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源自紫薯品种“绫紫”的二酰化花青素的降血糖作用可通过α-葡萄糖苷酶抑制作用实现。

Anti-hyperglycemic effect of diacylated anthocyanin derived from Ipomoea batatas cultivar Ayamurasaki can be achieved through the alpha-glucosidase inhibitory action.

作者信息

Matsui Toshiro, Ebuchi Sumi, Kobayashi Mio, Fukui Keiichi, Sugita Koichi, Terahara Norihiko, Matsumoto Kiyoshi

机构信息

Department of Bioscience and Biotechnology, Division of Bioresource and Bioenvironmental Sciences, Faculty of Agriculture, Graduate School of Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.

出版信息

J Agric Food Chem. 2002 Dec 4;50(25):7244-8. doi: 10.1021/jf025913m.

Abstract

To clarify a postprandial glucose suppression effect of diacylated anthocyanin with alpha-glucosidase (AGH) inhibitory activity, a single oral administration study of it in male 8-week-old Sprague-Dawley rats was performed. The diacylated anthocyanin used in this study was peonidin 3-O-[2-O-(6-O-E-feruloyl-beta-D-glucopyranosyl)-6-O-E-caffeoyl-beta-D-glucopyranoside]-5-O-beta-D-glucopyranoside isolated from storage roots of the purple sweet potato (Ipomoea batatas cv. Ayamurasaki), which showed a potent maltase inhibitory activity with an IC(50) value of 200 microM preferable to sucrase inhibition. When the diacylated anthocyanin (100 mg/kg) was administered following maltose (2 g/kg), a maximal blood glucose level (BGL) at 30 min was significantly decreased by 16.5% (P < 0.01) compared to vehicle. A minimum 10 mg/kg dose of the anthocyanin was necessary for the suppression of glycemic rise, and the ED(20) (69 mg/kg) was estimated to be approximately 30-fold lower than that of the therapeutic drug acarbose (ED(20) = 2.2 mg/kg). A reduction of serum insulin secretion was also observed corresponding to the decrease in BGL. No significant change in BGL was observed when sucrose or glucose was ingested, suggesting that the anti-hyperglycemic effect of the anthocyanin was achieved by maltase inhibition, not by sucrase or glucose transport inhibition at the intestinal membrane.

摘要

为阐明具有α-葡萄糖苷酶(AGH)抑制活性的二酰化花青素的餐后血糖抑制作用,在8周龄雄性Sprague-Dawley大鼠中进行了单次口服给药研究。本研究中使用的二酰化花青素是从紫甘薯(Ipomoea batatas cv. Ayamurasaki)的块根中分离得到的芍药素3-O-[2-O-(6-O-E-阿魏酰基-β-D-吡喃葡萄糖基)-6-O-E-咖啡酰基-β-D-吡喃葡萄糖苷]-5-O-β-D-吡喃葡萄糖苷,其对麦芽糖酶具有较强的抑制活性,IC(50)值为200μM,优于蔗糖酶抑制活性。在给予麦芽糖(2g/kg)后给予二酰化花青素(100mg/kg),与对照组相比,30分钟时的最大血糖水平(BGL)显著降低了16.5%(P<0.01)。抑制血糖升高至少需要10mg/kg剂量的花青素,估计其半数有效剂量(ED(20))为69mg/kg,约为治疗药物阿卡波糖(ED(20)=2.2mg/kg)的30分之一。同时观察到血清胰岛素分泌减少与BGL降低相对应。摄入蔗糖或葡萄糖时未观察到BGL有显著变化,这表明花青素的降血糖作用是通过抑制麦芽糖酶实现的,而不是通过抑制蔗糖酶或肠膜上的葡萄糖转运。

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