Rat lens aldose reductase inhibitory constituents of Nelumbo nucifera stamens

被引:103
作者
Lim, Soon Sung
Jung, Yu Jung
Hyun, Sook Kyung
Lee, Yeon Sil
Choi, Jae Sue [1 ]
机构
[1] Pukyong Natl Univ, Fac Food Sci & Biotechnol, Pusan 608737, South Korea
[2] Hallym Univ, Silver Biotechnol Res Ctr, Chunchon 200702, South Korea
关键词
rat lens aldose reductase; Nelumbo nucifera Gaertn; kaempferol 3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-; beta-D-glucopyranoside; isorhamnetin 3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-glucopyranoside;
D O I
10.1002/ptr.1847
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
Aldose reductase, the principal enzyme of the polyol pathway, has been shown to play an important role in the complications associated with diabetes. A methanol extract of the stamens of Nelumbo nucifera Gaertn. was shown to exert an inhibitory effect on rat lens aldose reductase (RLAR), and thus was fractionated using several organic solvents, including dichloromethane, ethyl acetate and n-butanol. The ethyl acetate-soluble fraction, which manifested potent RLAR-inhibitory properties, was then purified further via repeated measures of silica gel and Sephadex LH-20 column chromatography. Thirteen flavonoids: kaempferol (1) and seven of its glycosides (2-9), myricetin 3',5'-dimethylether 3-O-beta-D-glueopyranoside (10), quercetin 3-O-beta-D-glucopyranoside (11) and two isorhamnetin glycosides (12, 13) were isolated from N. nucifera, as well as four non-flavonoid compounds: adenine (14), myo-inositol (15), arbutin (16) and beta-sitosterol glucopyranoside (17). These compounds were all assessed with regard to their RLAR-inhibitory properties. Among the isolated flavonoids, those harboring 3-O-alpha-L-rhamnopyranosyl-(I -> 6)-beta-D-glucopyranoside groups in their C rings, including kaempferol 3-O-alpha-L-rhamnopyranosyl-(I -> 6)-beta-D-glucopyranoside (5) and isorhamnetin 3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-glucopyranoside (13), were determined to exhibit the highest degree of rat lens aldose reductase inhibitory activity in vitro, evidencing IC50 values (concentration required for a 50% inhibition of enzyme activity) of 5.6 and 9.0 mu m, respectively. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:825 / 830
页数:6
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