Steppeler A, Starke K
Naunyn Schmiedebergs Arch Pharmacol. 1980 Oct;314(1):13-6. doi: 10.1007/BF00498426.
Intra- and extraneuronal compartments of rat hearts were selectively labelled by perfusion with 3H-noradrenaline in the presence of corticosterone 87 microM or cocaine 30 microM, respectively. The subsequent outflow of 3H-compounds was examined. As little as 1 nM amezinium diminished the outflow of intraneuronally formed 3H-DOPEG. This effect was antagonized by cocaine. Amezinium 1 microM was necessary to diminish the outflow of extraneuronally formed 3H-DOPEG. This effect was not counteracted by corticosterone. The results indicate that amezinium is both a potent and, at low concentrations, selective inhibitor of intraneuronal MAO.
分别在存在87微摩尔皮质酮或30微摩尔可卡因的情况下,用3H-去甲肾上腺素灌注大鼠心脏,对神经内和神经外区域进行选择性标记。随后检测3H化合物的流出情况。低至1纳摩尔的阿美齐铵减少了神经内形成的3H-DOPEG的流出。这种作用被可卡因拮抗。需要1微摩尔阿美齐铵才能减少神经外形成的3H-DOPEG的流出。这种作用未被皮质酮抵消。结果表明,阿美齐铵是一种强效且在低浓度下对神经内单胺氧化酶具有选择性的抑制剂。