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α-Glucosidase Inhibitory Activities of Fatty Acids Purified from the Internal Organ of Sea Cucumber Stichopus japonicas

机译:刺参内部器官中脂肪酸纯化的α-葡萄糖苷酶抑制活性

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摘要

α-Glucosidase inhibitory activities of the various solvent fractions (n-hexane, CHCl_3, EtOAc, BuOH, and water) of sea cucumber internal organ were investigated. 1,3-Dipalmitolein (1) and cis-9-octadecenoic acid (2) with potent α-glucosidase inhibitory activity were purified from the n-hexane fraction of sea cucumber internal organ. IC_(50) values of compounds 1 and 2 were 4.45 and 14.87 μM against Saccharomyces cerevisiae α-glucosidase. These compounds mildly inhibited rat-intestinal α-glucosidase. In addition, both compounds showed a mixed competitive inhibition against S. cerevisiae α-glucosidase and were very stable at pH 2 up to 60 min. The K_1 values of compounds 1 and 2 were 0.48 and 1.24 μM, respectively. Therefore, the internal organ of sea cucumber might be a potential new source of α-glucosidase inhibitors suitably used for prevention of obesity and diabetes mellitus.
机译:研究了海参内部器官的各种溶剂组分(正己烷,CHCl_3,EtOAc,BuOH和水)的α-葡萄糖苷酶抑制活性。从海参内部器官的正己烷馏分中纯化出具有有效α-葡萄糖苷酶抑制活性的1,3-二棕榈油酸酯(1)和顺式-9-十八碳烯酸(2)。相对于酿酒酵母α-葡萄糖苷酶,化合物1和2的IC_(50)值为4.45和14.87μM。这些化合物轻度抑制大鼠肠内的α-葡萄糖苷酶。另外,两种化合物均显示出针对啤酒酵母α-葡糖苷酶的混合竞争性抑制作用,并且在pH 2下至60分钟都非常稳定。化合物1和2的K_1值分别为0.48和1.24μM。因此,海参的内脏器官可能是α-葡萄糖苷酶抑制剂的潜在新来源,适用于预防肥胖和糖尿病。

著录项

  • 来源
    《Journal of Food Science》 |2015年第6期|H841-H847|共7页
  • 作者

    T. H. Nguyen; S. M. Kim;

  • 作者单位

    Dept. of Marine Food Science and Technology, Gaugneung-Wonju Natl. Univ., 7 Jukheon-gil, Gangneung 210-702, Republic of Korea;

    Dept. of Marine Food Science and Technology, Gaugneung-Wonju Natl. Univ., 7 Jukheon-gil, Gangneung 210-702, Republic of Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    α-glucosidase; antidiabetes; fatty acid; internal organ; sea cucumber;

    机译:α-葡萄糖苷酶;抗糖尿病脂肪酸;内部器官海参;

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