首页> 外文期刊>ACS Omega >In Vitro Evaluation of Antidiabetic and Anti-Inflammatory Activities of Polyphenolic-Rich Extracts from Anchusa officinalis and Melilotus officinalis
【24h】

In Vitro Evaluation of Antidiabetic and Anti-Inflammatory Activities of Polyphenolic-Rich Extracts from Anchusa officinalis and Melilotus officinalis

机译:从嗜肺癌和Melilotus officinalis的多酚丰富的富含多酚醛提取物的抗糖尿病和抗炎活性的体外评价

获取原文
           

摘要

This study was focused on the phytochemical composition and biological activities of Anchusa officinalis and Melilotus officinalis polyphenolic-rich extracts obtained by nanofiltration. The high-performance liquid chromatography–mass spectrometry analysis showed that chlorogenic acid and rosmarinic acid were the main phenolic acids in both extracts. The main flavonoid compound from A. officinalis extracts is luteolin, whereas rutin and isoquercitrin are the main flavonoids in M. officinalis . M. officinalis polyphenolic-rich extract had the highest α-amylase (from hog pancreas) inhibitory activity (IC_(50) = 1.30 ± 0.06 μg/mL) and α-glucosidase (from Saccharomyces cerevisiae ) inhibitory activity (IC_(50) = 92.18 ± 1.92 μg/mL). However, both extracts presented a significant α-glucosidase inhibitory activity. Furthermore, the hyaluronidase inhibition of polyphenolic-rich extracts also proved to be stronger (IC_(50) = 11.8 ± 0.1 μg/mL for M. officinalis and 36.5 ± 0.2 μg/mL for A. officinalis ), but there was moderate or low lipoxygenase inhibition. The studies on the fibroblast cell line demonstrated that both A. officinalis and M. officinalis polyphenolic-rich extracts possess the cytotoxic effect at a concentration higher than 500 μg/mL. The experimental data suggest that both extracts are promising candidates for the development of natural antidiabetic and anti-inflammatory food supplements.
机译:本研究专注于通过纳米过滤获得的植物化学组合物和生物活性的植物化学组成和生物活性和 Melileotus Officinalis的多酚富含提取物。高效液相色谱 - 质谱分析表明,其两种提取物中的酚醛酸和玫瑰苷酸是主要的酚酸。来自 a的主要类黄酮化合物。 Officinalis萃取物是菱形,而芦丁和异喹蛋白是 m中的主要类黄酮。 officinalis。 m。富含Officinalis多酚的提取物具有最高的α-淀粉酶(来自猪胰腺)抑制活性(IC_(50)= 1.30±0.06μg/ ml)和α-葡糖苷酶(来自酿酒酵母)抑制活性(IC_(50) = 92.18±1.92μg/ ml)。然而,两种提取物呈现出显着的α-葡糖苷酶抑制活性。此外,富含多酚的富烯醇酶的透明质酸酶抑制也被证明是更强的(IC_(50)= 11.8±0.1μg/ ml,对于米。Officinalis和36.5±0.2μg/ ml为a。officinalis),但脂脂氧基酶抑制作用中度或低。成分细胞系的研究表明,两个 a。 officinalis和 m。 Officinalis丰富的富含细胞毒性效应高于500μg/ mL。实验数据表明,两种提取物都是对自然抗糖尿病和抗炎食品补充剂的开发的承诺候选人。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号