Wright E E, Bird J L, Feldman J M
Res Commun Chem Pathol Pharmacol. 1979 May;24(2):259-72.
Prior studies indicate that the monoamine oxidase inhibitors (MAOI) harmine and iproniazide inhibit N-acetyltransferase activity from liver. In this report we have demonstrated that harmine and harmaline are potent inhibitors of N-acetyltransferase, purified from hamster and rat liver. However, other MAOI such as deprenyl, clorgyline, methysergide, cyproheptadine, phenelzine, pargyline, methyltryptamine and tranylcypromine have either no effect, or only trivial effects on N-acetyltransferase. There is no correlation between a compound's properties as an MAO and N-acetyltransferase inhibitor. One must consider the inhibitory effect of harmine and harmaline on both MAO and N-acetyltransferase when evaluating the effects of these compounds on physiological processes.
先前的研究表明,单胺氧化酶抑制剂(MAOI)去氢骆驼蓬碱和异烟酰异丙肼可抑制肝脏中的N-乙酰基转移酶活性。在本报告中,我们已证明去氢骆驼蓬碱和骆驼蓬灵是从仓鼠和大鼠肝脏中纯化出来的N-乙酰基转移酶的有效抑制剂。然而,其他MAOI,如司来吉兰、氯吉兰、甲基麦角新碱、赛庚啶、苯乙肼、帕吉林、甲基色胺和反苯环丙胺对N-乙酰基转移酶要么没有影响,要么只有微不足道的影响。一种化合物作为MAO和N-乙酰基转移酶抑制剂的特性之间没有相关性。在评估这些化合物对生理过程的影响时,必须考虑去氢骆驼蓬碱和骆驼蓬灵对MAO和N-乙酰基转移酶的抑制作用。