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羊蹄甲叶中山柰酚-3,7-O-(α)-二鼠李糖苷的降血糖作用及抗氧化潜力

Hypoglycemic effect and antioxidant potential of kaempferol-3,7-O-(alpha)-dirhamnoside from Bauhinia forficata leaves.

作者信息

de Sousa Eliandra, Zanatta Leila, Seifriz Ilana, Creczynski-Pasa Tânia Beatriz, Pizzolatti Moacir Geraldo, Szpoganicz Bruno, Silva Fátima Regina Mena Barreto

机构信息

Departamento de Química, Centro de Ciências Físicas e Matemáticas, Campus Universitário, Bairro Trindade. Cx. Postal 5069, CEP 88040-970, Florianópolis, SC, Brazil.

出版信息

J Nat Prod. 2004 May;67(5):829-32. doi: 10.1021/np030513u.

Abstract

In vivo and in vitro treatments were carried out to investigate the effects of kaempferol-3,7-O-(alpha)-dirhamnoside (kaempferitrin), a major flavonoid compound of the n-butanol fraction from Bauhiniaforficata leaves, on serum glucose levels, as well as its antioxidant potential. Oral administration of kaempferitrin led to a significant hypoglycemic effect in normal and in alloxan-induced diabetic rats. In normal rats, blood glucose lowering was observed only with the higher dose of kaempferitrin (200 mg/kg) at 1 h after treatment. However, the hypoglycemic effect of kaempferitrin in diabetic rats was evident at all doses tested (50, 100, and 200 mg/kg), and this profile was maintained throughout the period studied for both higher doses. Additionally, in glucose-fed hyperglycemic normal rats, the kaempferitrin failed to decrease blood glucose levels. In vitro antioxidant properties or action against reactive oxygen species of this compound was also evaluated. The compound showed high reactivity with 1,1-diphenyl-2-picryl hydrazyl (DPPH), IC(50) of 84.0 +/- 7.8 microM, inhibited myeloperoxidase activity with K(0.5) = 86 +/- 9.9 microM, and decreased lipid peroxidation, induced by ascorbyl radical either in microsomes or in asolectin and phosphatidylcholine liposomes, with IC(50)'s of 320 +/- 14.1, 223 +/- 8.3, and 112 +/- 8.8 microM, respectively.

摘要

进行了体内和体外实验,以研究来自羊蹄甲叶正丁醇部位的主要黄酮类化合物山柰酚-3,7-O-α-二鼠李糖苷(山柰苷)对血清葡萄糖水平的影响及其抗氧化潜力。口服山柰苷对正常大鼠和四氧嘧啶诱导的糖尿病大鼠均有显著的降血糖作用。在正常大鼠中,仅在治疗后1小时给予较高剂量的山柰苷(200mg/kg)时观察到血糖降低。然而,山柰苷在糖尿病大鼠中的降血糖作用在所有测试剂量(50、100和200mg/kg)下均很明显,并且在研究期间,两种较高剂量的降血糖作用均得以维持。此外,在葡萄糖喂养的高血糖正常大鼠中,山柰苷未能降低血糖水平。还评估了该化合物的体外抗氧化特性或对活性氧的作用。该化合物与1,1-二苯基-2-苦基肼(DPPH)反应性高,IC50为84.0±7.8μM,抑制髓过氧化物酶活性,K0.5 = 86±9.9μM,并降低了由抗坏血酸自由基在微粒体或大豆卵磷脂和磷脂酰胆碱脂质体中诱导的脂质过氧化,IC50分别为320±14.1、223±8.3和112±8.8μM。

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