Devor E J, Cloninger C R, Kwan S W, Abell C W
Department of Psychiatry, University of Iowa College of Medicine, Iowa City 52242-1057.
Alcohol Clin Exp Res. 1993 Apr;17(2):263-7. doi: 10.1111/j.1530-0277.1993.tb00760.x.
Platelet monoamine oxidase B (MAO B) activity and concentration were studied in a small sample of alcoholic families (n = 8) and in 20 unrelated, nonalcoholic controls. Complex segregation analyses of familial data indicated that both activity and concentration are controlled by a single major gene locus with a multifactorial background effect accounting for 0-50% of the variance. When the alcoholic family members (n = 24) were compared with the controls, all determinations of activity display significant differences, whereas MAO B concentration levels showed no difference. These results indicated that the lowered MAO B activities frequently reported among alcoholics do not reflect a change in the number of MAO B macromolecules expressed in platelets, but could be caused by the presence of an inhibitor or by a polymorphic or variant form of the enzyme.
在一小群酗酒家族样本(n = 8)和20名无亲缘关系的非酗酒对照者中,研究了血小板单胺氧化酶B(MAO B)的活性和浓度。对家族数据的复杂分离分析表明,活性和浓度均由一个主要基因位点控制,多因素背景效应占变异的0 - 50%。当将酗酒家族成员(n = 24)与对照者进行比较时,所有活性测定均显示出显著差异,而MAO B浓度水平则无差异。这些结果表明,酗酒者中经常报道的MAO B活性降低并不反映血小板中表达的MAO B大分子数量的变化,而是可能由抑制剂的存在或该酶的多态性或变异形式引起。