Department of Biology and Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay Road, Hong Kong SAR, China.
Chem Biol Interact. 2010 Sep 6;187(1-3):246-8. doi: 10.1016/j.cbi.2010.05.002. Epub 2010 May 7.
Acetylcholinesterase (AChE) inhibitors are widely used for the treatment of Alzheimer's disease (AD). Several AChE inhibitors, e.g. rivastigmine, galantamine and huperzine are originating from plants, suggesting that herbs could potentially serve as sources for novel AChE inhibitors. Here, we searched potential AChE inhibitors from flavonoids, a group of naturally occurring compounds in plants or traditional Chinese medicines (TCM). Twenty-one flavonoids, covered different subclasses, were tested for their potential function in inhibiting AChE activity from the brain in vitro. Among all the tested flavonoids, galangin, a flavonol isolated from Rhizoma Alpiniae Officinarum, the rhizomes of Alpiniae officinarum (Hance.) showed an inhibitory effect on AChE activity with the highest inhibition by over 55% and an IC(50) of 120 microM and an enzyme-flavonoid inhibition constant (K(i)) of 74 microM. The results suggest that flavonoids could be potential candidates for further development of new drugs against AD.
乙酰胆碱酯酶(AChE)抑制剂被广泛用于治疗阿尔茨海默病(AD)。几种 AChE 抑制剂,如利凡斯的明、加兰他敏和石杉碱甲,都源自植物,这表明草药可能是新型 AChE 抑制剂的潜在来源。在这里,我们从黄酮类化合物(植物或中药中天然存在的一组化合物)中寻找潜在的 AChE 抑制剂。我们测试了 21 种黄酮类化合物,涵盖了不同的亚类,以研究它们在体外抑制脑内 AChE 活性的潜在功能。在所有测试的黄酮类化合物中,从益智仁(Rhizoma Alpiniae Officinarum)根茎中分离得到的黄酮醇——高良姜素对 AChE 活性具有最强的抑制作用,抑制率超过 55%,IC50 为 120 μM,酶-黄酮类化合物抑制常数(K(i))为 74 μM。结果表明,黄酮类化合物可能是进一步开发治疗 AD 新药的潜在候选药物。