Arai Y, Nakazato K, Kinemuchi H, Tadano T, Satoh N, Oyama K, Kisara K
Department of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Neuropharmacology. 1991 Jul;30(7):809-12. doi: 10.1016/0028-3908(91)90190-m.
Ifenprodil, which is clinically used as a cerebral vasodilator, inhibited rat brain type A (MAO-A) and type B (MAO-B) monoamine oxidase activity. It did not, however, affect rat lung semicarbazide-sensitive amine oxidase. The degree of inhibition of either form of MAO was not changed by 30 min preincubation of the enzyme preparations at 37 degrees C with ifenprodil. Modes of inhibition of MAO-A and MAO-B by ifenprodil were competitive towards oxidation of their respective substrates, 5-hydroxytryptamine and benzylamine, with Ki values of 75 microM for inhibition of MAO-A and 110 microM for inhibition of MAO-B.
艾芬地尔在临床上用作脑血管扩张剂,它能抑制大鼠脑内A型(MAO - A)和B型(MAO - B)单胺氧化酶的活性。然而,它对大鼠肺组织中氨基脲敏感胺氧化酶没有影响。在37℃下将酶制剂与艾芬地尔预孵育30分钟,MAO两种形式的抑制程度均未改变。艾芬地尔对MAO - A和MAO - B的抑制模式对其各自底物5 - 羟色胺和苄胺的氧化具有竞争性,抑制MAO - A的Ki值为75微摩尔,抑制MAO - B的Ki值为110微摩尔。