石榴肠道葡萄糖摄取抑制剂的分离。

H. Kim, S. Baek, H. Cho
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引用次数: 9

摘要

抑制肠道葡萄糖摄取有助于降低糖尿病患者的血糖水平。为了从天然来源中寻找有效的肠道葡萄糖摄取抑制剂,采用Caco-2细胞和荧光d -葡萄糖类似物2-[N-(7-硝基苯-2-氧-1,3-二唑-4-基)氨基]-2-脱氧d -葡萄糖(2- nbdg)筛选了70种本地食用植物、水果和蔬菜。从石榴木甲醇提取物中分离出一种抑制葡萄糖摄取的化合物,称为PG-1a。PG-1a是一种分子量为418的邻苯二甲酸二异壬基酯类化合物(PDE)。PG-1a对肠道葡萄糖摄取的抑制作用呈剂量依赖性,在100毫升条件下,抑制作用达到89%。此外,PG-1a的肠道葡萄糖摄取抑制作用比苯二嗪高1.2倍,苯二嗪是一种众所周知的葡萄糖摄取抑制剂。本研究提示PG-1a具有控制膳食葡萄糖吸收的作用,可有效改善糖尿病的病情,可作为一种可选的治疗和预防药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation of Intestinal Glucose Uptake Inhibitor from Punica granatum L.
Inhibition of intestinal glucose uptake is beneficial in reducing the blood glucose level for diabetes. To search for an effective intestinal glucose uptake inhibitor from natural sources, 70 native edible plants, fruits and vegetables were screened using Caco-2 cells and fluorescent D-glucose analog 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino]-2-deoxy-D-glucose (2-NBDG). A compound that was able to inhibit glucose uptake was isolated from methanol extract of Punica granatum L. and called PG-1a. PG-1a appears to be a phthalic acid-diisononyl ester-like compound (PDE) with molecular weight of 418. The inhibitory effect of PG-1a on intestinal glucose uptake was dose-dependent with 89% inhibition at 100 ㎍/㎖. Furthermore, the intestinal glucose uptake inhibitory effect of PG-1a was 1.2-fold higher than phlorizin, a well known glucose uptake inhibitor. This study suggests that PG-1a could play a role in controlling the dietary glucose absorption, and that PG-1a can effectively improve the diabetic condition, and may be used as an optional therapeutic and preventive agent.
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