Nakata Asami, Koike Yuka, Matsui Hirofumi, Shimadad Tsutomu, Aburada Masaki, Yang Jinwei
Nat Prod Commun. 2014 Sep;9(9):1291-4.
The SIRT1 enzyme-stimulating and anti-glycation activities of Kaempferia parviflora extract and its main polymethoxyflavonoids were evaluated in vitro. K. parviflora extract elevated SIRT1 catalytic activity by eight- and 17-fold at 20 μg/mL and 100 μg/mL, respectively, compared with vehicle only. Two major polymethoxyflavonoids, 3,5,7,3',4'-pentamethoxyflavone (4) and 5,7,4'-trimethoxyflavone (5), were isolated from this extract and are four- and fivefold more potent than resveratrol, hitherto the strongest known natural SIRT1 activator. In addition, the anti-glycation activity of K. parviflora extract was observed to be seven times more effective than aminoguanidine, a clinical anti-diabetes drug. 3,5,7,3',4'-Pentamethoxyflavone (4) and 5,7,4'-trimethoxyflavone (5) showed the strongest anti-glycation activity among the tested polymethoxyflavonoids. Further comparison of the activity of these structurally related polymethoxyflavonoids revealed a possible structure-activity relationship, in particular, for the contribution of methoxy moieties.
在体外评估了小花山奈提取物及其主要多甲氧基黄酮对SIRT1酶的刺激活性和抗糖化活性。与仅使用溶剂相比,小花山奈提取物在20μg/mL和100μg/mL时分别将SIRT1催化活性提高了8倍和17倍。从该提取物中分离出两种主要的多甲氧基黄酮,即3,5,7,3',4'-五甲氧基黄酮(4)和5,7,4'-三甲氧基黄酮(5),它们的效力比白藜芦醇(迄今为止已知最强的天然SIRT1激活剂)分别高4倍和5倍。此外,观察到小花山奈提取物的抗糖化活性比临床抗糖尿病药物氨基胍高7倍。在测试的多甲氧基黄酮中,3,5,7,3',4'-五甲氧基黄酮(4)和5,7,4'-三甲氧基黄酮(5)表现出最强的抗糖化活性。对这些结构相关的多甲氧基黄酮活性的进一步比较揭示了一种可能的构效关系,特别是甲氧基部分的贡献。