Hendrickson H P, Sahafayen M, Bell M A, Kaufman A D, Hadwiger M E, Lunte C E
Department of Chemistry, University of Kansas, Lawrence 66045-0049.
J Pharm Biomed Anal. 1994 Mar;12(3):335-41. doi: 10.1016/0731-7085(94)90008-6.
The effect of several flavonoids on the benzene hydroxylase and phenol hydroxylase activity of rat hepatic microsomes was determined. The electrochemical characteristics of the flavonoids were also determined. The effect of flavonoids on microsomal phenol hydroxylase activity was found to correlate well with the oxidation potential for flavonoid aglycones. Easily oxidized flavonoids inhibited phenol hydroxylase activity with the extent of inhibition correlated to the ease of oxidation. This inhibition exhibited dose-dependent behaviour, with concentrations below 1 microM having no effect. On the other hand, flavonoids with high oxidation potentials increased phenol hydroxylase activity in a dose-independent manner. Hydroxyl substitution at C-7 was required for inhibition of phenol hydroxylase activity independently of the oxidation potential. Glycosylation at either C-7 or C-3 was found to moderate the inhibition of phenol hydroxylase activity. A linear relation was found between the degree of inhibition and the number of sugar residues for glycosylated flavonoids. There was no correlation between electrochemical properties and effect on microsomal benzene hydroxylase activity.
测定了几种黄酮类化合物对大鼠肝微粒体苯羟化酶和苯酚羟化酶活性的影响。还测定了黄酮类化合物的电化学特性。发现黄酮类化合物对微粒体苯酚羟化酶活性的影响与黄酮苷元的氧化电位密切相关。易氧化的黄酮类化合物抑制苯酚羟化酶活性,抑制程度与氧化难易程度相关。这种抑制表现出剂量依赖性,浓度低于1微摩尔/升时无作用。另一方面,具有高氧化电位的黄酮类化合物以剂量非依赖性方式增加苯酚羟化酶活性。无论氧化电位如何,C-7位的羟基取代是抑制苯酚羟化酶活性所必需的。发现C-7或C-3位的糖基化可减轻对苯酚羟化酶活性的抑制。对于糖基化黄酮类化合物,抑制程度与糖残基数量之间存在线性关系。电化学性质与对微粒体苯羟化酶活性的影响之间没有相关性。