Inhibitory activities of prenylated flavonoids from Sophora flavescens against aldose reductase and generation of advanced glycation endproducts

被引:81
作者
Jung, Hyun Ah [1 ]
Yoon, Na Young [1 ]
Kang, Sam Sik [2 ]
Kim, Yeong Sik [2 ]
Choi, Jae Sue [1 ]
机构
[1] Pukyong Natl Univ, Div Food Sci & Biotechnol, Pusan 608737, South Korea
[2] Seoul Natl Univ, Coll Pharm, Dept Pharmaceut Sci, Seoul 151742, South Korea
关键词
D O I
10.1211/jpp.60.9.0016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Important targets for the prevention and treatment of diabetic complications include aldose reductase (AR) inhibitors (ARIs) and inhibitors of advanced glycation endproduct (AGE) formation. Here we evaluate the inhibitory activities of prenylated flavonoids isolated from Sophora flavescens, a traditional herbal medicine, on rat lens AR (RLAR), human recombinant AIR (HRAR) and AGE formation. Among the tested compounds, two prenylated chalcones - desmethylanhydroicaritin (1) and 8-lavandulylkaempferol (2) - along with five prenylated flavanones - kurarinol (8), kurarinone (9), (2S)-2'-methoxykurarinone (10), (2S)-3 beta, 7,4'-trihydroxy-5-methoxy-8-(gamma, gamma-dimethylally)-flavanone (11), and kushenol E (13) were potent inhibitors of RLAR, with IC50 values of 0.95, 3.80, 2.13, 2.99, 3.77, 3.63 and 7.74 mu M, respectively, compared with quercetin (IC50 7.73 mu M). In the HRAR assay, most of the prenylated flavonoids tested showed marked inhibitory activity compared with quercetin (IC50 2.54 mu M). In particular, all tested prenylated flavonols, such as desmethylanhydroicaritin (1, IC50 0.45 mu M), 8-lavandulylkaempferol (2, IC50 0.79 mu M) and kushenol C (3, IC50 0.85 mu M), as well as a prenylated chalcone, kuraridin (5, IC50 0.271 mu M), and a prenylated flavanone, (2S)-7,4'-dihydroxy-5-methoxy-8-(gamma, gamma-dimethylally)-flavanone (12, IC50 0.37 mu M), showed significant inhibitory activities compared with the potent AR inhibitor epalrestat (IC50 0.28 mu M). Interestingly, prenylated flavonoids 1 (IC50 104.3 mu g mL(-1)), 2 (IC50 132.1 mu g mL(-1)), 3 (IC50 84.6 mu g mL(-1)) and 11 (IC50 261.0 mu g mL(-1)), which harbour a 3-hydroxyl group, also possessed good inhibitory activity toward AGE formation compared with the positive control aminoguanidine (IC50 115.7 mu g mL(-1)). Thus, S. flavescens and its prenylated flavonoids inhibit the processes that underlie diabetic complications and related diseases and may therefore have therapeutic benefit.
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页码:1227 / 1236
页数:10
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