Lyles G A, Callingham B A
J Pharm Pharmacol. 1979 Nov;31(11):755-60. doi: 10.1111/j.2042-7158.1979.tb13652.x.
The specific actiivty of rat heart MAO, towards both tyramine and benzylamine as substrates, was found to increase with the age of the animal, and also after administration of (-)-thyroxine to young male rats. Conversely, enzyme activity was decreased in animals made hypothyroid by including 2-thiouracil in their diet. However, with both age and altered thyroid status, relatively greater changes in the deamination of tyramine rather than in that of benzylamine, were obtained. Clorgyline and deprenyl, used as inhibitors of rat heart MAO, indicated that tyramine is metabolized solely by MAO-A, whereas benzylamine is a substrate for both MAO-A and -B, and also a clorgyline- and deprenyl-resistant enzymic activity. The proportional contribution of MAO-A, -B and the clorgyline-resistant enzyme towards the total benzylamine deamination in the rat heart was found to vary with the age and with altered thyroid status of the animal in such a way that selective changes in the activity of MAO-A appear to be largely responsible for the overall changes in the specific activity of rat heart MAO which occur in response to these developmental factors.
以酪胺和苄胺为底物时,发现大鼠心脏单胺氧化酶(MAO)的比活性随动物年龄增长而增加,在给年轻雄性大鼠注射(-)-甲状腺素后也会增加。相反,在饮食中添加2-硫脲使动物甲状腺功能减退时,酶活性会降低。然而,随着年龄增长和甲状腺状态改变,酪胺脱氨基的变化相对大于苄胺脱氨基的变化。用作大鼠心脏MAO抑制剂的氯吉兰和司来吉兰表明,酪胺仅由MAO-A代谢,而苄胺是MAO-A和-B的底物,也是一种对氯吉兰和司来吉兰耐药的酶活性。发现MAO-A、-B和耐氯吉兰酶对大鼠心脏中苄胺总脱氨基的比例贡献随动物年龄和甲状腺状态改变而变化,以至于MAO-A活性的选择性变化似乎在很大程度上导致了大鼠心脏MAO比活性随这些发育因素而发生的总体变化。