Pirouzpanah Saeed, Hanaee Jalal, Razavieh Seyed-Vali, Rashidi Mohammad-Reza
School of Health and Nutrition, Tabriz University of Medical Sciences, Tabriz, Iran.
J Enzyme Inhib Med Chem. 2009 Feb;24(1):14-21. doi: 10.1080/14756360701841301.
Flavonoids are an important group of natural compounds that can interfere with the activity of some enzymes. In this study, effects of various flavonoids on aldehyde oxidase (AO) activity were evaluated in vitro. AO was partially purified from guinea pig liver. The effects of 12 flavonoids from three subclasses of flavon-3-ol, flavan-3-ol and flavanone on the oxidation of vanillin and phenanthridine as substrates of AO and xanthine as a substrate of xanthine oxidase (XO) were investigated spectrophotometrically. Among the 12 flavonoids, myricetin and quercetin were the most potent inhibitors of both AO and XO. In general, the oxidation of vanillin was more inhibited by flavonoids than that of phenanthridine. Almost all of the flavonoids inhibited AO activity more potently than XO, which was more evident with non-planner flavanols. A planner structure seems to be essential for a potent inhibitory effect and any substitution by sugar moieties reduces the inhibitory effects. This study could provide a new insight into AO natural inhibitors with potential to lead to some food-drug interactions.
黄酮类化合物是一类重要的天然化合物,能够干扰某些酶的活性。在本研究中,体外评估了各种黄酮类化合物对醛氧化酶(AO)活性的影响。AO从豚鼠肝脏中部分纯化。采用分光光度法研究了黄酮-3-醇、黄烷-3-醇和黄烷酮三个亚类中的12种黄酮类化合物对作为AO底物的香草醛和菲啶以及作为黄嘌呤氧化酶(XO)底物的黄嘌呤氧化的影响。在这12种黄酮类化合物中,杨梅素和槲皮素是AO和XO最有效的抑制剂。一般来说,黄酮类化合物对香草醛氧化的抑制作用比对菲啶的抑制作用更强。几乎所有的黄酮类化合物对AO活性的抑制作用都比对XO更强,非平面黄烷醇的这种情况更为明显。平面结构似乎是产生有效抑制作用所必需的,糖基的任何取代都会降低抑制作用。本研究可为AO天然抑制剂提供新的见解,这些抑制剂可能导致一些食物-药物相互作用。