioxidant activity%non-enzymatic glycation reaction
文章考查黑穗醋栗总黄酮对羟基自由基(·OH)、超氧阴离子自由基(O2-·)以及DPPH自由基的清除能力,并通过NBT还原实验、二羰基化合物测定实验、非酶糖基化终产物的荧光性测定试验,研究黄酮对非酶糖基化反应三个阶段的抑制作用.结果表明,在黄酮浓度为1.0 mg·mL-1时,对羟自由基的清除率达到82.46%;浓度为0.8 mg·mL-1时,对超氧阴离子自由基的清除率达到81.33%;浓度为0.6 mg·mL-1时,对DPPH自由基清除率达到57.68%;对非酶糖基化反应三个阶段的抑制率分别为30.69%、48.15%、42.59%;黑穗醋栗总黄酮作为一种天然自由基清除剂,具有良好的抗氧化活性,同时也表现出一定的抗非酶糖基化活性.
文章攷查黑穗醋慄總黃酮對羥基自由基(·OH)、超氧陰離子自由基(O2-·)以及DPPH自由基的清除能力,併通過NBT還原實驗、二羰基化閤物測定實驗、非酶糖基化終產物的熒光性測定試驗,研究黃酮對非酶糖基化反應三箇階段的抑製作用.結果錶明,在黃酮濃度為1.0 mg·mL-1時,對羥自由基的清除率達到82.46%;濃度為0.8 mg·mL-1時,對超氧陰離子自由基的清除率達到81.33%;濃度為0.6 mg·mL-1時,對DPPH自由基清除率達到57.68%;對非酶糖基化反應三箇階段的抑製率分彆為30.69%、48.15%、42.59%;黑穗醋慄總黃酮作為一種天然自由基清除劑,具有良好的抗氧化活性,同時也錶現齣一定的抗非酶糖基化活性.
문장고사흑수작률총황동대간기자유기(·OH)、초양음리자자유기(O2-·)이급DPPH자유기적청제능력,병통과NBT환원실험、이탄기화합물측정실험、비매당기화종산물적형광성측정시험,연구황동대비매당기화반응삼개계단적억제작용.결과표명,재황동농도위1.0 mg·mL-1시,대간자유기적청제솔체도82.46%;농도위0.8 mg·mL-1시,대초양음리자자유기적청제솔체도81.33%;농도위0.6 mg·mL-1시,대DPPH자유기청제솔체도57.68%;대비매당기화반응삼개계단적억제솔분별위30.69%、48.15%、42.59%;흑수작률총황동작위일충천연자유기청제제,구유량호적항양화활성,동시야표현출일정적항비매당기화활성.
This study is to investigate the hydroxyl radical, superoxide anion radical and DPPH radical scavenging capacity of the flavonoids in black currant, and through NBT reductive assay, measurement of dicarbonyl compounds and the fluorescence of advanced glycation end products, the Inhibitory effect of flavonoids on the three periods of non-enzymatic glycation reaction were investigated. Results showed that the concentration was 1 mg·mL-1, the scavenging rate of hydroxyl radical reached 82.46%, the concentration was 0.8 mg·mL-1, the scavenging rate of superoxide radical was 81.33%, the concentration was 0.6 mg·mL-1, the scavenging rate of DPPH radical was 57.68%. The three stages of non-enzymatic glycosylation reaction inhibition rate was 30.69%, 48.15%, 42.59% respectively. Black currant flavonoids, as a kind of natural free radical scavenger, had good antioxidant activity, also showed certain inhibitory effects on the non-enzymatic glycation.