Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran, Iran.
FEBS Lett. 2013 Mar 18;587(6):652-8. doi: 10.1016/j.febslet.2013.01.022. Epub 2013 Feb 1.
Flavonoids and their precursor trans-chalcone have been reported as inhibitors of mammalian alpha-amylase. With regard to this background, neohesperidin dihydrochalcone (NHDC) effect was investigated toward porcine pancreatic alpha-amylase (PPA), and found to be an activator of the enzyme. The maximal activation (up to threefold) was found to occur at 4.8mM of NHDC, which could be considered to have a high activation profile, with regard to the alpha and beta parameters (alpha<1<beta). NHDC is a non-essential activator of the enzyme and based on the results obtained from modeling tools, it is suggested to interact with PPA at a hydrophilic site located at the N-terminal, far from the active site of the enzyme.
类黄酮及其前体查尔酮已被报道为哺乳动物α-淀粉酶的抑制剂。鉴于此背景,研究了新橙皮苷二氢查尔酮(NHDC)对猪胰腺α-淀粉酶(PPA)的作用,结果发现它是该酶的激活剂。在 4.8mM 的 NHDC 下,可观察到最大激活(高达三倍),这可以被认为是具有高激活特性的,根据α和β参数(α<1<β)。NHDC 是非必需的酶激活剂,并且根据建模工具获得的结果,它被建议与位于 N 端的远离酶活性部位的亲水部位相互作用。